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        <title>Medical Microbiology and Immunology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Medical Microbiology and Immunology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Medical+Microbiology+and+Immunology&t=Medical+Microbiology+and+Immunology&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 21:35:07 +0100</lastBuildDate>
        <item>
            <title>Antiviral function and efficacy of polyvalent immunoglobulin products against CMV isolates in different human cell lines</title>
            <link>http://www.medworm.com/index.php?rid=5657246&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv061434547t850x6%2F</link>
            <description>This study suggests different antiviral
 functions of polyvalent IVIG and confirms their potential to inhibit a CMV infection in vitro, with profound differences between
 the hereby used IVIG products.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-10DOI 10.1007/s00430-012-0229-2Authors
		K. Frenzel, Institute of Medical Virology, Helmut-Ruska-Haus, Charité University Medicine, Charitéplatz 1, 10117 Berlin, GermanyS. Ganepola, Department of Haematology, Oncology and Transfusion Medicine, Charité University Medicine, Berlin, GermanyD. Michel, Institute of Virology, University Hospital Ulm, Ulm, GermanyE. Thiel, Department of Haematology, Oncology and Transfusion Medicine, Charité University Medicine, Berlin, GermanyD. H. Krüger, Institute of Medical Virology, Helmut-Ru...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5657246</comments>
            <pubDate>Wed, 01 Feb 2012 17:09:42 +0100</pubDate>
            <guid isPermaLink="false">5657246</guid>        </item>
        <item>
            <title>Correlation of partial env gene sequences with disease progression parameters in HIV-positive pregnant women from India</title>
            <link>http://www.medworm.com/index.php?rid=5636013&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh41657v13438h4kw%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ever since the beginning of the epidemic of HIV, one of the poignant aspects of HIV infection is transmission of the virus
 from mother to child. It is not known whether pregnancy accelerates the progression of HIV infection from a clinically asymptomatic
 stage to a progressive clinical phase. Present study was carried out to understand disease progression in pregnant women from
 India. We studied co-receptor utilization (the major determinant of HIV disease progression), N-glycosylation sites, and sequence
 variability. Blood samples were collected from 25 HIV sero-positive patients, eleven from the antenatal risk group (experimental group), nine from heterosexual male, and five from heterosexual female risk group (control group). Partial env gene was amplified by PCR...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5636013</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:39 +0100</pubDate>
            <guid isPermaLink="false">5636013</guid>        </item>
        <item>
            <title>Endogenous or exogenous spreading of HIV-1 in Nordrhein-Westfalen, Germany, investigated by phylodynamic analysis of the RESINA Study cohort</title>
            <link>http://www.medworm.com/index.php?rid=5625286&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7h0250xt6678770%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;HIV’s genetic instability means that sequence similarity can illuminate the underlying transmission network. Previous application
 of such methods to samples from the United Kingdom has suggested that as many as 86% of UK infections arose outside of the
 country, a conclusion contrary to usual patterns of disease spread. We investigated transmission networks in the Resina cohort,
 a 2,747 member sample from Nordrhein-Westfalen, Germany, sequenced at therapy start. Transmission networks were determined
 by thresholding the pairwise genetic distance in the pol gene at 96.8% identity. At first blush the results concurred with the UK studies. Closer examination revealed four large
 and growing transmission networks that encompassed all major transmission groups. One of th...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5625286</comments>
            <pubDate>Fri, 20 Jan 2012 07:07:01 +0100</pubDate>
            <guid isPermaLink="false">5625286</guid>        </item>
        <item>
            <title>Helicobacter pylori regulates iNOS promoter by histone modifications in human gastric epithelial cells</title>
            <link>http://www.medworm.com/index.php?rid=5569731&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqhx372252804j506%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Inducible nitric oxide synthase (iNOS) expression is altered in gastrointestinal diseases. Helicobacter pylori (Hp) infection may have a critical role in iNOS disregulation. We undertook this study to investigate possible chromatin changes
 occurring early during iNOS gene activation as a direct consequence of Hp–gastric cells interaction. We show that Hp infection is followed by different expression and chromatin modifications in gastric cells including (1) activation of iNOS
 gene expression, (2) chromatin changes at iNOS promoter including decreased H3K9 methylation and increased H3 acetylation
 and H3K4 methylation levels, (3) selective release of methyl-CpG-binding protein 2 from the iNOS promoter. Moreover, we show
 that Hp-induced activation of iNOS is delayed,...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5569731</comments>
            <pubDate>Wed, 04 Jan 2012 07:02:25 +0100</pubDate>
            <guid isPermaLink="false">5569731</guid>        </item>
        <item>
            <title>Febrile response induced by cecal ligation and puncture (CLP) in rats: involvement of prostaglandin E2 and cytokines</title>
            <link>http://www.medworm.com/index.php?rid=5556993&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx4811l627463tv43%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of the present study was to better understand the events involved in the febrile response induced by cecal ligation
 and puncture (CLP), a complex infectious process. To this end, we conducted in vivo experiments in rats examining (1) fever
 development, (2) bacterial number in the infection focus and in blood, (3) peripheral and hypothalamic synthesis of cytokines,
 (4) hypothalamic and cerebrospinal fluid (CSF) synthesis of prostaglandin E2 (PGE2), (5) the effect of anti-IL-6 antibody on fever, and (6) the effect of celecoxib on fever and hypothalamic synthesis of PGE2 after CLP induction. We found that CLP promotes fever and animal death depending on the number of punctures. The peak of
 CLP-induced fever overlapped with the maximal increase in the number...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5556993</comments>
            <pubDate>Tue, 27 Dec 2011 17:02:26 +0100</pubDate>
            <guid isPermaLink="false">5556993</guid>        </item>
        <item>
            <title>Control of M184V HIV-1 mutants by CD8 T-cell responses</title>
            <link>http://www.medworm.com/index.php?rid=5556995&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa145906h72435663%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Antiretroviral treatment directed against HIV is highly effective, yet limited by drug resistance mutations. We hypothesized
 that CD8 T cells targeting drug-resistant HIV mutants are able to inhibit viral replication in the setting of a failing therapeutic
 regimen. We evaluated CD8 T-cell responses and mapped epitopes in HIV-infected patients by interferon-gamma Elispot and intracellular
 cytokine staining. Autologous virus was sequenced by RT-PCR. Viral replication inhibition assays were performed using M184V
 mutant virus and CD8 T cell lines. CD8 T-cell responses toward the regions of viral drug resistance mutations in Pol are frequent.
 Focusing on the M184V mutation, A*02:01-YQYVDDLYV and A*02:01-VIYQYVDDLYV were identified as optimal epitopes for the majority
 o...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5556995</comments>
            <pubDate>Mon, 26 Dec 2011 16:46:57 +0100</pubDate>
            <guid isPermaLink="false">5556995</guid>        </item>
        <item>
            <title>Mutational patterns in the frameshift-regulating site of HIV-1 selected by protease inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=5556994&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft065522215gk8v60%2F</link>
            <description>In this study, we analysed the frameshift-regulating site of HIV-1 subtype B isolates, which
 also encodes for Gag and Pol proteins, classified as either treatment-naïve (TN) or protease inhibitor resistant (PI-R). HIV-1
 Gag cleavage site mutations (G435E, K436N, I437V, L449F/V) especially correlated with protease inhibitor resistance mutations,
 but also Pol cleavage site mutations (D05G, D05S) could be assigned to specific protease resistance profiles. Additionally,
 two Gag non-cleavage site mutations (S440F, H441P) were observed more often in HIV-1 isolates carrying protease resistance
 mutations. However, in dual luciferase assays, the frameshift efficiencies of specific clones did not reveal any effect from
 these mutations. Nevertheless, two patterns of mutations modestly increase...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5556994</comments>
            <pubDate>Mon, 26 Dec 2011 16:46:57 +0100</pubDate>
            <guid isPermaLink="false">5556994</guid>        </item>
        <item>
            <title>Seroprevalence study in forestry workers from eastern Germany using novel genotype 3- and rat hepatitis E virus-specific immunoglobulin G ELISAs</title>
            <link>http://www.medworm.com/index.php?rid=5520959&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6l371h5507175156%2F</link>
            <description>In this study, we tested four Escherichia coli-expressed segments of the capsid protein (CP) of a German wild boar-derived HEV genotype 3 strain for their diagnostic value
 in an indirect immunoglobulin G (IgG) ELISA. In an initial validation experiment, a carboxy-terminal CP segment spanning amino
 acid (aa) residues 326–608 outperformed the other segments harbouring aa residues 112–608, 326–660 and 112–335. Based on this
 segment, an indirect ELISA for detection of anti-HEV IgG antibodies in human sera was established and validated using a commercial
 line immunoassay as reference assay. A total of 563 sera from forestry workers of all forestry offices of Brandenburg, eastern
 Germany and 301 sera of blood donors from eastern Germany were surveyed using these assays. The commerci...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520959</comments>
            <pubDate>Sat, 17 Dec 2011 16:43:08 +0100</pubDate>
            <guid isPermaLink="false">5520959</guid>        </item>
        <item>
            <title>Immunopathology and Th1/Th2 immune response of Campylobacter jejuni-induced paralysis resembling Guillain–Barré syndrome in chicken</title>
            <link>http://www.medworm.com/index.php?rid=5437765&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgj542230331qkx8t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Immunopathogenesis of Campylobacter jejuni-associated Guillain–Barré syndrome (GBS) is not yet well established probably due to lack of experimental model. Therefore,
 we studied the Th1/Th2 immune response and pathological changes in C. jejuni-induced chicken model for GBS. C. jejuni (5&amp;nbsp;×&amp;nbsp;109 CFU/ml) and placebo were fed to 30 chickens each. Stools of all birds were negative for C. jejuni by culture and PCR before experiment. The birds were regularly assessed for disease symptoms up to 30&amp;nbsp;days. Sciatic nerves
 from all chickens were examined at 5&amp;nbsp;days intervals by histopathology and immunohistochemistry, and also for the expression
 of Th1/Th2 cytokines. Twenty-two chickens (73.3%) developed diarrhea after C. jejuni infection; 18 (60.0%) experim...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5437765</comments>
            <pubDate>Fri, 18 Nov 2011 17:34:41 +0100</pubDate>
            <guid isPermaLink="false">5437765</guid>        </item>
        <item>
            <title>Activation of cord blood myeloid dendritic cells by Trypanosoma cruzi and parasite-specific antibodies, proliferation of CD8+ T cells, and production of IFN-γ</title>
            <link>http://www.medworm.com/index.php?rid=5376597&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm74h616j50t30370%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We previously reported that Trypanosoma cruzi, the agent of Chagas disease, induces in congenitally infected fetuses a strong, adult-like parasite-specific CD8+ T cell response producing IFN-γ (Hermann et al. in Blood 100:2153–2158, 2002). This suggests that the parasite is able to overcome the immaturity of neonatal antigen presenting cells, an issue which
 has not been previously addressed. We therefore investigated in vitro the ability of T. cruzi to activate cord blood DCs and compared its effect to that on adult cells. We show that T. cruzi induces phenotypic maturation of cord blood CD11c+ myeloid DCs (mDCs), by enhancing surface expression of CD40, CD80, and CD83, and that parasite-specific IgG purified from
 cord blood of neonates born to T. cruzi-infected mo...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5376597</comments>
            <pubDate>Fri, 28 Oct 2011 17:13:36 +0100</pubDate>
            <guid isPermaLink="false">5376597</guid>        </item>
        <item>
            <title>Recent publications in medical microbiology and immunology: a retrospective</title>
            <link>http://www.medworm.com/index.php?rid=5376598&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm2314621w34k7w77%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A look back is done to some clinical and basic research activities recently published in medical microbiology and immunology.
 The review covers clinical experiences and in vitro experiments to understand the emergency, pathogenicity, epidemic spread,
 and vaccine-based prevention of avian and swine-origin flu. Some new developments and concepts in diagnosis, (molecular) epidemiology,
 and therapy of AIDS, viral hepatitis C, and herpesvirus-associated diseases are outlined. Regulation of immune system has
 been discussed in a special issue 2010 including some aspects of CNS affections (measles). Mycobacterial infection and its
 prevention by modern recombinant vaccines have reached new interest, as well as new concepts of vaccination and prophylaxis
 against several oth...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5376598</comments>
            <pubDate>Fri, 28 Oct 2011 05:49:41 +0100</pubDate>
            <guid isPermaLink="false">5376598</guid>        </item>
        <item>
            <title>Hepatitis E: are psychiatric patients on special risk?</title>
            <link>http://www.medworm.com/index.php?rid=5331389&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm65031837x615732%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hepatitis E virus (HEV) is largely confined to travelers returning from endemic areas, but the number of autochthonous cases
 of acute HEV infections in developed countries is increasing. Reservoirs for HEV are surface water, wild boar meat, and raw
 or undercooked pork meat. Usually, hepatitis E is a self-limiting disease presenting with acute hepatitis as a major clinical
 symptom. The seroprevalence of anti-HEV-IgG was investigated in 833 serum samples routinely collected from patients admitted
 to the university hospital in Frankfurt a. M., Germany (FFM) between 01.06.2008 and 31.12.2010. After determination of overall
 seroprevalence, we tested serum samples from patients diagnosed with acute elevation of liver enzymes (AELE), psychiatric
 (PSYCH), infectiological ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5331389</comments>
            <pubDate>Mon, 17 Oct 2011 16:04:55 +0100</pubDate>
            <guid isPermaLink="false">5331389</guid>        </item>
        <item>
            <title>Toll-like receptor-2 and interleukin-6 mediate cardiomyocyte protection from apoptosis during Trypanosoma cruzi murine infection</title>
            <link>http://www.medworm.com/index.php?rid=5311608&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F35108561nx177313%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Local innate immunity plays a key role in initiating and coordinating homeostatic and defense responses in the heart. We have
 previously reported that the cardiotropic parasite Trypanosoma cruzi, the etiological agent of Chagas disease, protects cardiomyocytes against growth factor deprivation-induced apoptosis. In
 this study, we investigated cardiomyocyte innate immune response to T. cruzi infection and its role in cellular protection from apoptosis. We found that Toll-like receptor (TLR) 2-expressing cells were
 strongly increased by the parasite in BALB/c neonatal mouse cardiomyocyte cultures. Using a dominant-negative system, we showed
 that TLR2 mediated cardiomyocyte survival and the secretion of interleukin (IL) 6, which acted as an essential anti-apoptotic
 fa...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5311608</comments>
            <pubDate>Sat, 08 Oct 2011 15:43:21 +0100</pubDate>
            <guid isPermaLink="false">5311608</guid>        </item>
        <item>
            <title>Human yeast-specific CD8 T lymphocytes show a nonclassical effector molecule profile</title>
            <link>http://www.medworm.com/index.php?rid=5257713&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw4n1516t30v46200%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pathogenic yeast and fungi represent a major group of human pathogens. The consequences of infections are diverse and range
 from local, clinically uncomplicated mycosis of the skin to systemic, life-threatening sepsis. Despite extensive MHC class
 I-restricted frequencies of yeast-specific CD8 T lymphocytes in healthy individuals and the essential role of the cell-mediated
 immunity in controlling infections, the characteristics and defense mechanisms of antifungal effector cells are still unclear.
 Here, we describe the direct analysis of yeast-specific CD8 T lymphocytes in whole blood from healthy individuals. They show
 a unique, nonclassical phenotype expressing granulysin and granzyme K in lytic granules instead of the major effector molecules
 perforin and granzy...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5257713</comments>
            <pubDate>Sat, 24 Sep 2011 15:47:38 +0100</pubDate>
            <guid isPermaLink="false">5257713</guid>        </item>
        <item>
            <title>No evidence for a role of xenotropic murine leukaemia virus-related virus and BK virus in prostate cancer of German patients</title>
            <link>http://www.medworm.com/index.php?rid=5204907&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe2w8143002717632%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Prostate cancer is one of the most prevalent types of cancer in men. Controversial data exist concerning the role of BKPyV
 and the xenotropic murine leukaemia virus-related gammaretrovirus (XMRV) in prostate cancer development. We therefore assessed
 the association between prostate cancer and viral infections. We could detect BKPyV in only 1 out of 85 prostate cancer samples,
 whereas none of the tissue samples showed evidence for XMRV positivity. Lack of detection of BKPyV and XMRV in prostate cancer
 tissues suggests that these viruses do not play a role in the pathogenesis of this type of cancer.
 
 
	Content Type Journal ArticleCategory Rapid CommunicationPages 1-4DOI 10.1007/s00430-011-0215-0Authors
		Baki Akgül, Institute of Virology, National Reference Center ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5204907</comments>
            <pubDate>Tue, 06 Sep 2011 15:42:55 +0100</pubDate>
            <guid isPermaLink="false">5204907</guid>        </item>
        <item>
            <title>The Campylobacter jejuni NCTC11168 capsule prevents excessive cytokine production by dendritic cells</title>
            <link>http://www.medworm.com/index.php?rid=5169214&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu417116161820p72%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Campylobacter jejuni is the leading cause of human bacterial gastroenteritis worldwide, mainly caused by handling and consumption of contaminated
 poultry. However, the immune response to infection is poorly understood. Here, the impact of the C. jejuni capsule, flagella and the N-linked glycosylation system on cytokine production by dendritic cells was investigated. Bone marrow-derived murine dendritic
 cells (BMDCs) infected with C. jejuni lacking the N-linked glycosylation system produced similar amounts of cytokines compared to cells infected with C. jejuni 11168H wild-type (WT) cultures. C. jejuni flagellin FlaA mutants elicited reduced IL-6 and IL-10 production in BMDCs compared to C. jejuni WT and this reduction was more pronounced in TLR4−/− BMDCs. An acap...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5169214</comments>
            <pubDate>Wed, 24 Aug 2011 07:19:34 +0100</pubDate>
            <guid isPermaLink="false">5169214</guid>        </item>
        <item>
            <title>Beta-papillomavirus DNA loads in hair follicles of immunocompetent people and organ transplant recipients</title>
            <link>http://www.medworm.com/index.php?rid=5076862&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Faq232r346w264158%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is increasing evidence of an association between human papillomaviruses (HPV) of the beta-genus (beta-PV) and the development
 of cutaneous squamous cell carcinoma (SCC). The viral DNA load may be an important determinant of pathogenicity, but there
 are currently no baseline epidemiological data relating to load in people without SCC. We investigated DNA-loads of eight
 beta-PV types previously associated with risk of SCC. We collected eyebrow hairs from immunocompetent people (ICP) and organ
 transplant recipients (OTR), determined load by quantitative PCR and obtained demographic, phenotypic, and sun exposure information.
 Viral loads for ICP from Australia (n&amp;nbsp;=&amp;nbsp;241) and Italy (n&amp;nbsp;=&amp;nbsp;223) and OTR from across Europe (n&amp;nbsp;=&amp;nbsp;318) spanned ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5076862</comments>
            <pubDate>Tue, 26 Jul 2011 15:50:38 +0100</pubDate>
            <guid isPermaLink="false">5076862</guid>        </item>
        <item>
            <title>Prevalence of hepatitis E virus-specific antibodies in humans with occupational exposure to pigs</title>
            <link>http://www.medworm.com/index.php?rid=5061672&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn833162447327r65%2F</link>
            <description>In this study, sera obtained from 24 slaughterers, 14 meat inspectors, 46 pig farmers and 22 veterinarians were tested
 for the presence of HEV-specific antibodies using a line immunoassay. For comparison, sera obtained from 116 age- and gender-matched
 blood donors were also included. Twenty eight per cent (28.3%; 30/106) of the swine-exposed humans and 15.5% (18/116) of the
 blood donors without contact to pigs exhibited IgG-antibodies determined as reactive (i.e. borderline or positive) against
 HEV. Thus, an increased risk of HEV infection in humans occupationally exposed to pigs and particularly for slaughterers (41.7%;
 10/24) was demonstrated.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00430-011-0210-5Authors
		Andi Krumbholz, Department of Virology and Antiviral Therapy...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5061672</comments>
            <pubDate>Tue, 19 Jul 2011 23:23:17 +0100</pubDate>
            <guid isPermaLink="false">5061672</guid>        </item>
        <item>
            <title>Probing of the nuclear import and export signals and subcellular transport mechanism of varicella-zoster virus tegument protein open reading frame 10</title>
            <link>http://www.medworm.com/index.php?rid=5048864&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F944640l284235771%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Varicella-zoster virus open reading frame 10 (ORF10), a tegument protein present in the virion, is a member of the alphaherpesvirus
 UL48 gene family that shares considerable amino acid sequence homology with the UL48 prototype, herpes simplex virus type
 1 VP16. VP16 serves multiple functions, including transcriptional activation of viral immediate-early genes. Furthermore,
 VP16 has been shown to be involved in some aspects of virus assembly and/or maturation. However, little is known concerning
 the function of ORF10. Here, we found that transient expression of ORF10 fused to enhanced yellow fluorescent protein (EYFP)
 in COS-7 cells showed the predominantly nuclear localization in the absence of other viral proteins. By constructing a series
 of ORF10 variants fused...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5048864</comments>
            <pubDate>Thu, 14 Jul 2011 06:01:58 +0100</pubDate>
            <guid isPermaLink="false">5048864</guid>        </item>
        <item>
            <title>Activation of MAPK/c-Fos induced responses in oral epithelial cells is specific to Candida albicans and Candida dubliniensis hyphae</title>
            <link>http://www.medworm.com/index.php?rid=4975026&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb571h3k17x132742%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oral epithelial cells detect the human pathogenic fungus Candida albicans via NF-κB and a bi-phasic mitogen-activated protein kinase (MAPK) signaling response. However, discrimination between C. albicans yeast and hyphal forms is mediated only by the MAPK pathway, which constitutes activation of the MAPK phosphatase MKP1 and
 the c-Fos transcription factor and is targeted against the hyphal form. Given that C. albicans is not the only Candida species capable of filamentation or causing mucosal infections, we sought to determine whether this MAPK/MKP1/c-Fos mediated
 response mechanism was activated by other pathogenic Candida species, including C. dubliniensis, C. tropicalis,
 C. parapsilosis, C. glabrata and C. krusei. Although all Candida species activated the NF-κB...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975026</comments>
            <pubDate>Fri, 24 Jun 2011 16:14:51 +0100</pubDate>
            <guid isPermaLink="false">4975026</guid>        </item>
        <item>
            <title>Rot and Agr system modulate fibrinogen-binding ability mainly by regulating clfB expression in Staphylococcus aureus NCTC8325</title>
            <link>http://www.medworm.com/index.php?rid=4975027&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp13617643856467l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Staphylococcus aureus is an important human pathogen that causes a variety of diseases, ranging from localized skin infections to life-threatening
 systemic infections. The success of S. aureus as a pathogen is partly due to its ability to adhere to a wide range of host tissues by binding to host extracellular matrix
 proteins such as fibrinogen, fibronectin, and collagen. Staphylococcus aureus expresses two proteins that can bind specifically to fibrinogen, clumping factors A and B (ClfA and ClfB). Repressor of toxins
 (Rot) is known to be a global regulator of virulence gene expression in S. aureus. The translation of Rot is regulated by the staphylococcal accessory gene regulator (Agr) quorum-sensing system. In this
 study, we demonstrated that Rot and the Agr syst...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975027</comments>
            <pubDate>Thu, 23 Jun 2011 16:29:54 +0100</pubDate>
            <guid isPermaLink="false">4975027</guid>        </item>
        <item>
            <title>Neurocysticercosis: local and systemic immune-inflammatory features related to severity</title>
            <link>http://www.medworm.com/index.php?rid=4975028&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq677k6k110jr514x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Neurocysticercosis (NC) is caused by the establishment of Taenia solium cysticerci in the central nervous system. Previous studies have established that neuroinflammation plays a key role in the
 severity of the disease. However, the relationship between peripheral and local immune response remains inconclusive. This
 work studies the peripheral and local immune-inflammatory features and their relationships, toward the identification of potential
 peripheral immunologic features related to severity. A panel of cytokines was measured in paired cerebrospinal fluid (CSF)
 and in the supernatant of antigen-specific stimulated peripheral blood mononuclear cells samples (SN) in a total of 31 untreated
 inflammatory and non-inflammatory NC patients. Increased clinical and radi...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975028</comments>
            <pubDate>Thu, 23 Jun 2011 06:02:37 +0100</pubDate>
            <guid isPermaLink="false">4975028</guid>        </item>
        <item>
            <title>Neuraminidase inhibitor susceptibility of swine influenza A viruses isolated in Germany between 1981 and 2008</title>
            <link>http://www.medworm.com/index.php?rid=4967945&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc3425782557777g5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;European swine influenza A viruses donated the matrix protein 2 as well as the neuraminidase (NA) gene to pandemic influenza
 A (H1N1) viruses that emerged in 2009. As a result, the latter became amantadine resistant and neuraminidase inhibitor (NAI)
 susceptible. These recent developments reflecting the close connection between influenza A virus infection chains in humans
 and pigs urge an antiviral surveillance within swine influenza A viruses. Here, NAI susceptibility of 204 serologically typed
 swine influenza A viruses of subtypes H1N1, H1N2, and H3N2 circulating in Germany between 1981 and 2008 was analyzed in chemiluminescence-based
 NA inhibition assays. Mean 50% inhibitory concentrations of oseltamivir and zanamivir indicate a good drug susceptibility
 of teste...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4967945</comments>
            <pubDate>Tue, 21 Jun 2011 18:00:24 +0100</pubDate>
            <guid isPermaLink="false">4967945</guid>        </item>
        <item>
            <title>High detection rate of Trichomonasvaginalis in benign hyperplastic prostatic tissue</title>
            <link>http://www.medworm.com/index.php?rid=4932915&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa24651j6lr076v5v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;While Trichomonas vaginalis, a protozoan parasite, is a well-investigated pathogen in the female population, there is little awareness of its significance
 in the male uro-genital tract. The presence of T. vaginalis in the prostate gland has only been scarcely investigated and has never been attested in conditions other than clinical prostatitis.
 Still, by some authors, this organ is regarded as ecologic niche for T. vaginalis. Since normal prostate tissue of sufficient quality is hard to come by, we investigated samples from 86 patients (mean age
 68.7&amp;nbsp;±&amp;nbsp;7.6&amp;nbsp;years) suffering from benign prostatic hyperplasia (BPH), a medical condition currently ranked as noninfectious,
 but characterized by chronic inflammatory tissue infiltrates of unknown etiology. A...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4932915</comments>
            <pubDate>Fri, 10 Jun 2011 06:41:52 +0100</pubDate>
            <guid isPermaLink="false">4932915</guid>        </item>
        <item>
            <title>A crucial role for IL-6 in the CNS of rats during fever induced by the injection of live E. coli</title>
            <link>http://www.medworm.com/index.php?rid=4920474&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7726u717733158n6%2F</link>
            <description>In conclusion, replicating E. coli promotes an integrated thermoregulatory response in which the central action of IL-6, but not IL-1 and TNF, appears to be
 important.
 
 
	Content Type Journal ArticlePages 1-14DOI 10.1007/s00430-011-0204-3Authors
		Denis M. Soares, Laboratory of Pharmacology, Department of Physic and Chemistry, University of São Paulo, Ribeirão Preto, São Paulo, BrazilMaria José Figueiredo, Laboratory of Pharmacology, Department of Physic and Chemistry, University of São Paulo, Ribeirão Preto, São Paulo, BrazilJuliano Manvailer Martins, Laboratory of Pharmacology, Department of Physic and Chemistry, University of São Paulo, Ribeirão Preto, São Paulo, BrazilRenes Resende Machado, Laboratory of Pharmacology, Department of Physic and Chemistry, University of São ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4920474</comments>
            <pubDate>Sun, 05 Jun 2011 05:45:26 +0100</pubDate>
            <guid isPermaLink="false">4920474</guid>        </item>
        <item>
            <title>Positive correlation between Merkel cell polyomavirus viral load and capsid-specific antibody titer</title>
            <link>http://www.medworm.com/index.php?rid=4901696&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fek7776w3735v14j3%2F</link>
            <description>In this study, we quantitated MCPyV DNA in skin swab specimens from healthy volunteers
 sampled at different anatomical sites over time periods ranging from 3&amp;nbsp;months to 4&amp;nbsp;years. The volunteers were also tested
 using a serological assay that detects antibodies specific for the MCPyV virion. There was a positive correlation between
 MCPyV virion-specific antibody titers and viral load at all anatomical sites tested (dorsal portion of the hands, forehead,
 and buttocks) (Spearman’s r 0.644, P&amp;nbsp;&amp;lt;&amp;nbsp;0.0001). The study results are consistent with previous findings suggesting that the skin is primary site of chronic MCPyV
 infection in healthy adults and suggest that the magnitude of an individual’s seroresponsiveness against the MCPyV virion
 generally reflects the overa...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4901696</comments>
            <pubDate>Wed, 25 May 2011 16:04:33 +0100</pubDate>
            <guid isPermaLink="false">4901696</guid>        </item>
        <item>
            <title>Seroprevalence study in forestry workers of a non-endemic region in eastern Germany reveals infections by Tula and Dobrava–Belgrade hantaviruses</title>
            <link>http://www.medworm.com/index.php?rid=4901697&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5x87656252353xvg%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Highly endemic and outbreak regions for human hantavirus infections are located in the southern, southeastern, and western
 parts of Germany. The dominant hantavirus is the bank vole transmitted Puumala virus (PUUV). In the eastern part of Germany,
 previous investigations revealed Tula virus (TULV) and Dobrava–Belgrade virus (DOBV) infections in the respective rodent reservoirs.
 Here, we describe a seroprevalence study in forestry workers from Brandenburg, eastern Germany, using IgG ELISA and immunoblot
 tests based on recombinant TULV, DOBV, and PUUV antigens. Out of the 563 sera tested, 499 from male and 64 from female workers,
 we found 41 out of the 499 (8.2%) sera from men (mean age 47&amp;nbsp;years) and 10 out of 64 (15.6%) from the women (mean age 48&amp;nbsp;years)...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4901697</comments>
            <pubDate>Tue, 24 May 2011 15:47:00 +0100</pubDate>
            <guid isPermaLink="false">4901697</guid>        </item>
        <item>
            <title>APOBEC3G/F as one possible driving force for co-receptor switch of the human immunodeficiency virus-1</title>
            <link>http://www.medworm.com/index.php?rid=4840176&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk063114475183302%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Human immunodeficiency virus-1 tropism highly correlates with the amino acid (aa) composition of the third hypervariable region
 (V3) of gp120. A shift towards more positively charged aa is seen when binding to CXCR4 compared with CCR5 (X4 vs. R5 strains),
 especially positions 11 and 25 (11/25-rule) predicting X4 viruses in the presence of positively charged residues. At nucleotide
 levels, negatively or uncharged aa, e.g., aspartic and glutamic acid and glycine, which are encoded by the triplets GAN (guanine-adenosine-any
 nucleotide) or GGN are found more often in R5 strains. Positively charged aa such as arginine and lysine encoded by AAR or
 AGR (CGN) (R means A or G) are seen more frequently in X4 strains suggesting our hypothesis that a switch from R5 to X4 strai...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4840176</comments>
            <pubDate>Sat, 14 May 2011 16:02:17 +0100</pubDate>
            <guid isPermaLink="false">4840176</guid>        </item>
        <item>
            <title>mTOR signaling pathway regulates the IL-12/IL-10 axis in Leishmania donovani infection</title>
            <link>http://www.medworm.com/index.php?rid=4840177&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh73084133057l068%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Leishmania-induced interleukin-12 (IL-12) expression is negatively regulated by the phosphatidylinositol 3-kinase (PI3K) and extracellular
 signal regulated kinase (ERK) 1/2 pathways in human monocyte derived macrophages (MDMs). To extend these studies, we examined
 the pathways downstream from PI3K in L. donovani-induced reciprocal regulation of IL-12/IL-10 axis in THP-1-derived macrophages. We show for the first time that in THP-1-derived
 macrophages and human monocytes, mTOR inhibition by rapamycin reversed L. donovani-induced IL-12 and IL-10 modulation. L. donovani-induced phosphorylation of P70S6K, a correlate of mTOR activity, in TLR-stimulated THP-1 derived macrophages. This increase
 in P70S6K phosphorylation was completely blocked by rapamycin (mTOR inhibito...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4840177</comments>
            <pubDate>Thu, 12 May 2011 16:44:55 +0100</pubDate>
            <guid isPermaLink="false">4840177</guid>        </item>
        <item>
            <title>The protective Th1 response in mice is induced in the T-cell zone only three weeks after infection with Leishmania major and not during early T-cell activation</title>
            <link>http://www.medworm.com/index.php?rid=4812415&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr2j88px3p0p65327%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The protozoan parasite Leishmania spp. causes clinical pictures ranging in severity from spontaneously healing skin ulcers to systemic disease. The immune
 response associated with healing involves the differentiation of IFNγ-producing Th1 cells, whereas the non-healing phenotype
 is associated with IL4-producing Th2 cells. The widespread assumption has been that the T-cell differentiation that leads
 to a healing or non-healing phenotype is established at the time of T-cell activation early after infection. By selectively
 analyzing the expression of cytokine genes in the T-cell zones of lymph nodes of resistant (Th1) C57BL/6 mice and susceptible
 (Th2) BALB/c mice during an infection with Leishmania major in vivo, we show that the early T-cell response does not diffe...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4812415</comments>
            <pubDate>Thu, 05 May 2011 16:36:32 +0100</pubDate>
            <guid isPermaLink="false">4812415</guid>        </item>
        <item>
            <title>Treatment with IP-10 induces host-protective immune response by regulating the T regulatory cell functioning in Leishmaniadonovani-infected mice</title>
            <link>http://www.medworm.com/index.php?rid=4779923&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0215347828017866%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Visceral leishmaniasis (VL), caused by the protozoan parasite, Leishmania
 donovani, is characterized by an infection in the liver and spleen. The failure of the first-line drugs has led to the development
 of new strategies for combating VL. Recently, our group has shown that interferon-γ-inducible protein (IP)-10, a CXC chemokine,
 renders protection against VL. In the present study, we have elucidated the mechanism by which IP-10 renders protection in
 in vivo
 L.
 donovani infection. We observed that IP-10–treated parasitized BALB/c mice showed a strong host-protective T helper cell (Th) 1 immune
 response along with marked decrease in immunosuppressive cytokines, tumor growth factor (TGF)-β, and interleukin (IL)-10 secreting
 CD4+ T cells. This IP-10-mediated d...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4779923</comments>
            <pubDate>Sat, 30 Apr 2011 23:39:47 +0100</pubDate>
            <guid isPermaLink="false">4779923</guid>        </item>
        <item>
            <title>Immune response in symptomatic and asymptomatic neurocysticercosis</title>
            <link>http://www.medworm.com/index.php?rid=4779924&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp7281gnu05427u56%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Innate immune system is crucial in the pathogenesis of neurocysticercosis (NCC) and helminth glycans can induce anti-inflammatory
 milieu via toll-like receptor 4 (TLR4) dependent mechanisms. The association of TLR4 and cytokines is yet to be explored in
 NCC. Therefore, the present study detected the serum levels of cytokines and soluble intercellular adhesion molecule (sICAM)-1
 in asymptomatic and symptomatic NCC and their association with TLR4 expression. Sixty eight patients with NCC (asymptomatic,
 36 and symptomatic, 32), and age and gender matched 37 healthy controls were enrolled to determine the levels of different
 pro- and anti-inflammatory cytokines, sICAM-1 in the serum by ELISA and expression of TLR4 in peripheral blood mononuclear
 cells (PBMCs) by flow ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4779924</comments>
            <pubDate>Sat, 30 Apr 2011 23:39:46 +0100</pubDate>
            <guid isPermaLink="false">4779924</guid>        </item>
        <item>
            <title>Specific detection of antibodies to different flaviviruses using a new immune complex ELISA</title>
            <link>http://www.medworm.com/index.php?rid=4779926&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx2n2g621830h1074%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Immune complex (IC) ELISAs for IgG antibodies to various virus antigens have turned out to be both highly specific and sensitive.
 During incubation of a labelled antigen with the serum samples, ICs are formed, which bind to microtiter plates coated with
 rheumatoid factor (RF) IgM. Here, we describe an improved coating of the solid-phase support comparing various Fc-receptor
 molecules. IC ELISAs were applied to detect human IgG antibodies to the highly virus-specific ED3 domain of West Nile- and
 tick-borne encephalitis virus envelopes. Compared with other Fc-receptor molecules like RF or C1q, FcγRIIA (CD32) turned out
 to bind the ICs composed of IgG antibodies and peroxidase-labelled ED3 antigens more efficiently. Due to low background reactions,
 sera could be tes...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4779926</comments>
            <pubDate>Sat, 30 Apr 2011 23:39:45 +0100</pubDate>
            <guid isPermaLink="false">4779926</guid>        </item>
        <item>
            <title>Screening and identification of host factors interacting with UL14 of herpes simplex virus 1</title>
            <link>http://www.medworm.com/index.php?rid=4753232&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F64721268627516k0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The UL14 protein of herpes simplex virus type 1 (HSV-1) is highly conserved in herpesvirus family. However, its exact function
 during the HSV-1 replication cycle is little known. In the present study, a high throughput yeast two-hybrid system was employed
 to screen the cellular factors interacting with UL14, and five target candidates were yielded: (1) TSC22 domain family protein
 3 (TSC22D3); (2) Mediator of RNA polymerase II transcription subunit 8 isoform 1(MED8); (3) Runt-related transcription factor
 3 (RUNX3); (4) Arrestin beta-2 (ARRB2); (5) Cereblon (CRBN). Indirect immunofluorescent assay showed that both TSC22D3 and
 MED8 co-localized with UL14. Co-immunoprecipitation assay demonstrated that UL14 could be immunoprecipitated by TSC22D3, suggesting
 that UL14 ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4753232</comments>
            <pubDate>Thu, 21 Apr 2011 17:58:22 +0100</pubDate>
            <guid isPermaLink="false">4753232</guid>        </item>
        <item>
            <title>The SnoB study: frequency of baseline raltegravir resistance mutations prevalence in different non-B subtypes</title>
            <link>http://www.medworm.com/index.php?rid=4696072&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr036r13705768776%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The SnoB study analysed the variability of the integrase (IN) gene of non-B viruses from treatment-naïve patients to determine
 whether non-B subtypes carry natural resistance mutations to raltegravir (RAL). Plasma viral RNA from 427 patients was gained,
 and IN sequences were subtyped and screened for subtype-specific highly-variable residues. Seven viruses of different subtypes
 were phenotypically tested for RAL susceptibility; 359/427 samples could be sequenced. One hundred and seventy samples (47%)
 were classified as non-B subtypes. No primary RAL resistance–associated mutations (RRAMs) were detected. Certain secondary
 mutations were found, mostly related to specific non-B subtypes. L74&amp;nbsp;M was significantly more prevalent in subtype 02_AG,
 T97A in A and 0...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4696072</comments>
            <pubDate>Thu, 07 Apr 2011 17:09:42 +0100</pubDate>
            <guid isPermaLink="false">4696072</guid>        </item>
        <item>
            <title>HIV prevalence and route of transmission in Turkish immigrants living in North-Rhine Westphalia, Germany</title>
            <link>http://www.medworm.com/index.php?rid=4683395&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu222qtg813271066%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The high number of Turkish immigrants in the German state North-Rhine Westphalia (NRW) compelled us to look for HIV-infected
 patients with Turkish nationality. In the AREVIR database, we found 127 (107 men, 20 women) Turkish HIV patients living in
 NRW. In order to investigate transmission clusters and their correlation to gender, nationality and self-reported transmission
 mode, a phylogenetic analysis including pol gene sequences was performed. Subtype distribution and the number of HIV drug
 resistance mutations in the Turkish patient group were found to be similar to the proportion in the non-Turkish patients.
 Great differences were observed in self-reported mode of transmission in the heterosexual Turkish male subgroup. Neighbour-joining
 tree of pol gene sequenc...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4683395</comments>
            <pubDate>Sat, 02 Apr 2011 05:56:39 +0100</pubDate>
            <guid isPermaLink="false">4683395</guid>        </item>
        <item>
            <title>Trypanosoma cruzi antigen immunization induces a higher B cell survival in BALB/c mice, a susceptible strain, compared to C57BL/6 B lymphocytes, a resistant strain to cardiac autoimmunity</title>
            <link>http://www.medworm.com/index.php?rid=4641947&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxv66613238124478%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chagas disease, caused by Trypanosoma cruzi, is endemic in Latin America and represents the most common infectious myocarditis worldwide. Autoimmunity is one of the
 mechanisms contributing to its pathogenesis. Although the cellular interactions that promote this autoimmune response are
 still poorly understood, several studies have demonstrated a key role for B lymphocytes since they secrete antibodies, cytokines
 and present antigens. Recently, we reported that immunization with cruzipain, an immunodominant T. cruzi antigen, induces a higher activation state in B cells from BALB/c mice (susceptible to cardiac autoimmunity) than B lymphocytes
 from C57BL/6 (a resistant strain). Here, we focused on the study of B cell survival in both mouse strains after cruzipain
 immu...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4641947</comments>
            <pubDate>Wed, 23 Mar 2011 16:56:37 +0100</pubDate>
            <guid isPermaLink="false">4641947</guid>        </item>
        <item>
            <title>Phenotypic and genetic characterization of varicella-zoster virus mutants resistant to acyclovir, brivudine and/or foscarnet</title>
            <link>http://www.medworm.com/index.php?rid=4559691&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm2x5180r6j39t165%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The treatment of varicella-zoster virus (VZV) reactivation is based on nucleoside analogues acyclovir (ACV) and bromevinyldeoxyuridine
 (BVdU) and a phosphonic acid derivative (PFA). Drug-resistant mutants of 3 wild-type (WT) VZV strains were obtained by exposure
 of human retinal pigment epithelial (hRPE) cells inoculated with cell-free WT virus at increasing concentrations of ACV, BVdU,
 and PFA. In addition to single-drug resistance, a cross-resistance of isolates vs. ACV was observed for PFA-resistant strains.
 Single-nucleotide (nt) exchanges resulting in amino acid (aa) substitutions were observed within the DNA polymerase (ORF 28)
 and/or thymidine kinase (ORF 36) of 3 of 3 ACV-, 2 of 3 BVdU-, and 3 of 3 PFA-resistant strains. Interestingly, aa substitutions
 wer...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4559691</comments>
            <pubDate>Fri, 04 Mar 2011 10:51:03 +0100</pubDate>
            <guid isPermaLink="false">4559691</guid>        </item>
        <item>
            <title>Conversion of Mycobacterium smegmatis to a pathogenic phenotype via passage of epithelial cells during macrophage infection</title>
            <link>http://www.medworm.com/index.php?rid=4540243&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7182353l4m04681%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mycobacteria encounter many different cells during infection within their hosts. Although alveolar epithelial cells play an
 essential role in host defense as the first cells to be challenged upon contact with mycobacteria, they may contribute to
 the acquisition of mycobacterial virulence by increasing the expression of virulence or adaptation factors prior to being
 ingested by macrophages on the side of pathogens. From this aspect, the enhanced virulence of nonpathogenic Mycobacterium smegmatis (MSM) passed through human alveolar A549 epithelial cells (A-MSM) was compared to the direct infection of MSM (D-MSM) in
 THP-1 macrophages and mouse models. The intracellular growth rate and cytotoxicity of A-MSM were significantly increased in
 THP-1 macrophages. In addition...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4540243</comments>
            <pubDate>Sat, 26 Feb 2011 21:42:10 +0100</pubDate>
            <guid isPermaLink="false">4540243</guid>        </item>
        <item>
            <title>Real-time PCR assay and a synthetic positive control for the rapid and sensitive detection of the emerging resistance gene New Delhi Metallo-β-lactamase-1 (blaNDM-1)</title>
            <link>http://www.medworm.com/index.php?rid=4540244&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3581h8tv13hhm8u3%2F</link>
            <description>We describe a real-time PCR assay as well as two conventional
 PCR assays to detect bla
 NDM-1. Only minute amounts of total DNA extracted from one bacterial colony are sufficient to allow detection of bla
 NDM-1 by real-time PCR within less than 1&amp;nbsp;h. We also introduce a chemically synthesized bla
 NDM-1 gene as a convenient positive control for those laboratories wishing to setup in-house assays for bla
 NDM-1 detection. Importantly, our study represents a proof of principle for the usefulness of rapidly synthesized genes serving
 as positive controls for novel diagnostic PCR assays of emerging pathogens during the initial phase after their discovery
 when biological isolates are still rare and not commonly available.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s00430-011-0...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4540244</comments>
            <pubDate>Thu, 24 Feb 2011 17:34:44 +0100</pubDate>
            <guid isPermaLink="false">4540244</guid>        </item>
        <item>
            <title>A DNA vaccine expressing CFP21 and MPT64 fusion protein enhances BCG-induced protective immunity against Mycobacterium tuberculosis infection in mice</title>
            <link>http://www.medworm.com/index.php?rid=4511885&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F42j1083369697086%2F</link>
            <description>In this study, we demonstrated that CFP21 and MPT64(rCM) fusion protein, encoded by RD2 of Mycobacterium tuberculosis, could stimulate higher level of interferon (IFN)-γ in tuberculin skin test (TST)-positive healthy population than in TST-negative
 healthy population. Compared with naive mice challenged with virulent M. tuberculosis H37Rv, C57BL/6 mice vaccinated with pcD2164 DNA expressing rCM protein resulted in a greater decrease in the bacterial load
 of lung. Moreover, pcD2164 could boost the protective immunity in mice primed by BCG than BCG alone or DNA vaccination alone,
 as evidenced by lower bacterial load in the lung tissue and reduced lung pathology. The protection induced by BCG prime-DNA
 vaccine boost strategy was associated with significant increases in rCM protein-specif...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4511885</comments>
            <pubDate>Mon, 21 Feb 2011 17:04:58 +0100</pubDate>
            <guid isPermaLink="false">4511885</guid>        </item>
        <item>
            <title>Do fewer cases of Kaposi’s sarcoma in HIV-infected patients reflect a decrease in HHV8 seroprevalence?</title>
            <link>http://www.medworm.com/index.php?rid=4501237&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb188645420633k22%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Infection with human herpes virus 8 (HHV8) is associated with development of Kaposi’s sarcoma (KS); therefore also known as
 KS-associated herpes virus. KS is closely associated with human immunodeficiency virus (HIV) infection, and consequently HHV8
 seroprevalence is higher in HIV-infected compared to HIV-negative patients. Currently, KS is rarely seen in clinical practice,
 which might be a consequence of an optimized anti-HIV treatment leading to an improved immunological status, or alternatively
 of a decrease in HHV8 prevalence. To determine the prevalence of HHV8 antibodies in HIV-positive compared to HIV-negative
 patients from the University Hospital Frankfurt/Main, Germany, and to compare our results with previously published data to
 illustrate trends in th...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4501237</comments>
            <pubDate>Fri, 18 Feb 2011 16:54:14 +0100</pubDate>
            <guid isPermaLink="false">4501237</guid>        </item>
        <item>
            <title>Significant increase in travel-associated dengue fever in Germany</title>
            <link>http://www.medworm.com/index.php?rid=4469990&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr83031778561n521%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Increasing numbers of dengue fever (DF) cases reflect the increasing travel mobility together with the expanding geographical
 distribution of the vector Aedes aegypti. Compared with earlier surveys in Germany, higher incidences occur and correlate
 well with ongoing outbreaks. Therefore, we investigated 767 serum samples from 594 returning travellers with suspected DF
 between 2005 and 2010, which where sent from different hospitals in the drainage area Frankfurt/Main. Established diagnostic
 assays were ELISA, immunofluorescence and chromatographic tests. We obtained 112 dengue-seropositive serum samples from totally
 60 patients: the detection rate was 10.1% (60 out of 594). A significant increase was found in 2010. Most patients were aged
 between 40 and 49, and ind...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4469990</comments>
            <pubDate>Thu, 10 Feb 2011 19:56:04 +0100</pubDate>
            <guid isPermaLink="false">4469990</guid>        </item>
        <item>
            <title>Analysis of Chlamydia pneumoniae infection in mononuclear cells by reverse transcription-PCR targeted to chlamydial gene transcripts</title>
            <link>http://www.medworm.com/index.php?rid=4428629&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa055k34724672364%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Chlamydia pneumoniae (C. pneumoniae) is an important etiological agent of respiratory infections including pneumonia. C. pneumoniae DNA can be detected in peripheral blood mononuclear cells indicating that monocytes can assist the spread of infection to
 other anatomical sites. Persistent infection established at these sites could promote inflammation and enhance pathology.
 Thus, the mononuclear cells are in a strategic position in the development of persistent infection. To investigate the intracellular
 replication and fate of C. pneumoniae in mononuclear cells, we have established an in vitro model in the human Mono Mac 6 cell line. In the present study, we analyzed
 the transcription of 11 C. pneumoniae genes in Mono Mac 6 cells during infection by real-time RT-P...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4428629</comments>
            <pubDate>Sat, 29 Jan 2011 17:17:53 +0100</pubDate>
            <guid isPermaLink="false">4428629</guid>        </item>
        <item>
            <title>The E2 protein of human papillomavirus type 8 increases the expression of matrix metalloproteinase-9 in human keratinocytes and organotypic skin cultures</title>
            <link>http://www.medworm.com/index.php?rid=4428630&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe43x41q748610127%2F</link>
            <description>In this report,
 we demonstrated by EMSA experiments that the MMP9 promoter contains a binding site for the transcriptional regulator E2 of
 HPV8. Transient reporter gene assays showed that HPV8-E2 activated the MMP9 promoter in a dose-dependent manner in human epidermal
 keratinocytes. An E2 transactivation-defective mutant (I73L) as well as a DNA-binding deficient mutant (R433K) demonstrated
 no activation of the MMP9 promoter, suggesting that both an intact transactivation and DNA-binding domain are required for
 E2 activation of the MMP9-promoter. The functional role of the E2 binding site within the MMP9 promoter was also confirmed
 by mutating the E2 binding site. In organotypic cultures of human skin, an overexpression of MMP9 was observed in suprabasal
 layers of the HPV8 E2-expres...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4428630</comments>
            <pubDate>Thu, 27 Jan 2011 17:37:05 +0100</pubDate>
            <guid isPermaLink="false">4428630</guid>        </item>
        <item>
            <title>Therapy of experimental influenza virus infection with pyrrolidine dithiocarbamate</title>
            <link>http://www.medworm.com/index.php?rid=4284883&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg752262745145w40%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The search for new antiviral strategies to treat influenza A virus (IAV) infections is one major international health care
 activity. Hereby, the IAV-caused misuse of cellular nuclear factor kappa B (NF-κB) signaling pathways in infected cells represents
 one target for antiviral therapy. In the present study, pyrrolidine dithiocarbamate (PDTC), which is known as an antioxidant
 and as an inhibitor of IAV-induced NF-κB activation, was studied in vivo. After the antiviral activity of PDTC was confirmed
 in MDCK cells, mice—infected with the mouse-adapted strain of IAV A/PR/8/34 (H1N1)—were treated intraperitoneally simultaneously
 with PDTC (75, 150, 200&amp;nbsp;mg/kg body weight). The influence of PDTC administrations was evaluated on viral replication and inflammato...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4284883</comments>
            <pubDate>Mon, 20 Dec 2010 22:05:54 +0100</pubDate>
            <guid isPermaLink="false">4284883</guid>        </item>
        <item>
            <title>Pyrosequencing allows the detection of emergent ganciclovir resistance mutations after HCMV infection</title>
            <link>http://www.medworm.com/index.php?rid=4275017&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe1563036103w370l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Prenatally acquired human cytomegalovirus (HCMV) infection is the most frequent viral infection of newborns in developed countries.
 Virostatic therapy is accompanied by side effects and stepwise emergence of resistant virus variants. Different genotypic
 approaches show limited sensitivity in detecting on-growing minor resistant virus populations. Here, we demonstrate the superiority
 of pyrosequencing for the monitoring of mutant emergence. In a preterm baby born after 28&amp;nbsp;weeks of gestation and suffering
 from disseminated congenital HCMV infection, long-term control could not be achieved under ganciclovir/valganciclovir therapy
 and the infant died on the 113th day of life. Resistance-associated mutations in the HCMV UL97 gene were not detected by conventional
 ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4275017</comments>
            <pubDate>Thu, 16 Dec 2010 18:24:41 +0100</pubDate>
            <guid isPermaLink="false">4275017</guid>        </item>
        <item>
            <title>Monitoring prevalence of varicella-zoster virus clades in Germany</title>
            <link>http://www.medworm.com/index.php?rid=4164210&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv451772432860035%2F</link>
            <description>In conclusion, almost one half of VZV infections in Germany were caused currently by VZV clade 3. In
 primary VZV infection, nearly 20% of clade 1 has been replaced by clade 5 that might spread more effectively in the population
 than the European VZV clades.
 
 
	Content Type Journal ArticleDOI 10.1007/s00430-010-0178-6Authors
		A. Sauerbrei, Institute of Virology and Antiviral Therapy, Jena University Hospital, Hans-Knoell- Strasse 2, 07745 Jena, GermanyJ. Stefanski, Institute of Virology and Antiviral Therapy, Jena University Hospital, Hans-Knoell- Strasse 2, 07745 Jena, GermanyA. Philipps, Institute of Virology and Antiviral Therapy, Jena University Hospital, Hans-Knoell- Strasse 2, 07745 Jena, GermanyA. Krumbholz, Institute of Virology and Antiviral Therapy, Jena University Hospital, ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4164210</comments>
            <pubDate>Fri, 12 Nov 2010 08:49:24 +0100</pubDate>
            <guid isPermaLink="false">4164210</guid>        </item>
        <item>
            <title>Erratum to: Prevalence and characteristics of hepatitis B and C virus infections in treatment-naïve HIV-infected patients</title>
            <link>http://www.medworm.com/index.php?rid=4142516&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftq60089n26503561%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s00430-010-0179-5Authors
		Stefan Reuter, Clinic of Gastroenterology, Hepatology and Infectious Diseases, University Hospital, Moorenstr. 5, 40225 Duesseldorf, GermanyMark Oette, Clinic of General Medicine, Gastroenterology and Infectious Diseases, Augustinerinnen Hospital, Cologne, GermanyFrank Clemens Wilhelm, Institute of Virology, University of Cologne, Cologne, GermanyBastian Beggel, Max Planck Institute for Informatics, Computational Biology and Applied Algorithmics, Saarbruecken, GermanyRolf Kaiser, Institute of Virology, University of Cologne, Cologne, GermanyMelanie Balduin, Institute of Virology, University of Cologne, Cologne, GermanyFinja Schweitzer, Institute of Virology, University of Cologne, Cologne, GermanyJens Verheyen, Institute ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4142516</comments>
            <pubDate>Thu, 04 Nov 2010 17:48:08 +0100</pubDate>
            <guid isPermaLink="false">4142516</guid>        </item>
        <item>
            <title>Oncomodulation by human cytomegalovirus: novel clinical findings open new roads</title>
            <link>http://www.medworm.com/index.php?rid=4096548&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F589g307172253473%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The question whether human cytomegalovirus may affect cancer diseases has been discussed (very controversially) for decades.
 There are convinced believers and strict opponents of the idea that HCMV might be able to play a role in the course of cancer
 diseases. In parallel, the number of published reports on the topic is growing. Recently published and presented (Ranganathan
 P, Clark P, Kuo JS, Salamat S, Kalejta RF. A Survey of Human Cytomegalovirus Genomic Loci Present in Glioblastoma Multiforme
 Tissue Samples. 35th Annual International Herpes Workshop, Salt Lake City, 2010) data on HCMV detection in glioblastoma tissues
 and colocalisation of HCMV proteins with cellular proteins known to be relevant for glioblastoma progression motivated us
 to recapitulate the cu...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4096548</comments>
            <pubDate>Thu, 21 Oct 2010 17:15:03 +0100</pubDate>
            <guid isPermaLink="false">4096548</guid>        </item>
        <item>
            <title>Current knowledge on PB1-F2 of influenza A viruses</title>
            <link>http://www.medworm.com/index.php?rid=4085855&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0h0vx8t073141815%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Almost 10&amp;nbsp;years ago, an eleventh protein of influenza A viruses was discovered in a search for CD8+ T-cell epitopes. This
 protein was named PB1-F2 since it is encoded in the +1 reading frame of the PB1 gene segment. Various studies have shown that
 PB1-F2 has a pleiotropic effect: (1) The protein can induce apoptosis in a cell type-dependent manner, (2) PB1-F2 is able
 to promote inflammation, and (3) finally it up-regulates viral polymerase activity by its interaction with the PB1 subunit.
 These properties could contribute to an enhanced pathogenicity. However, the underlying mechanism is not fully understood
 yet. New data suggest that some effects of PB1-F2 are strain-specific and host-specific.
 
 
	Content Type Journal ArticleDOI 10.1007/s00430-010-0176-8Aut...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4085855</comments>
            <pubDate>Sat, 16 Oct 2010 08:35:55 +0100</pubDate>
            <guid isPermaLink="false">4085855</guid>        </item>
        <item>
            <title>Characterization of the subcellular localization of herpes simplex virus type 1 proteins in living cells</title>
            <link>http://www.medworm.com/index.php?rid=4085856&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F78t540412501hh6h%2F</link>
            <description>In this study, we presented the construction of a library of expression clones for the herpes simplex virus type 1 (HSV-1)
 proteome and subcellular localization map of HSV-1 proteins in living cells using yellow fluorescent protein (YFP) fusion
 proteins. As a result, 21 proteins showed cytoplasmic or subcytoplasmic localization, 16 proteins showed nuclear or subnuclear
 localization, and others were present both in the nucleus and cytoplasm. Interestingly, most capsid proteins showed enriched
 or exclusive localization in the nucleus, and most of the envelope proteins showed cytoplasmic localization, suggesting that
 subcellular localization of the proteins correlated with their functions during virus replication. These results present a
 subcellular localization map of HSV-1 proteins in...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4085856</comments>
            <pubDate>Fri, 15 Oct 2010 21:03:42 +0100</pubDate>
            <guid isPermaLink="false">4085856</guid>        </item>
        <item>
            <title>Characterisation of the epitope for a herpes simplex virus glycoprotein B-specific monoclonal antibody with high protective capacity</title>
            <link>http://www.medworm.com/index.php?rid=4053169&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2t7787mj83020465%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Monoclonal antibody (MAb) 2c, specific for glycoprotein B of herpes simplex virus (HSV), had been shown to mediate clearance
 of infection from the mucous membranes of mice, thereby completely inhibiting mucocutaneous inflammation and lethality, even
 in mice depleted of both CD4+ and CD8+ cells. Additionally, ganglionic infection was highly restricted. In vitro, MAb 2c exhibits a potent complement-independent
 neutralising activity against HSV type 1 and 2, completely inhibits the viral cell-to-cell spread as well as the syncytium
 formation induced by syncytial HSV strains (Eis-Hübinger et al. in Intervirology 32:351–360, 1991; Eis-Hübinger et al. in
 J Gen Virol 74:379–385, 1993). Here, we describe the mapping of the epitope for MAb 2c. The antibody was found t...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4053169</comments>
            <pubDate>Thu, 07 Oct 2010 16:49:19 +0100</pubDate>
            <guid isPermaLink="false">4053169</guid>        </item>
        <item>
            <title>Comparison of pro-inflammatory cytokine expression and cellular signal transduction in human macrophages infected with different influenza A viruses</title>
            <link>http://www.medworm.com/index.php?rid=4001473&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F306067050326lx1v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Influenza A virus infection of macrophages and virus-induced pro-inflammatory gene expression are regarded to contribute to
 severity of influenza A virus-caused diseases. Although some data are available on cytokine production by influenza A virus-infected
 macrophages, systematic comparisons of the virus types are currently considered to be of high relevance in humans (pandemic
 H1N1/2009, seasonal H1N1, seasonal H3N2, highly pathogenic avian influenza H5N1) on pro-inflammatory potential, and relevant
 underlying cellular signalling events are missing. Here, we show that the infection of human monocyte-derived macrophages
 with pandemic H1N1/2009 (A/HH/01/2009), seasonal H1N1/1999 (A/New Caledonia/20/99), seasonal H3N2/2004 (A/California/7/2004)
 or highly pathogenic ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4001473</comments>
            <pubDate>Thu, 23 Sep 2010 17:18:55 +0100</pubDate>
            <guid isPermaLink="false">4001473</guid>        </item>
        <item>
            <title>Multicenter evaluation of a fully automated third-generation anti-HCV antibody screening test with excellent sensitivity and specificity</title>
            <link>http://www.medworm.com/index.php?rid=4001472&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb4234jg172260371%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Early detection of hepatitis C virus (HCV) is an important step in preventing progression to cirrhosis and hepatocellular
 carcinoma. Serologic assays for anti-hepatitis C (anti-HCV) antibody are valuable first-line tests in the screening and diagnosis
 of HCV infection. The aim of this multicenter study was to compare the Elecsys® Anti-HCV assay with alternative CE-marked Anti-HCV antibody assays against a range of samples that included 1,138 blood donors,
 3,553 unselected routine daily specimens, and 46 pre-selected seroconversion panels. Specificity of the Elecsys Anti-HCV assay
 was 99.5% with blood donor samples and 99.4% with routine clinical specimens. These were similar to those obtained with the
 Prism® Anti-HCV, Architect® Anti-HCV assay, ADVIA® Centaur A...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4001472</comments>
            <pubDate>Thu, 23 Sep 2010 17:18:55 +0100</pubDate>
            <guid isPermaLink="false">4001472</guid>        </item>
        <item>
            <title>Prevalence and characteristics of hepatitis B and C virus infections in treatment-naïve HIV-infected patients</title>
            <link>http://www.medworm.com/index.php?rid=3993030&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu1763l838q647291%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In HIV-infected treatment-naïve patients, we analyzed risk factors for either chronic hepatitis B (HBV) infection, occult
 HBV infection (OHBV) or a positive hepatitis C (HCV) serostatus. A total of 918 patients of the RESINA-cohort in Germany were
 included in this study. Before initiating antiretroviral therapy, clinical parameters were collected and blood samples were
 analyzed for antibodies against HIV, HBV and HCV, HBs antigen and viral nucleic acids for HIV and HBV. Present or past HBV
 infection (i.e. HBsAg and/or anti-HBc) was found in 43.4% of patients. HBsAg was detected in 4.5% (41/918) and HBV DNA in
 6.1% (34/554), resulting in OHBV infection in 2.9% (16/554) of patients. OHBV infection could not be ruled out by the presence
 of anti-HBs (50.1%) or the ab...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3993030</comments>
            <pubDate>Sat, 18 Sep 2010 16:54:42 +0100</pubDate>
            <guid isPermaLink="false">3993030</guid>        </item>
        <item>
            <title>Monoassociation with probiotic Lactobacillus delbrueckii UFV-H2b20 stimulates the immune system and protects germfree mice against Listeria monocytogenes infection</title>
            <link>http://www.medworm.com/index.php?rid=3980353&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa463t79142442126%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the present study, we investigated the protective effects of Lactobacillus delbrueckii UFV-H2b20 on the resistance to Listeria monocytogenes infection in gnotobiotic mice. Germfree mice or monoassociated mice were infected with L. monocytogenes, and the microbiological and immunological responses were evaluated after 1, 3, and 5&amp;nbsp;days of infection. Monoassociation
 with L. delbrueckii was capable of protecting mice against death caused by L. monocytogenes and induced a faster clearance of the bacteria in the liver, spleen, and peritoneal cavity at days 1, 3, and 5 post-infection.
 Also, monoassociated mice displayed less liver injury than germfree mice. The production of TNF-α in the serum, peritoneal
 cavity, and gut was augmented in monoassociated mice. Likewi...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3980353</comments>
            <pubDate>Tue, 14 Sep 2010 05:57:19 +0100</pubDate>
            <guid isPermaLink="false">3980353</guid>        </item>
        <item>
            <title>Effect of inhibitors of arachidonic acid metabolism on prostaglandin E2 production by Candida albicans and Candida dubliniensis biofilms</title>
            <link>http://www.medworm.com/index.php?rid=3953519&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F033410681ml6350w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Arachidonic acid (AA) is released from infected host cells during Candida albicans infection and may serve as carbon source for yeast growth and as precursor for the production of biologically active eicosanoids,
 such as prostaglandin E2 (PGE2) by C. albicans. However, the mechanism involved in this production is still unclear. Therefore, it was of interest to investigate the effect
 of different arachidonic acid metabolism inhibitors on PGE2 production by biofilms of C. albicans and the closely related C. dubliniensis. This was done by growing Candida biofilms in the presence of AA as well as cytochrome P450 (CYP), multicopper oxidase, cyclooxygenase or lipoxygenase inhibitors.
 The concentration of PGE2 was determined by a monoclonal PGE2 enzyme-linked immunosorbent ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3953519</comments>
            <pubDate>Wed, 08 Sep 2010 05:16:40 +0100</pubDate>
            <guid isPermaLink="false">3953519</guid>        </item>
        <item>
            <title>PI3K-dependent host cell actin rearrangements are required for Cronobacter sakazakii invasion of human brain microvascular endothelial cells</title>
            <link>http://www.medworm.com/index.php?rid=3932868&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn4q47v183737t603%2F</link>
            <description>In this study, we found that C. sakazakii invasion of human brain microvascular endothelial cells (HBMEC) was significantly inhibited by cytochalasin D, a disrupting
 agent of actin microfilaments. Disassembly of actin stress fibers and cortical actin fibers was observed in HBMEC infected
 with C. sakazakii. C. sakazakii infection leads to increased Akt phosphorylation in HBMEC, which was blocked by treatment with PI3K inhibitors. Meanwhile,
 PI3K and Akt inhibitors significantly inhibited C. sakazakii invasion of HBMEC. Our further results illustrated that the C. sakazakii-induced Akt activation and C. sakazakii invasion were attenuated in HBMEC transfected with dominant-negative PI3K (Δp110). More importantly, the actin filaments
 rearrangements in HBMEC induced by C. sakazakii were eff...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3932868</comments>
            <pubDate>Thu, 02 Sep 2010 06:27:11 +0100</pubDate>
            <guid isPermaLink="false">3932868</guid>        </item>
        <item>
            <title>Seroprevalence of human T-cell lymphotropic virus type 1 and 2 in blood donors from the regional hospital of Valdivia, Chile</title>
            <link>http://www.medworm.com/index.php?rid=3866774&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7415jr4lj3352932%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It is estimated that 15–20&amp;nbsp;millions of people are infected with human T-cell lymphotropic virus 1/2 (HTLV-1/2) worldwide,
 and 20–30% of them are Latin Americans. The seroprevalence rates vary according to geographic area, socio-demographic composition
 and individual risk behaviors. The impact of HTLV-1-associated diseases on the community, as well as the increasing concerns
 about blood transfusion safety due to infectious transmitted agents, has required mandatory screening assays of blood donors
 as an effective preventive strategy in HTLV-1 transmission. The aim of this study was to estimate the seroprevalence of HTLV-1/2
 in blood donors from Valdivia, southern Chile during the first year of mandatory screening of HTLV by Chilean government.
 Blood sample...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3866774</comments>
            <pubDate>Fri, 13 Aug 2010 07:04:29 +0100</pubDate>
            <guid isPermaLink="false">3866774</guid>        </item>
        <item>
            <title>Human immunodeficiency virus type-1 group M quasispecies evolution: diversity and divergence in patients co-infected with active tuberculosis</title>
            <link>http://www.medworm.com/index.php?rid=3866775&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8l80ht62m44nq278%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The evolution of intra-host human immunodeficiency virus type 1 (HIV-1) quasispecies prior and after treating active tuberculosis
 (TB) with chemotherapy in HIV-1/TB patients was assessed. Two time points HIV-1 quasispecies were evaluated by comparing HIV-1-infected
 patients with active tuberculosis (HIV-1/TB) and HIV-1-infected patients without tuberculosis (HIV-1/non-TB). Plasma samples
 were obtained from the Frankfurt HIV cohort, and HIV-1 RNA was isolated. C2V5
 env was amplified by PCR and molecular cloning was performed. Eight to twenty-five clones were sequenced from each patient. Various
 phylogenetic analyses were performed. We found a significant increase in diversity and divergence in HIV-1/TB compared to
 the HIV-1/non-TB. For HIV-1/TB, the average rate of...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3866775</comments>
            <pubDate>Tue, 10 Aug 2010 19:16:48 +0100</pubDate>
            <guid isPermaLink="false">3866775</guid>        </item>
        <item>
            <title>Epstein-Barr virus-associated pneumonia and bronchiolitis obliterans syndrome in a lung transplant recipient</title>
            <link>http://www.medworm.com/index.php?rid=3780091&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F67081908p551l362%2F</link>
            <description>We report the case of a 25-year-old lung and liver transplant recipient who developed respiratory failure. High levels of
 Epstein-Barr virus (EBV) genome copies were detectable in respiratory tract specimens, while the search for various other
 viral, bacterial or fungal pathogens remained empty. Post-transplant lymphoproliferative disease was excluded. Due to the
 rapid progression of respiratory insufficiency, a re-transplantation of the lung was performed. EBV-encoded small RNAs could
 be demonstrated by in situ hybridization within pneumocytes and lymphocytes of the explanted lung tissue. The clinical situation
 improved soon after re-transplantation, and the EBV load detected in the lower respiratory tract decreased significantly.
 
 
	Content Type Journal ArticleCategory Original In...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3780091</comments>
            <pubDate>Tue, 20 Jul 2010 07:53:01 +0100</pubDate>
            <guid isPermaLink="false">3780091</guid>        </item>
        <item>
            <title>Rapid quantitation of cytomegalovirus DNA in whole blood by a new molecular assay based on automated sample preparation and real-time PCR</title>
            <link>http://www.medworm.com/index.php?rid=3678443&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6x114m23827g57r1%2F</link>
            <description>In this study, the analytical performance of the artus™ CMV RG PCR kit in conjunction with automated sample preparation on the new QIAsymphony™ SP instrument was evaluated. Clinically
 referred samples were tested and results compared to those obtained with the routinely used molecular test system. Accuracy
 testing showed results to be within ±0.2 log10 unit of the expected panel results. The assay was linear (R&amp;nbsp;=&amp;nbsp;0.9972) from a lower quantification limit of 148 copies/ml to 1.3&amp;nbsp;×&amp;nbsp;107 copies/ml. The between-day imprecision CV was 8–63%, and the within-run imprecision CV was 16–61%. When 100 clinically referred
 samples were tested, results obtained with the new test system showed an acceptable concordance with those obtained with the
 routinely used easyMAG...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3678443</comments>
            <pubDate>Fri, 18 Jun 2010 10:45:18 +0100</pubDate>
            <guid isPermaLink="false">3678443</guid>        </item>
        <item>
            <title>Hidden hazards of HCV transmission</title>
            <link>http://www.medworm.com/index.php?rid=3563561&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F51616848hl14r2w2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hepatitis C virus infection is a global health problem that has important epidemiological and clinical consequences. It has
 been well established that exposure to infected blood is the main risk factor for HCV transmission. However, in 20% of cases
 the agent transmission occurs by unknown route or in the presence of an unidentified source of infection. Understanding of
 the epidemiology of HCV is needed to help us define future control and preventive strategies. Herein, we discuss about diagnosis
 of HCV infection and hepatitis C surveillance in the context of its transmission.
 
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-010-0159-9Authors
		Robério Amorim de Almeida Pondé, Universidade Federal de Goiás Laboratório de Virologia Humana, Instit...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3563561</comments>
            <pubDate>Wed, 12 May 2010 07:42:12 +0100</pubDate>
            <guid isPermaLink="false">3563561</guid>        </item>
        <item>
            <title>The underlying mechanisms for the “isolated positivity for the hepatitis B surface antigen (HBsAg)” serological profile</title>
            <link>http://www.medworm.com/index.php?rid=3563562&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6187546p023u6608%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During HBV infection, four structural antigen/antibody systems are observed: hepatitis B surface antigen (HBsAg) and its antibody
 (anti-HBs); the pre-S antigens associated with HBsAg particles and their antibodies; the particulate nucleocapsid antigen
 (HBcAg) and anti-HBc; and an antigen structurally related to HBcAg, namely HBeAg and its antibody (anti-HBe). Through the
 examination of this antigen–antibodies system, hepatitis B infection is diagnosed and the course of the disorder may be observed.
 Isolated HBsAg seropositivity is a peculiar serological pattern in HBV infection observed some times in routine laboratory.
 In most cases is not clear how this profile should be interpreted neither its significance. This pattern, however, may be
 associated with some c...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3563562</comments>
            <pubDate>Tue, 11 May 2010 08:25:55 +0100</pubDate>
            <guid isPermaLink="false">3563562</guid>        </item>
        <item>
            <title>Pro-autophagic signal induction by bacterial pore-forming toxins</title>
            <link>http://www.medworm.com/index.php?rid=3555714&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl84h3x26176r1877%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pore-forming toxins (PFT) comprise a large, structurally heterogeneous group of bacterial protein toxins. Nucleated target
 cells mount complex responses which allow them to survive moderate membrane damage by PFT. Autophagy has recently been implicated
 in responses to various PFT, but how this process is triggered is not known, and the significance of the phenomenon is not
 understood. Here, we show that S. aureus α-toxin, Vibrio cholerae cytolysin, streptolysin O and E. coli haemolysin activate two pathways leading to autophagy. The first pathway is triggered via AMP-activated protein kinase (AMPK).
 AMPK is a major energy sensor which induces autophagy by inhibiting the target of rapamycin complex 1 (TORC1) in response
 to a drop of the cellular ATP/AMP-ratio, as i...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3555714</comments>
            <pubDate>Sat, 08 May 2010 10:11:03 +0100</pubDate>
            <guid isPermaLink="false">3555714</guid>        </item>
        <item>
            <title>Chlamydia pneumoniae infection and Alzheimer’s disease: a connection to remember?</title>
            <link>http://www.medworm.com/index.php?rid=3545267&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flq5433213510rq26%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Alzheimer’s disease (AD) is the most common cause of dementia in the elderly, whereby it is customary to distinguish between
 early familial FAD and late-onset AD (LOAD). The development of LOAD, the most prevalent form of AD, is believed to be a multifactorial
 process that may also involve infections with bacterial or viral pathogens. After the first report on the presence of Chlamydia pneumoniae (Cpn) in brains of patients with AD appeared in 1998, this bacterium has most often been implicated in AD pathogenesis. However,
 while some studies demonstrate a clear association between Cpn infection and AD, others have failed to confirm these findings. This might be due to heterogeneity of the specimens analyzed
 and lack of standardized detection methods. Additionally,...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3545267</comments>
            <pubDate>Thu, 06 May 2010 09:00:26 +0100</pubDate>
            <guid isPermaLink="false">3545267</guid>        </item>
        <item>
            <title>Molecular biology of foamy viruses</title>
            <link>http://www.medworm.com/index.php?rid=3545268&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu135454633866776%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;One of the most fascinating areas in retrovirology is the study of foamy viruses (FVs), because these viruses appear to do
 everything that is common to all other retroviruses differently. FVs have found a completely new way to propagate their genome.
 And they do this extremely successfully because most of wild non-human primates, felines, bovines, equines, and small ruminants
 are likely to be non-pathogenically infected. The success of FVs can also be viewed from a different angle, since they replicate
 very conservatively and do not need to shape their genotypic and phenotypic makeup every now and then. The elucidation of
 the underlying basic mechanisms of the FV replication strategy is the topic of this review.
 
 
	Content Type Journal ArticleCategory ReviewDOI 1...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3545268</comments>
            <pubDate>Thu, 06 May 2010 09:00:25 +0100</pubDate>
            <guid isPermaLink="false">3545268</guid>        </item>
        <item>
            <title>Genome dynamics and its impact on evolution of Escherichia coli</title>
            <link>http://www.medworm.com/index.php?rid=3545269&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkg557118l3w6077t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Escherichia coli genome consists of a conserved part, the so-called core genome, which encodes essential cellular functions and of a flexible,
 strain-specific part. Genes that belong to the flexible genome code for factors involved in bacterial fitness and adaptation
 to different environments. Adaptation includes increase in fitness and colonization capacity. Pathogenic as well as non-pathogenic
 bacteria carry mobile and accessory genetic elements such as plasmids, bacteriophages, genomic islands and others, which code
 for functions required for proper adaptation. Escherichia coli is a very good example to study the interdependency of genome architecture and lifestyle of bacteria. Thus, these species
 include pathogenic variants as well as commensal bacteria ada...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3545269</comments>
            <pubDate>Thu, 06 May 2010 09:00:24 +0100</pubDate>
            <guid isPermaLink="false">3545269</guid>        </item>
        <item>
            <title>Family members stick together: multi-protein complexes of malaria parasites</title>
            <link>http://www.medworm.com/index.php?rid=3511193&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F38xm76026k0m048l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malaria parasites express a broad repertoire of proteins whose expression is tightly regulated depending on the life-cycle
 stage of the parasite and the environment of target organs in the respective host. Transmission of malaria parasites from
 the human to the anopheline mosquito is mediated by intraerythrocytic sexual stages, termed gametocytes, which circulate in
 the peripheral blood and are essential for the spread of the tropical disease. In Plasmodium falciparum, gametocytes express numerous extracellular proteins with adhesive motifs, which might mediate important interactions during
 transmission. Among these is a family of six secreted proteins with adhesive modules, termed PfCCp proteins, which are highly conserved throughout the apicomplexan clade. In P. f...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3511193</comments>
            <pubDate>Sat, 24 Apr 2010 08:05:53 +0100</pubDate>
            <guid isPermaLink="false">3511193</guid>        </item>
        <item>
            <title>Resemblance and divergence: the “new” members of the genus Bordetella</title>
            <link>http://www.medworm.com/index.php?rid=3479477&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F242j8483q05r7324%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Bordetella pertussis, the etiological agent of whooping cough, belongs to the bacterial pathogens first described in the so-called golden era
 of microbiology more than 100&amp;nbsp;years ago. In the course of the following decades, several other closely related pathogens were
 described which are nowadays classified in the genus Bordetella together with B. pertussis. These are the human and animal pathogens B. parapertussis, B. bronchiseptica and B. avium which are of high medical or veterinary interest, and which, together with B. pertussis, are referred to as the “classical” Bordetella species. Only in the past 15&amp;nbsp;years, several additional species were classified in the genus, frequently isolated from patients
 with underlying disease, animals or from the envi...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3479477</comments>
            <pubDate>Tue, 13 Apr 2010 18:14:57 +0100</pubDate>
            <guid isPermaLink="false">3479477</guid>        </item>
        <item>
            <title>CD28 and IL-4: two heavyweights controlling the balance between immunity and inflammation</title>
            <link>http://www.medworm.com/index.php?rid=3479476&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2w513318304405q7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The costimulatory receptor CD28 and IL-4Rα-containing cytokine receptors play key roles in controlling the size and quality
 of pathogen-specific immune responses. Thus, CD28-mediated costimulation is needed for effective primary T-cell expansion
 and for the generation and activation of regulatory T-cells (Treg cells), which protect from immunopathology. Similarly, IL-4Rα
 signals are required for alternative activation of macrophages, which counteract inflammation by type 1 responses. Furthermore,
 immune modulation by CD28 and IL-4 is interconnected through the promotion of IL-4 producing T-helper 2 cells by CD28 signals.
 Using conditionally IL-4Rα and CD28 deleting mice, as well as monoclonal antibodies, which block or stimulate CD28, or mAb
 that deplete Treg c...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3479476</comments>
            <pubDate>Tue, 13 Apr 2010 18:14:57 +0100</pubDate>
            <guid isPermaLink="false">3479476</guid>        </item>
        <item>
            <title>Measles virus infection of the CNS: human disease, animal models, and approaches to therapy</title>
            <link>http://www.medworm.com/index.php?rid=3479478&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh0w5131712283005%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Viral infections of the central nervous system (CNS) mostly represent clinically important, often life-threatening complications
 of systemic viral infections. After acute measles, CNS complications may occur early (acute postinfectious measles encephalitis,
 APME) or after years of viral persistence (subacute sclerosing panencephalitis, SSPE). In spite of a presumably functional
 cell-mediated immunity and high antiviral antibody titers, an immunological control of the CNS infection is not achieved in
 patients suffering from SSPE. There is still no specific therapy for acute complications and persistent MV infections of the
 CNS. Hamsters, rats, and (genetically unmodified and modified) mice have been used as model systems to study mechanisms of
 MV-induced CNS infect...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3479478</comments>
            <pubDate>Tue, 13 Apr 2010 18:14:56 +0100</pubDate>
            <guid isPermaLink="false">3479478</guid>        </item>
        <item>
            <title>Regulation of white-opaque switching in Candida albicans</title>
            <link>http://www.medworm.com/index.php?rid=3479479&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1875137p10638733%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The yeast Candida albicans is part of the microflora in most healthy people, but can become a pathogen when host defenses are compromised. The phenotypic
 plasticity of C. albicans, which includes switching between different morphologies, contributes to its ability to colonize and infect virtually all
 body locations. A particularly fascinating developmental program is white-opaque switching, a reversible transition between
 the normal yeast morphology (white) and an elongated cell type (opaque), which is the mating-competent form of this fungus.
 Although opaque cells are much less able than white cells to cause a systemic infection, they are better adapted for colonization
 of specific host niches, like skin. White-opaque switching is controlled by the mating type loc...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3479479</comments>
            <pubDate>Tue, 13 Apr 2010 18:14:54 +0100</pubDate>
            <guid isPermaLink="false">3479479</guid>        </item>
        <item>
            <title>Glycyrrhizin inhibits highly pathogenic H5N1 influenza A virus-induced pro-inflammatory cytokine and chemokine expression in human macrophages</title>
            <link>http://www.medworm.com/index.php?rid=3467342&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq787734m82052720%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hypercytokinaemia is thought to contribute to highly pathogenic H5N1 influenza A virus disease. Glycyrrhizin is known to exert
 immunomodulatory and anti-inflammatory effects and therefore a candidate drug for the control of H5N1-induced pro-inflammatory
 gene expression. Here, the effects of an approved parenteral glycyrrhizin preparation were investigated on H5N1 virus replication,
 H5N1-induced pro-inflammatory responses, and H5N1-induced apoptosis in human monocyte-derived macrophages. Glycyrrhizin 100&amp;nbsp;μg/ml,
 a therapeutically achievable concentration, impaired H5N1-induced production of CXCL10, interleukin 6, and CCL5 and inhibited
 H5N1-induced apoptosis but did not interfere with H5N1 replication. Global inhibition of immune responses may result in the
 lo...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3467342</comments>
            <pubDate>Mon, 12 Apr 2010 17:47:00 +0100</pubDate>
            <guid isPermaLink="false">3467342</guid>        </item>
        <item>
            <title>Virulence determinants involved in differential host niche adaptation of Neisseriameningitidis and Neisseria gonorrhoeae</title>
            <link>http://www.medworm.com/index.php?rid=3467343&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv73h165328168594%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Neisseria meningitidis and Neisseria gonorrhoeae are the only pathogenic species of the genus Neisseria. Although these two species are closely related, they specialized on survival in completely different environments within
 the human host—the nasopharynx in the case of N. meningitidis versus the urogenital tract in the case of N. gonorrhoeae. The genetic background of these differences has not yet been determined. Here, we present a comparison of all characterized
 transcriptional regulators in these species, delineating analogous functions and disclosing differential functional developments
 of these DNA-binding proteins with a special focus on the recently characterized regulator FarR and its contribution to divergent
 host niche adaptation in the two Neisseria...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3467343</comments>
            <pubDate>Thu, 08 Apr 2010 18:00:40 +0100</pubDate>
            <guid isPermaLink="false">3467343</guid>        </item>
        <item>
            <title>Subsets, expansion and activation of myeloid-derived suppressor cells</title>
            <link>http://www.medworm.com/index.php?rid=3453351&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh32138704j864041%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tumor cells and microorganisms manipulate the immune system to minimize any counter response in order to survive. Myeloid-derived
 suppressor cells (MDSC) in the mouse represent activated Gr-1+ CD11b+ myeloid precursor cells. Activation may occur through endogenous or exogenous factors leading to the suppression of immune
 responses. Under steady state conditions the same precursors differentiate into dendritic cells, macrophages and neutrophils.
 Their linkage to tumor progression and several suppression mechanisms employing the arginine metabolism are well documented,
 but knowledge of their role in chronic infections, autoimmune diseases and graft-versus-host reactions is just emerging. Several
 factors have been described to promote MDSC expansion and activation in ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3453351</comments>
            <pubDate>Wed, 07 Apr 2010 19:18:49 +0100</pubDate>
            <guid isPermaLink="false">3453351</guid>        </item>
        <item>
            <title>Measles virus-induced immunosuppression: from effectors to mechanisms</title>
            <link>http://www.medworm.com/index.php?rid=3453350&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh3mn68t953505vq3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Immunosuppression is the major cause of infant death associated with acute measles. Hallmarks of this generalized modulation
 of immune functions include: (1) lymphopenia, (2) a prolonged cytokine imbalance consistent with suppression of cellular immunity
 to secondary infections and (3) silencing of peripheral blood lymphocytes that fail to expand in response to ex vivo stimulation. Lymphopenia results from depletion of T cells by mechanisms also involving MV infection, and expression of the
 major MV receptor CD150 plays an important role for targeting these cells. Virus transfer to T cells is thought to be mediated
 by dendritic cells (DCs), which are considered as central to the induction of T-cell silencing and functional skewing. MV
 interaction modulates function...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3453350</comments>
            <pubDate>Wed, 07 Apr 2010 19:18:49 +0100</pubDate>
            <guid isPermaLink="false">3453350</guid>        </item>
        <item>
            <title>Biofilm formation by the human pathogen Neisseria meningitidis</title>
            <link>http://www.medworm.com/index.php?rid=3467344&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqj177x588210786w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The past decade has seen an increasing interest in biofilm formation by Neisseria meningitidis, a human facultative pathogen causing life-threatening childhood disease commencing from asymptomatic nasopharyngeal colonization.
 Studying the biology of in vitro biofilm formation improves the understanding of inter-bacterial processes in asymptomatic
 carriage, of bacterial aggregate formation on host cells, and of meningococcal population biology. This paper reviews publications
 referring to meningococcal biofilm formation with an emphasis on the role of motility and of extracellular DNA. The theory
 of sub-dividing the meningococcal population in settler and spreader lineages is discussed, which provides a mechanistic framework
 for the assumed balance of colonization e...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3467344</comments>
            <pubDate>Wed, 07 Apr 2010 19:18:48 +0100</pubDate>
            <guid isPermaLink="false">3467344</guid>        </item>
        <item>
            <title>The role of evolutionarily conserved signalling systems in Echinococcus multilocularis development and host–parasite interaction</title>
            <link>http://www.medworm.com/index.php?rid=3453352&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgu10117090275568%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Alveolar echinococcosis, one of the most serious and life-threatening zoonoses in the world, is caused by the metacestode
 larval stage of the fox-tapeworm Echinococcus multilocularis. Mostly due to its accessibility to in vitro cultivation, this parasite has recently evolved into an experimental model system
 to study larval cestode development and associated host–parasite interaction mechanisms. Respective advances include the establishment
 of axenic in vitro cultivation systems for parasite larvae as well as culture systems by which the early development of metacestode
 vesicles from totipotent parasite stem cells can be reconstituted under controlled laboratory conditions. A series of evolutionarily
 conserved signalling molecules of the insulin, epidermal growth...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3453352</comments>
            <pubDate>Wed, 07 Apr 2010 19:18:47 +0100</pubDate>
            <guid isPermaLink="false">3453352</guid>        </item>
        <item>
            <title>The CFP-10/ESAT-6 complex of Mycobacterium tuberculosis potentiates the activation of murine macrophages involvement of IFN-γ signaling</title>
            <link>http://www.medworm.com/index.php?rid=3373833&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyu2111n301ntttw4%2F</link>
            <description>In this study, we investigated the influence of
 the CFP-10/ESAT-6 complex on production of IL-12 and nitric oxide (NO) produced by the ANA-1 macrophage cell line. Preincubation
 with the complex in a time-dependent manner significantly enhanced production of NO and IL-12 released from ANA-1 cells following
 IFN-γ stimulation. In addition, the complex up-modulated expression level of IFN-γR1 on surface of the macrophages. Furthermore,
 the effect of the complex on production of IL-12 and NO in ANA-1 cells was suppressed by AG490, a selective inhibitor of JAK/STAT
 pathway. These data suggest that in the presence of IFN-γ, CFP-10/ESAT-6 complex represents a new immunogenicity and protective
 factor that may be, at least partly, due to up modulation of IFN-γR1 expression and activation o...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3373833</comments>
            <pubDate>Mon, 15 Mar 2010 17:55:01 +0100</pubDate>
            <guid isPermaLink="false">3373833</guid>        </item>
        <item>
            <title>Regional spread of HIV-1 M subtype B in middle-aged patients by random env-C2V4 region sequencing</title>
            <link>http://www.medworm.com/index.php?rid=3362236&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F952475lp4w30321n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A transmission cluster of HIV-1 M:B was identified in 11 patients with a median age of 52 (range 26–65) in North-East Germany
 by C2V4 region sequencing of the env gene of HIV-1, who—except of one—were not aware of any risky behaviour. The 10 male and 1 female patients deteriorated immunologically,
 according to their information made available, within 4&amp;nbsp;years after a putative HIV acquisition. Nucleic acid sequence analysis
 showed a R5 virus in all patients and in 7 of 11 a crown motif of the V3 loop, GPGSALFTT, which is found rarely. Analysis
 of formation of this cluster showed that there is still a huge discrepancy between awareness and behaviour regarding HIV transmission
 in middle-aged patients, and that a local outbreak can be detected by nucleic acid...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3362236</comments>
            <pubDate>Wed, 10 Mar 2010 18:29:50 +0100</pubDate>
            <guid isPermaLink="false">3362236</guid>        </item>
        <item>
            <title>Determination of serum antibodies against swine-origin influenza A virus H1N1/09 by immunofluorescence, haemagglutination inhibition, and by neutralization tests: how is the prevalence rate of protecting antibodies in humans?</title>
            <link>http://www.medworm.com/index.php?rid=3283251&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw460vu379406411r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In April 2009, a new variant of influenza A virus, subtype H1N1v emerged in Mexico and spread all over the world producing
 the H1N1 pandemic in mankind after 1918–1920 and 1978/1979. Obviously there was no herd immunity against this new virus variant.
 Mainly young people, but less elderly were affected and presented severe and even lethal courses of disease. Since virus-specific
 antibodies are commonly regarded as markers of partial or complete immunoprotection, we performed antibody determinations
 in serum samples obtained from people before and after the pandemic has arrived in our region (Frankfurt/M., Germany). The
 assays were done by indirect immunofluorescence, by neutralization test, and by a haemagglutination inhibition test (HI),
 which was established i...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3283251</comments>
            <pubDate>Tue, 16 Feb 2010 18:06:20 +0100</pubDate>
            <guid isPermaLink="false">3283251</guid>        </item>
        <item>
            <title>Lymphocyte transformation test detects a response to Campylobacter jejuni antigens in patients with Guillain-Barré syndrome</title>
            <link>http://www.medworm.com/index.php?rid=3279658&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy78j6513332n1510%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Guillain-Barré syndrome (GBS) is an immune-mediated polyneuropathy. Campylobacter jejuni-associated gastrointestinal infection is identified as a major precipitating agent of GBS; however, a standard test to diagnose
 this infection in patients with GBS is lacking. The aim of the present study was to evaluate an outer membrane protein (OMP)-based
 lymphocyte transformation test (LTT) for the diagnosis of C. jejuni infection in GBS. Forty patients with GBS, age and gender matched 52 healthy controls (HC) and 46 disease controls (DC) were
 analyzed for C. jejuni infection by culture, polymerase chain reaction (PCR) and LTT. Lymphocytes at concentration of 1&amp;nbsp;×&amp;nbsp;106/well isolated from GBS patients and controls were stimulated with 20&amp;nbsp;μg/ml of C. jejuni OMP,...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3279658</comments>
            <pubDate>Mon, 15 Feb 2010 17:59:45 +0100</pubDate>
            <guid isPermaLink="false">3279658</guid>        </item>
        <item>
            <title>Mucosal innate response stimulation induced by lipopolysaccharide protects against Bordetella pertussis colonization</title>
            <link>http://www.medworm.com/index.php?rid=3266633&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2r430h65858561n1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Non-specific enhancement of the airways innate response has been shown to impair lung infections in several models of infection
 such diverse as influenza A, Streptococcus pneumoniae, and Aspergillus niger. Our aim was to evaluate whether a similar event could operate in the context of Bordetella pertussis respiratory infection, not only to enrich the knowledge of host–bacteria interaction but also to establish immunological
 basis for the development of new control strategies against the pathogen. Using a B. pertussis intranasal infection model and coadministration of different TLR agonists at the moment of the infection, we observed that
 the enhancement of innate response activation, in a TLR4-dependent way, could efficiently impair B. pertussis colonization (P&amp;nbs...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3266633</comments>
            <pubDate>Mon, 08 Feb 2010 17:29:07 +0100</pubDate>
            <guid isPermaLink="false">3266633</guid>        </item>
        <item>
            <title>Presence of Borrelia burgdorferi in endomyocardial biopsies in patients with new-onset unexplained dilated cardiomyopathy</title>
            <link>http://www.medworm.com/index.php?rid=3156271&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb8x4742136623114%2F</link>
            <description>In conclusion, Bb infection may represent
 an important cause of new-onset unexplained DCM in patients living in endemic regions such as the Czech Republic. Because
 the antibiotic treatment appears to be markedly effective and serological examination does not provide a tool for diagnosing
 the disease, EMB focused on the detection of Bb should be performed in all patients from endemic areas with new-onset unexplained
 DCM not responding to conventional therapy.
 
	Content Type Journal ArticleCategory Rapid CommunicationDOI 10.1007/s00430-009-0141-6Authors
		Tomas Palecek, Charles University of Prague 1st Medical Faculty, 2nd Medical Department - Clinical Department of Cardiology and Angiology Prague Czech RepublicPetr Kuchynka, Charles University of Prague 1st Medical Faculty, 2nd Medical...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3156271</comments>
            <pubDate>Tue, 05 Jan 2010 16:58:32 +0100</pubDate>
            <guid isPermaLink="false">3156271</guid>        </item>
        <item>
            <title>Erratum to: Local and remote tissue injury upon intestinal ischemia and reperfusion depends on the TLR/MyD88 signaling pathway</title>
            <link>http://www.medworm.com/index.php?rid=3118595&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw264k07500247750%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s00430-009-0140-7Authors
		Tatiana Victoni, University of São Paulo Department of Pharmacology, Institute of Biomedical Sciences São Paulo 05508-900 BrazilFernando Rodrigues Coelho, University of São Paulo Department of Pharmacology, Institute of Biomedical Sciences São Paulo 05508-900 BrazilAlexandre Learth Soares, University of São Paulo Department of Pharmacology, Institute of Biomedical Sciences São Paulo 05508-900 BrazilAndressa de Freitas, University of São Paulo Department of Pharmacology, School of Medicine of Ribeirão Preto Ribeirão Preto 14049-900 BrazilThomas Secher, University and CNRS Molecular Immunology and Embryology UMR6218, Cedex 2 45071 Orléans FranceRodrigo Guabiraba, University and CNRS Molecular Immun...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3118595</comments>
            <pubDate>Mon, 21 Dec 2009 23:00:04 +0100</pubDate>
            <guid isPermaLink="false">3118595</guid>        </item>
        <item>
            <title>Tumor cells infected with oncolytic influenza A virus prime natural killer cells for lysis of resistant tumor cells</title>
            <link>http://www.medworm.com/index.php?rid=3100208&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgm356p12p0585r21%2F</link>
            <description>In this study, major histocompatibility complex class
 I (MHC-I)-negative LNCaP and MHC-I-positive DU145 cells were infected with genetically modified influenza A virus lacking
 the non-structural gene 1 (&amp;#8710;NS1 IAV). The cells were used to investigate the influence of &amp;#8710;NS1 IAV infection on NK cell lysis
 of tumor cells as well as to prime NK cells for lysis of LNCaP and DU145 cells. While LNCaP cells infected with ΔNS1 IAV showed
 enhanced lysis when compared with mock-infected cells (93%&amp;nbsp;±&amp;nbsp;1.47 vs. 52%&amp;nbsp;±&amp;nbsp;0.74), both mock-infected and ΔNS1 IAV-infected
 DU145 cells were resistant to NK cell lysis. Moreover, NK cells primed with ΔNS1 IAV-infected LNCaP/DU145 cells effectively
 lysed resistant DU145 and sensitive LNCaP cells to a greater extent than NK cel...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3100208</comments>
            <pubDate>Tue, 15 Dec 2009 06:48:02 +0100</pubDate>
            <guid isPermaLink="false">3100208</guid>        </item>
        <item>
            <title>Induction of immune response to the 17 kDa OMPA Burkholderia cenocepacia polypeptide and protection against pulmonary infection in mice after nasal vaccination with an OMP nanoemulsion-based vaccine</title>
            <link>http://www.medworm.com/index.php?rid=3100209&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F62481r874342k688%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Burkholderia cepacia complex (Bcc) are opportunistic bacteria associated with life-threatening illness in persons with cystic fibrosis. Once Bcc
 colonization is established, these antimicrobial-resistant and biofilm-forming bacteria are difficult to eradicate and are
 associated with increased rates of morbidity and mortality. At present, no vaccines are available to prevent the Bcc infection.
 There is currently a paucity of published information regarding the development of vaccines designed to prevent Burkholderia colonization. This work expands on the recent studies published by Bertot et al. [Infect Immun 75(6):2740–2752, 2007], where
 successful protective immune responses were generated in mice using a B. multivorans OMP-based vaccine. Here, we evaluate an e...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3100209</comments>
            <pubDate>Sun, 06 Dec 2009 00:50:39 +0100</pubDate>
            <guid isPermaLink="false">3100209</guid>        </item>
        <item>
            <title>Induction of immune response to the 17 kDa OMPA Burkholderia cenocepacia polypeptide and protection against pulmonary infection in mice after nasal vaccination with an OMP nanoemulsion-based vaccine</title>
            <link>http://www.medworm.com/index.php?rid=3066648&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F62481r874342k688%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Burkholderia cepacia complex (Bcc) are opportunistic bacteria associated with life-threatening illness in persons with cystic fibrosis. Once Bcc
 colonization is established, these antimicrobial-resistant and biofilm-forming bacteria are difficult to eradicate and are
 associated with increased rates of morbidity and mortality. At present, no vaccines are available to prevent the Bcc infection.
 There is currently a paucity of published information regarding the development of vaccines designed to prevent Burkholderia colonization. This work expands on the recent studies published by Bertot et al. [Infect Immun 75(6):2740–2752, 2007], where
 successful protective immune responses were generated in mice using a B. multivorans OMP-based vaccine. Here, we evaluate an e...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3066648</comments>
            <pubDate>Sun, 06 Dec 2009 00:50:39 +0100</pubDate>
            <guid isPermaLink="false">3066648</guid>        </item>
        <item>
            <title>Prophylactic effect of bacteriophages on mice subjected to chemotherapy-induced immunosuppression and bone marrow transplant upon infection with Staphylococcus aureus</title>
            <link>http://www.medworm.com/index.php?rid=3066649&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F233807269r2h2725%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Due to the increased resistance of bacteria to antibiotics, phage therapy may be an alternative to treat or prevent suppurative
 infections in immunocompromised patients. The authors’ recent studies indicated that such an approach is particularly beneficial
 in immunosuppressed mice. A5/L bacteriophages, specific for the Staphylococcus aureus strain L, were tested for their ability to protect CBA mice subjected to myeloablative (busulfan) and immunosuppressive (cyclophosphamide)
 conditioning followed by a syngeneic bone marrow transplantation (BMT) and infected with a sublethal or lethal dose of bacteria.
 The application of phages to immunocompromised mice given BMT led to a significant (&amp;gt;90%) reduction in bacterial load in the
 spleen and liver. Moreover, 72% of...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3066649</comments>
            <pubDate>Tue, 01 Dec 2009 20:57:27 +0100</pubDate>
            <guid isPermaLink="false">3066649</guid>        </item>
        <item>
            <title>Epidemiology of Human Cytomegalovirus (HCMV) in an urban region of Germany: what has changed?</title>
            <link>http://www.medworm.com/index.php?rid=3056222&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq1057q627v254j14%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since the dynamics of transmission of human cytomegalovirus (HCMV) have not been clarified yet, we assessed a possible change
 in HCMV seroprevalence in Frankfurt am Main, Germany during the past twenty years and tried to detect variables with an impact
 on epidemiology. Between 1/1/1988 and 10/15/2008, a total of 54443 serum samples were collected for routine diagnostics and
 analyzed using Enzygnost Anti HCMV-IgG enzyme immunoassay (Siemens/Dade Behring, Marburg, Germany). Two decades, 1/1/1988–12/31/1997
 and 1/1/1998–10/15/2008, and several groups (type of health insurance, gender, age, HIV-status) were evaluated to assess changes
 in seroprevalence. Regarding both decades, the overall age-adjusted prevalence of HIV-negative patients dropped from 63.70%
 (confid...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3056222</comments>
            <pubDate>Tue, 01 Dec 2009 08:30:06 +0100</pubDate>
            <guid isPermaLink="false">3056222</guid>        </item>
        <item>
            <title>TGF-β and CD23 are involved in nitric oxide production by pulmonary macrophages activated by β-glucan from Paracoccidioides brasiliensis</title>
            <link>http://www.medworm.com/index.php?rid=3056223&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0pp4234694645l36%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pulmonary macrophages (PM), which are CD11b/CD18+ and CD23+, may be involved in the onset of inflammatory events caused by Paracoccidioides brasiliensis in the lungs. In the present study, we measured the nitric oxide (NO) and interleukin in PM production after intratracheal
 (i.t.) inoculation of an enriched β-glucan cell wall fraction from P. brasiliensis (Fraction F1). BALB/c and C57/BL6 (B6) mice were i.t. treated with Fraction F1, and their PM were restimulated in vitro with
 LPS and interferon-γ up to 14&amp;nbsp;days after treatment. Macrophages BALB/c mice produced less NO than PM from B6 mice. The lower
 NO production was caused by higher production of TGF-β by pulmonary macrophages of BALB/c and was abrogated by anti-TGF-β
 MoAb in vitro and in vivo. Other int...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3056223</comments>
            <pubDate>Tue, 01 Dec 2009 08:30:05 +0100</pubDate>
            <guid isPermaLink="false">3056223</guid>        </item>
        <item>
            <title>Local and remote tissue injury upon intestinal ischemia and reperfusion depends on the TLR/MyD88 signaling pathway</title>
            <link>http://www.medworm.com/index.php?rid=3044229&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyx2574x2m72l13wg%2F</link>
            <description>In conclusion, our data demonstrate that disruption of the TLR/MyD88 pathway in mice attenuates acute
 intestinal and lung injury, inflammation, and endothelial damage allowing enhanced survival.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-009-0134-5Authors
		Tatiana Victoni, University of São Paulo Department of Pharmacology, Institute of Biomedical Sciences São Paulo 05508-900 BrazilFernando Rodrigues Coelho, University of São Paulo Department of Pharmacology, Institute of Biomedical Sciences São Paulo 05508-900 BrazilAlexandre Learth Soares, University of São Paulo Department of Pharmacology, Institute of Biomedical Sciences São Paulo 05508-900 BrazilAndressa de Freitas, University of São Paulo Department of Pharmacology, School of Medicine of...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3044229</comments>
            <pubDate>Thu, 26 Nov 2009 07:59:16 +0100</pubDate>
            <guid isPermaLink="false">3044229</guid>        </item>
        <item>
            <title>Hand, foot and mouth disease: seroprevalence of Coxsackie A16 and Enterovirus 71 in Germany</title>
            <link>http://www.medworm.com/index.php?rid=3044230&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff27221l0522119r6%2F</link>
            <description>The objective of the study was to analyze CA16 and EV71 seroepidemiologically in
 the population of Frankfurt/M., Germany. A total of 696 individuals (349 males and 347 females, divided into seven different
 age groups, 1–4, 5–9, 10–14, 15–19, 20–39, 40–59 and &amp;gt;60&amp;nbsp;years) were tested for serum antibodies against CA16 and EV71 by
 the use of a microneutralization test. Sera were collected at the Frankfurt university hospital from patients suffering from
 other diseases between March and September 2006. CA16 and EV71 infections were observed to be widely present in the population.
 The age-adjusted seroprevalence for individuals ≥1&amp;nbsp;year was found to be 62.9% for CA16 and 42.8% for EV71 without a gender-specific
 significant difference. Only 12.0 and 27.0% of the chi...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3044230</comments>
            <pubDate>Thu, 26 Nov 2009 07:59:15 +0100</pubDate>
            <guid isPermaLink="false">3044230</guid>        </item>
        <item>
            <title>Long-term flaxseed oil supplementation diet protects BALB/c mice against Streptococcus pneumoniae infection</title>
            <link>http://www.medworm.com/index.php?rid=3011987&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk4807387t1781814%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intense host immune response to infection contributes significantly to the pathology of pneumococcal pneumonia. Therefore,
 the regulation of host immune response is critical for the successful outcome of pneumonia in such patients. The aim of the
 present study was to investigate the effect of n-3 PUFA, i.e. flaxseed oil supplementation for short (4&amp;nbsp;weeks) as well as
 long (9&amp;nbsp;weeks) term, on the course of S. pneumoniae D39 serotype 2 infection in mice. The efficacy of flaxseed oil supplementation was investigated in terms of survival of animals
 and production of various inflammatory molecules (malondialdehyde, myeloperoxidase, nitric oxide) in the lung homogenate of
 animals. This was correlated with bacteriological and histopathological parameters. The immu...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3011987</comments>
            <pubDate>Tue, 17 Nov 2009 23:51:09 +0100</pubDate>
            <guid isPermaLink="false">3011987</guid>        </item>
        <item>
            <title>Antiviral therapy of chronic hepatitis C in patients with advanced liver disease and after liver transplantation</title>
            <link>http://www.medworm.com/index.php?rid=2984534&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx55482v472462gu1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chronic infection with the hepatitis C virus (HCV) represents one of the major causes for end-stage liver disease worldwide.
 Although liver transplantation offers an effective treatment, HCV reinfection of the transplanted graft is a critical and
 almost inevitable complication with major influence on graft- and patient survival. Pre-transplant antiviral therapy in advanced
 liver disease is limited by poor tolerance and only applicable to mildly decompensated patients but was able to show promising
 results in patients reaching negative viral load when undergoing transplantation. Prophylactic therapy with HCV antibodies
 during the anhepatic phase has not been shown to be effective in studies to date. Antiviral therapy after transplantation
 but before evidence of rei...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2984534</comments>
            <pubDate>Mon, 09 Nov 2009 19:13:57 +0100</pubDate>
            <guid isPermaLink="false">2984534</guid>        </item>
        <item>
            <title>Cellular immune response to Mycobacterium tuberculosis-specific antigen culture filtrate protein-10 in south India</title>
            <link>http://www.medworm.com/index.php?rid=2984535&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnl4381251123357u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The Mycobacterium tuberculosis (M. tuberculosis)-specific culture filtrate protein-10 (CFP-10) is highly recognized by M. tuberculosis infected subjects. In the present study, the proliferative response and IFN-γ secretion was found for C-terminal peptides
 of the protein (Cfp651–70, Cfp761–80, Cfp871–90, and Cfp981–100). The alleles HLA DRB1 *04 and HLA DRB1 *10 recognized the C-terminal peptides Cfp7, Cfp8, and Cfp9 in HHC. Cfp6 was predominantly
 recognized by the alleles HLA DRB1 *03 and HLA DRB1 *15 by PTB. The minimal nonameric epitopes from the C-terminal region
 were CFP-1056–64 and CFP-1076–84. These two peptides deserve attention for inclusion in a vaccine against tuberculosis in this region.
 
	Content Type Journal ArticleCategory Original Invest...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2984535</comments>
            <pubDate>Mon, 09 Nov 2009 19:13:56 +0100</pubDate>
            <guid isPermaLink="false">2984535</guid>        </item>
        <item>
            <title>Possible hidden hazards of mass vaccination against new influenza A/H1N1: have the cardiovascular risks been adequately weighed?</title>
            <link>http://www.medworm.com/index.php?rid=2924726&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26r335851h17584g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Programs for vaccination against the new influenza A/H1N1 targeting many hundred million citizens in Europe and the USA are
 to be launched in the fall of this year. The USA is planning to employ a non-adjuvanted vaccine, whereas European nations
 are opting for inclusion of MF59, the adjuvant contained in an alternative seasonal flu vaccine, or the related adjuvant AS03
 that is contained in a recently developed H5N1 vaccine. We draw attention to unappreciated hazards of using adjuvanted vaccine
 in Europe. Evidence from animal experiments in conjunction with clinical epidemiological data indicates that, quite irrespective
 of cause, stimulation of the immune system may accelerate atherogenesis. Application of adjuvanted flu vaccines to individuals
 at risk may therefo...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2924726</comments>
            <pubDate>Thu, 22 Oct 2009 18:56:22 +0100</pubDate>
            <guid isPermaLink="false">2924726</guid>        </item>
        <item>
            <title>Multicentre evaluation of the Elecsys® hepatitis B surface antigen II assay for detection of HBsAg in comparison with other commercially available assays</title>
            <link>http://www.medworm.com/index.php?rid=2908288&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbn25480m0212327l%2F</link>
            <description>In conclusion, it was demonstrated that the
 Elecsys HBsAg II assay is suitable for routine HBsAg screening in China.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-009-0127-4Authors
		Ji-Dong Jia, Capital Medical University Beijing Friendship Hospital 95 Yong-an Road 100050 Xuanwu District, Beijing People’s Republic of ChinaMa Hong, Capital Medical University Beijing Friendship Hospital 95 Yong-an Road 100050 Xuanwu District, Beijing People’s Republic of ChinaLai Wei, Peking University Hepatology Institute Peking University People’s Hospital Beijing People’s Republic of ChinaXin-Xin Zhang, Shanghai Jiatong University Ruijin Hospital, School of Medicine Shanghai People’s Republic of ChinaYuan-Li Mao, Beijing 302 Military Hospital of China Beijing...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2908288</comments>
            <pubDate>Thu, 15 Oct 2009 17:54:06 +0100</pubDate>
            <guid isPermaLink="false">2908288</guid>        </item>
        <item>
            <title>Survival of the fittest: how Brucella strains adapt to their intracellular niche in the host</title>
            <link>http://www.medworm.com/index.php?rid=2898422&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa2j7818n6797u754%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Brucella strains produce abortion and infertility in their natural hosts and a zoonotic disease in humans known as undulant fever.
 These bacteria do not produce classical virulence factors, and their capacity to successfully survive and replicate within
 a variety of host cells underlies their pathogenicity. Extensive replication of the brucellae in placental trophoblasts is
 associated with reproductive tract pathology in natural hosts, and prolonged persistence in macrophages leads to the chronic
 infections that are a hallmark of brucellosis in both natural hosts and humans. This review describes how Brucella strains have efficiently adapted to their intracellular lifestyle in the host.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-009-0123-8Aut...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2898422</comments>
            <pubDate>Wed, 14 Oct 2009 17:00:14 +0100</pubDate>
            <guid isPermaLink="false">2898422</guid>        </item>
        <item>
            <title>Measurement of cytotoxic T lymphocyte activity of human cytomegalovirus seropositive individuals by a highly sensitive coupled luminescent method</title>
            <link>http://www.medworm.com/index.php?rid=2879265&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl32124740l0418uw%2F</link>
            <description>In conclusion,
 CLM represents a highly sensitive, fast, material-saving and non-toxic/non-radioactive method for the measurement of antigen-specific
 CTL cytotoxic activity.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-009-0126-5Authors
		Henry Ogbomo, Klinikum der Johann Wolfgang Goethe-Universität Institut für Medizinische Virologie, Zentrum der Hygiene Paul-Ehrlich-Str. 40 60596 Frankfurt am Main GermanyJanina Geiler, Klinikum der Johann Wolfgang Goethe-Universität Institut für Medizinische Virologie, Zentrum der Hygiene Paul-Ehrlich-Str. 40 60596 Frankfurt am Main GermanyAnke Leutz, Klinikum der Johann Wolfgang Goethe-Universität Institut für Medizinische Virologie, Zentrum der Hygiene Paul-Ehrlich-Str. 40 60596 Frankfurt am Main GermanyKristi...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2879265</comments>
            <pubDate>Thu, 08 Oct 2009 07:15:41 +0100</pubDate>
            <guid isPermaLink="false">2879265</guid>        </item>
        <item>
            <title>Humoral immune responses and protective efficacy of sequential B- and T-cell epitopes of V antigen of Yersinia pestis by intranasal immunization in microparticles</title>
            <link>http://www.medworm.com/index.php?rid=2842243&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpw0t635821852464%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Capsular F1 and secretory V antigen are the putative vaccine candidates for plague, caused by Yersinia pestis. Contemplating this, we studied the immunogenicity and protective efficacy of collinearly synthesized B- and T-cell epitopes
 (B-T constructs) of V antigen entrapped in poly (dl-lactide-co-glycolide) microparticles immunized intranasally using single dose immunization schedule in outbred, H-2b and H-2d mice. High antibody levels were observed in terms of IgG, IgA and SIgA peak titers in sera and mucosal washes to different
 B-T constructs. The constructs ai, bi and fi especially showed high peak antibody titers ranging from 51,200 to 204,000, which were maintained till day 120 post immunization.
 IgG/IgA Specific activity in sera and washes correlated well with ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2842243</comments>
            <pubDate>Thu, 24 Sep 2009 16:42:06 +0100</pubDate>
            <guid isPermaLink="false">2842243</guid>        </item>
        <item>
            <title>Ross River virus infection in a traveller returning from northern Australia</title>
            <link>http://www.medworm.com/index.php?rid=2768516&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdj055611727675g1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ross River virus is an arthropod-borne alphavirus (family Togaviridae) causing epidemic polyarthritis in the Australia-Pacific region. The infection causes substantial morbidity due to long-lasting
 arthralgia. Despite being the most common arboviral infection in Australia, reports in travellers are scarce. Here, we describe
 the disease in a German traveller who was not aware of the prevalence of this infection in his holiday destination, the Northern
 Territory and Queensland, Australia. The patient had neither fever nor rash, but presented with chills, watery diarrhoea and
 severe, prolonged arthritis.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s00430-009-0122-9Authors
		Dennis Tappe, University of Würzburg Institute of Hygiene and Microbiology J...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2768516</comments>
            <pubDate>Thu, 03 Sep 2009 06:25:57 +0100</pubDate>
            <guid isPermaLink="false">2768516</guid>        </item>
        <item>
            <title>The clinical value of neutrophil extracellular traps</title>
            <link>http://www.medworm.com/index.php?rid=2681589&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F63413j422r240221%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Neutrophil extracellular traps (NETs) have recently been discovered as a central part of antimicrobial innate immunity. In
 the meanwhile, evidence accumulated that NETs are also generated upon non-infectious stimuli in various clinical settings.
 In acute or chronic inflammatory disorders aberrantly enhanced NET formation and/or decreased NET degradation seems to correlate
 with disease outcome. This review summarizes current knowledge about the relation of NETs in a broad spectrum of clinical
 settings. Specifically, we focus on the importance of NETs as a predictive marker in severely ill patients and further, we
 speculate about the potential pathophysiology of NETs.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-009-0121-xAuthors
		Tim Lögters, H...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2681589</comments>
            <pubDate>Mon, 03 Aug 2009 20:44:56 +0100</pubDate>
            <guid isPermaLink="false">2681589</guid>        </item>
        <item>
            <title>Manganese-induced changes of the biochemical characteristics of the recombinant wild-type and mutant PrPs</title>
            <link>http://www.medworm.com/index.php?rid=2644808&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh387882261j76507%2F</link>
            <description>In this study, recombinant human wild-type (WT) PrP and
 PrP mutants with deleted or inserted octarepeats were exposed to manganese, and their biochemical and biophysical characteristics
 were evaluated by proteinase K (PK) digestion, sedimentation experiments, transmission electron microscopy and circular dichroism.
 It demonstrated that incubation of manganese remarkably increased PK-resistances, protein aggregations and β-sheet contents
 of the PrPs. Moreover, the PrP mutants of inserted or deleted octarepeats were much vulnerable to the influence of manganese,
 which showed obviously more aggregation and higher β-sheet content than that of WT-PrP. It highlights that the effect of manganese
 on the PrP seems to lie on the incorrectness of the octarepeats numbers. The association of th...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2644808</comments>
            <pubDate>Sat, 25 Jul 2009 14:49:04 +0100</pubDate>
            <guid isPermaLink="false">2644808</guid>        </item>
        <item>
            <title>Tentative identification of glycerol dehydrogenase as Escherichia coli K1 virulence factor cglD and its involvement in the pathogenesis of experimental neonatal meningitis</title>
            <link>http://www.medworm.com/index.php?rid=2605614&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb15u522134142051%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Escherichia coli (E. coli) is the most common gram-negative organism causing meningitis during the neonatal period. The mechanism involved in the pathogenesis
 of E. coli meningitis remains unclear. We previously identified a pathogenicity island GimA (genetic island of meningitic E. coli containing ibeA) from the genomic DNA library of E. coli K1, which may contribute to the E. coli invasion of the blood–brain barrier (BBB). CglD is one of the genes in GimA, and its function remains unknown. In order to characterize the role of cglD in the E. coli meningitis, an isogenic in-frame cglD deletion mutant of E. coli K1 was generated. The results showed that the median lethal dose of the cglD deletion mutant strain was significant higher than that of parent E. coli K1 st...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2605614</comments>
            <pubDate>Tue, 14 Jul 2009 09:57:12 +0100</pubDate>
            <guid isPermaLink="false">2605614</guid>        </item>
        <item>
            <title>Novel swine-origin influenza A virus in humans: another pandemic knocking at the door</title>
            <link>http://www.medworm.com/index.php?rid=2505934&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu65lr3p40n42q1h1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Influenza A viruses represent a continuous pandemic threat. In April 2009, a novel influenza A virus, the so-called swine-origin
 influenza A (H1N1) virus (S-OIV), was identified in Mexico. Although S-OIV originates from triple-reassortant swine influenza
 A (H1) that has been circulating in North American pig herds since the end of the 1990s, S-OIV is readily transmitted between
 humans but is not epidemic in pigs. After its discovery, S-OIV rapidly spread throughout the world within few weeks. In this
 review, we sum up the current situation and put it into the context of the current state of knowledge of influenza and influenza
 pandemics. Some indications suggest that a pandemic may be mild but even “mild” pandemics can result in millions of deaths.
 However, no...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2505934</comments>
            <pubDate>Sat, 20 Jun 2009 06:01:39 +0100</pubDate>
            <guid isPermaLink="false">2505934</guid>        </item>
        <item>
            <title>Single domain antibodies: promising experimental and therapeutic tools in infection and immunity</title>
            <link>http://www.medworm.com/index.php?rid=2505935&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F38l0216lw10064n0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Antibodies are important tools for experimental research and medical applications. Most antibodies are composed of two heavy
 and two light chains. Both chains contribute to the antigen-binding site which is usually flat or concave. In addition to
 these conventional antibodies, llamas, other camelids, and sharks also produce antibodies composed only of heavy chains. The
 antigen-binding site of these unusual heavy chain antibodies (hcAbs) is formed only by a single domain, designated VHH in
 camelid hcAbs and VNAR in shark hcAbs. VHH and VNAR are easily produced as recombinant proteins, designated single domain
 antibodies (sdAbs) or nanobodies. The CDR3 region of these sdAbs possesses the extraordinary capacity to form long fingerlike
 extensions that can extend into ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2505935</comments>
            <pubDate>Tue, 16 Jun 2009 05:50:18 +0100</pubDate>
            <guid isPermaLink="false">2505935</guid>        </item>
        <item>
            <title>Human immunodeficiency virus: 25 years of diagnostic and therapeutic strategies and their impact on hepatitis B and C virus</title>
            <link>http://www.medworm.com/index.php?rid=3100210&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flg94375mn0q61723%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The human immunodeficiency virus (HIV) had spread unrecognized in the human population as sexually transmitted disease and
 was finally identified by its disease AIDS in 1981. Even after the isolation of the causative agent in 1983, the burden and
 death rate of AIDS accelerated worldwide especially in young people despite the confection of new drugs capable to inhibit
 virus replication since 1997. However, at least in industrialised countries, this trend could be reversed by the introduction
 of combination therapy strategies. The design of new drugs is on going; besides the inhibition of the three enzymes of HIV
 for replication and maturation (reverse transcriptase, integrase and protease), further drugs inhibits fusion of viral and
 cellular membranes and virus mat...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3100210</comments>
            <pubDate>Thu, 04 Jun 2009 10:05:52 +0100</pubDate>
            <guid isPermaLink="false">3100210</guid>        </item>
        <item>
            <title>Human immunodeficiency virus: 25 years of diagnostic and therapeutic strategies and their impact on hepatitis B and C virus</title>
            <link>http://www.medworm.com/index.php?rid=2462826&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flg94375mn0q61723%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The human immunodeficiency virus (HIV) had spread unrecognized in the human population as sexually transmitted disease and
 was finally identified by its disease AIDS in 1981. Even after the isolation of the causative agent in 1983, the burden and
 death rate of AIDS accelerated worldwide especially in young people despite the confection of new drugs capable to inhibit
 virus replication since 1997. However, at least in industrialised countries, this trend could be reversed by the introduction
 of combination therapy strategies. The design of new drugs is on going; besides the inhibition of the three enzymes of HIV
 for replication and maturation (reverse transcriptase, integrase and protease), further drugs inhibits fusion of viral and
 cellular membranes and virus mat...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2462826</comments>
            <pubDate>Thu, 04 Jun 2009 10:05:52 +0100</pubDate>
            <guid isPermaLink="false">2462826</guid>        </item>
        <item>
            <title>RfaB, a galactosyltransferase, contributes to the resistance to detergent and the virulence of Salmonella enterica serovar Enteritidis</title>
            <link>http://www.medworm.com/index.php?rid=2387504&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn05x1803341qt3qp%2F</link>
            <description>In this study, a deletion mutant of rfaB (ΔrfaB) was observed to be susceptible to sodium dodecyl sulfate and less tolerant to bile salts. In addition, pre-incubation in
 10% bile salts increased bacterial tolerance to 30% bile salts. We also showed that the ΔrfaB mutant invaded HeLa cells less than the wild type and resulted in a lower ratio of intracellular bacteria. Competitive infection
 of mice showed that the ΔrfaB mutant was defective in the colonization of host organs and was cleared more quickly in fecal shedding. Transforming of a
 plasmid containing a wild-type allele of rfaB (pRB3-rfaB) partially rescued the defect of the ΔrfaB mutant. The results suggest that RfaB, which is responsible to add the glycosyl residue to the core lipopolysaccharide, contributes
 to the toleranc...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2387504</comments>
            <pubDate>Thu, 30 Apr 2009 06:03:31 +0100</pubDate>
            <guid isPermaLink="false">2387504</guid>        </item>
        <item>
            <title>What determines the success or failure of intracellular cutaneous parasites? Lessons learned from leishmaniasis</title>
            <link>http://www.medworm.com/index.php?rid=2375130&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj4355t021m525047%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Most parasitic skin infections are averted by very efficient strategies of preventing pathogen invasion. Innate immune cells
 such as mast cells, macrophages and dendritic cells are responsible for detecting parasites and for recruiting proinflammatory
 cells that help to contain and control the pathogen at sites of infection. This induces efficient adaptive immunity, which
 is crucially important for parasite control. Using the example of cutaneous leishmaniasis, we highlight how the skin utilizes
 different strategies to prevent skin infection and how containment of the infection to the skin site may reduce the harm that
 otherwise may result for the entire organism.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-009-0114-9Authors
		Marcus Maurer, Ch...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2375130</comments>
            <pubDate>Sat, 25 Apr 2009 07:28:20 +0100</pubDate>
            <guid isPermaLink="false">2375130</guid>        </item>
        <item>
            <title>Nitric oxide participation in granulomatous response induced by Paracoccidioides brasiliensis infection in mice</title>
            <link>http://www.medworm.com/index.php?rid=2340998&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F45u038636j36t41l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of nitric oxide (NO) in granulomas of Paracoccidioides brasiliensis-infected inducible NO synthase-deficient C57BL/6 mice (iNOS KO) and their wild-type counterparts and its association with
 osteopontin (OPN) and matrix metalloproteinases (MMPs) was studied. At 15&amp;nbsp;days after infection (DAI), iNOS KO mice showed
 compact and necrotic granulomas with OPN+ macrophages and multinucleated giant cells, whereas wild-type mice developed loose
 granulomas with many fungi and OPN+ cells distributed throughout the tissue. In addition, high OPN levels and fungal load
 were observed in iNOS KO mice. Both experimental groups had MMP-9 activity. At 120 DAI, iNOS KO had smaller granulomas with
 OPN+ cells, lower OPN levels, lower fungal load and decreased MMP-9 activity c...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2340998</comments>
            <pubDate>Fri, 10 Apr 2009 05:58:24 +0100</pubDate>
            <guid isPermaLink="false">2340998</guid>        </item>
        <item>
            <title>Influence of Pseudomonas aeruginosa quorum sensing signal molecule N-(3-oxododecanoyl) homoserine lactone on mast cells</title>
            <link>http://www.medworm.com/index.php?rid=2505936&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F30535m68l84hn63w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Quorum sensing system is a cell-to-cell communication system that plays a pivotal role in virulence expression in bacteria.
 Recent advances have demonstrated that the Pseudomonas aeruginosa quorum sensing molecule, N-3-oxododecanoyl homoserine lactone (3OC12-HSL), exerts effects on mammalian cells and modulates host immune response. Mast cells (MCs) are strategically located in
 the tissues that are constantly exposed to external stimulus. Therefore, it is very much possible that 3OC12-HSL may interact with MCs. Little is known, however, about specific effects of 3OC12-HSL on MCs. To address this, we investigated the influence of 3OC12-HSL on cell viability, apoptosis, intracellular calcium and cytokine release in MCs. We found that at high concentrations
 (100&amp;nbsp;μ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2505936</comments>
            <pubDate>Wed, 01 Apr 2009 05:52:13 +0100</pubDate>
            <guid isPermaLink="false">2505936</guid>        </item>
        <item>
            <title>Influence of 
 Pseudomonas aeruginosa
 quorum sensing signal molecule 
 N
 -(3-oxododecanoyl) homoserine lactone on mast cells</title>
            <link>http://www.medworm.com/index.php?rid=2340999&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F30535m68l84hn63w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Quorum sensing system is a cell-to-cell communication system that plays a pivotal role in virulence expression in bacteria.
 Recent advances have demonstrated that the Pseudomonas aeruginosa quorum sensing molecule, N-3-oxododecanoyl homoserine lactone (3OC12-HSL), exerts effects on mammalian cells and modulates host immune response. Mast cells (MCs) are strategically located in
 the tissues that are constantly exposed to external stimulus. Therefore, it is very much possible that 3OC12-HSL may interact with MCs. Little is known, however, about specific effects of 3OC12-HSL on MCs. To address this, we investigated the influence of 3OC12-HSL on cell viability, apoptosis, intracellular calcium and cytokine release in MCs. We found that at high concentrations
 (100&amp;nbsp;μ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2340999</comments>
            <pubDate>Wed, 01 Apr 2009 05:52:13 +0100</pubDate>
            <guid isPermaLink="false">2340999</guid>        </item>
        <item>
            <title>Diagnostic value of HCMV pp65 antigen detection by FCA for symptomatic and asymptomatic infection: compared to quantification of HCMV DNA and detection of IgM antibody in infants</title>
            <link>http://www.medworm.com/index.php?rid=2297708&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F83575852j28424h2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Human cytomegalovirus (HCMV) can cause symptomatic or asymptomatic infection in infants. One hundred and twenty-six infants
 were assessed clinically for disease in infantile period. Eighty of them were classified as symptomatic infection on the basis
 of physical, instrumental, and laboratory findings, 5 were demonstrated by following up to have later developed HCMV disease,
 and the other 41 infants were classified as asymptomatic infection. HCMV DNA was positive in all urine samples of the symptomatic
 infants detected by quantitative polymerase chain reaction. HCMV-IgM antibody detected by chemiluminescent immunoassay (CLIA)
 was positive in 62 of the 85 symptomatic infants, but was negative in all of the samples of asymptomatic infants. HCMV pp65
 antigen detected ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2297708</comments>
            <pubDate>Tue, 24 Mar 2009 07:08:37 +0100</pubDate>
            <guid isPermaLink="false">2297708</guid>        </item>
        <item>
            <title>No evidence of chikungunya virus and antibodies shortly before the outbreak on Sri Lanka</title>
            <link>http://www.medworm.com/index.php?rid=2199458&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F55w112254241l461%2F</link>
            <description>This study
 determined the prevalence of anti-CHIKV IgG antibodies as well as CHIKV RNA shortly before the outbreak. Two hundred and six
 human sera were collected from patients with acute febrile illness in 2004/2005. Validated indirect immunofluorescence and
 real-time RT-PCR assays for dengue as well as CHIKV were employed. Laboratory evidence of dengue virus infection was seen
 in 67% of patients, indicating virus activity and exposure to Aedes spp. vectors. These vectors are the same as for chikungunya. However, no evidence of acute or previous chikungunya infection
 could be demonstrated in the same cohort. This study gives formal evidence that the absence of human population immunity correlated
 with a large chikungunya epidemic.
 
	Content Type Journal ArticleCategory Original Inve...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2199458</comments>
            <pubDate>Wed, 18 Feb 2009 08:50:46 +0100</pubDate>
            <guid isPermaLink="false">2199458</guid>        </item>
        <item>
            <title>Buruli ulcer disease: prospects for a vaccine</title>
            <link>http://www.medworm.com/index.php?rid=2172078&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F687607660003911u%2F</link>
            <description>This article reviews the present state of the art with special emphasis on the immunology of the infection and the prospects
 for development of a vaccine.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-009-0109-6Authors
		Kris Huygen, Scientific Institute of Public Health Rue Engelandstraat 642 1180 Brussels BelgiumOhene Adjei, Kumasi Centre for Collaborative Research Kumasi GhanaDissou Affolabi, Laboratoire de Référence des Mycobactéries Cotonou BeninGisela Bretzel, Ludwig-Maximilians-University Department of Infectious Diseases and Tropical Medicine Munich GermanyCaroline Demangel, Institut Pasteur Paris FranceBernhard Fleischer, Bernhard Nocht Institute for Tropical Medicine Hamburg GermanyRoch Christian Johnson, Programme National de Lutte contre l’Ulcère de Bu...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2172078</comments>
            <pubDate>Sat, 07 Feb 2009 10:10:10 +0100</pubDate>
            <guid isPermaLink="false">2172078</guid>        </item>
        <item>
            <title>Oncomodulation by human cytomegalovirus: evidence becomes stronger</title>
            <link>http://www.medworm.com/index.php?rid=2172077&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe87w53748n883l66%2F</link>
            <description>Content Type Journal ArticleCategory Mini ReviewDOI 10.1007/s00430-009-0107-8Authors
		Martin Michaelis, Klinikum der Johann Wolfgang Goethe-Universität Institut für Medizinische Virologie Paul Ehrlich-Str. 40 60596 Frankfurt am Main GermanyHans Wilhelm Doerr, Klinikum der Johann Wolfgang Goethe-Universität Institut für Medizinische Virologie Paul Ehrlich-Str. 40 60596 Frankfurt am Main GermanyJindrich Cinatl, Klinikum der Johann Wolfgang Goethe-Universität Institut für Medizinische Virologie Paul Ehrlich-Str. 40 60596 Frankfurt am Main Germany
	

	
		Journal Medical Microbiology and ImmunologyOnline ISSN 1432-1831Print ISSN 0300-8584 (Source: Medical Microbiology and Immunology)</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2172077</comments>
            <pubDate>Sat, 07 Feb 2009 10:10:10 +0100</pubDate>
            <guid isPermaLink="false">2172077</guid>        </item>
        <item>
            <title>Seroprevalence of influenza A and B in German infants and adolescents</title>
            <link>http://www.medworm.com/index.php?rid=2166853&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq111g88615088512%2F</link>
            <description>In conclusion,
 the annual influenza vaccination in children and adolescents may improve considerably the protection against influenza virus
 infection occurring during epidemics.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-009-0108-7Authors
		Andreas Sauerbrei, Friedrich-Schiller University of Jena Institute of Virology and Antiviral Therapy Hans-Knoell-Strasse 2 07745 Jena GermanyR. Schmidt-Ott, GlaxoSmithKline Theresienhöhe 11 80339 Munich GermanyH. Hoyer, Institute for Medical Statistics, Computer Sciences and Documentation Bachstrasse 18 07743 Jena GermanyP. Wutzler, Friedrich-Schiller University of Jena Institute of Virology and Antiviral Therapy Hans-Knoell-Strasse 2 07745 Jena Germany
	

	
		Journal Medical Microbiology and ImmunologyOnline ISS...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2166853</comments>
            <pubDate>Thu, 05 Feb 2009 06:51:18 +0100</pubDate>
            <guid isPermaLink="false">2166853</guid>        </item>
        <item>
            <title>Seroepidemiological study in a Puumala virus outbreak area in South-East Germany</title>
            <link>http://www.medworm.com/index.php?rid=2505937&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq2x821375500h751%2F</link>
            <description>In conclusion, the PUUV seroprevalence
 in the residents of the outbreak region in Lower Bavaria was found to be up to fivefold higher than the average hantavirus
 seroprevalence of the German population.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-009-0106-9Authors
		Marc Mertens, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, OIE Collaborating Centre for Zoonoses in Europe, Institute for Novel and Emerging Infectious Diseases Südufer 10 17493 Greifswald, Insel Riems GermanyRoman Wölfel, Bundeswehr Institute of Microbiology 80937 Munich GermanyKatrin Ullrich, Institute of Epidemiology 16868 Wusterhausen GermanyKumiko Yoshimatsu, Institute for Animal Experimentation, Hokkaido University Graduate School of Medicine Sapporo J...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2505937</comments>
            <pubDate>Fri, 16 Jan 2009 12:47:08 +0100</pubDate>
            <guid isPermaLink="false">2505937</guid>        </item>
        <item>
            <title>Seroepidemiological study in a 
 Puumala virus
 outbreak area in South-East Germany</title>
            <link>http://www.medworm.com/index.php?rid=2111966&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq2x821375500h751%2F</link>
            <description>In conclusion, the PUUV seroprevalence
 in the residents of the outbreak region in Lower Bavaria was found to be up to fivefold higher than the average hantavirus
 seroprevalence of the German population.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-009-0106-9Authors
		Marc Mertens, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, OIE Collaborating Centre for Zoonoses in Europe, Institute for Novel and Emerging Infectious Diseases Südufer 10 17493 Greifswald, Insel Riems GermanyRoman Wölfel, Bundeswehr Institute of Microbiology 80937 Munich GermanyKatrin Ullrich, Institute of Epidemiology 16868 Wusterhausen GermanyKumiko Yoshimatsu, Institute for Animal Experimentation, Hokkaido University Graduate School of Medicine Sapporo J...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2111966</comments>
            <pubDate>Fri, 16 Jan 2009 12:47:08 +0100</pubDate>
            <guid isPermaLink="false">2111966</guid>        </item>
        <item>
            <title>A Neisseria meningitidis NMB1966 mutant is impaired for invasion of respiratory epithelial cells, survival in human blood and for virulence in vivo</title>
            <link>http://www.medworm.com/index.php?rid=3100211&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw2qv4255w2g417w3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We sought to determine whether NMB1966, encoding a putative ABC transporter, has a role in pathogenesis. Compared to its isogenic
 wild-type parent strain Neisseria meningitidis MC58, the NMB1966 knockout mutant was less adhesive and invasive for human bronchial epithelial cells, had reduced survival
 in human blood and was attenuated in a systemic mouse model of infection. The transcriptome of the wild-type and the NMB1966
 mutant was compared. The data are consistent with a previous functional assignment of NMB1966 being the ABC transporter component
 of a glutamate transporter operon. Forty-seven percent of all the differentially regulated genes encoded known outer membrane
 proteins or pathways generating complex surface structures such as adhesins, peptidoglycan an...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3100211</comments>
            <pubDate>Wed, 03 Dec 2008 08:26:34 +0100</pubDate>
            <guid isPermaLink="false">3100211</guid>        </item>
        <item>
            <title>A 
 Neisseria meningitidis
 NMB1966 mutant is impaired for invasion of respiratory epithelial cells, survival in human blood and for virulence in vivo</title>
            <link>http://www.medworm.com/index.php?rid=2013148&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw2qv4255w2g417w3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We sought to determine whether NMB1966, encoding a putative ABC transporter, has a role in pathogenesis. Compared to its isogenic
 wild-type parent strain Neisseria meningitidis MC58, the NMB1966 knockout mutant was less adhesive and invasive for human bronchial epithelial cells, had reduced survival
 in human blood and was attenuated in a systemic mouse model of infection. The transcriptome of the wild-type and the NMB1966
 mutant was compared. The data are consistent with a previous functional assignment of NMB1966 being the ABC transporter component
 of a glutamate transporter operon. Forty-seven percent of all the differentially regulated genes encoded known outer membrane
 proteins or pathways generating complex surface structures such as adhesins, peptidoglycan an...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2013148</comments>
            <pubDate>Wed, 03 Dec 2008 08:26:34 +0100</pubDate>
            <guid isPermaLink="false">2013148</guid>        </item>
        <item>
            <title>Comparison of performance in two diagnostic methods for tuberculosis infection</title>
            <link>http://www.medworm.com/index.php?rid=1995724&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk858344102220163%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Performance of two diagnoses, T-SPOT®.TB (T-SPOT) and QuantiFERON-TB® Gold (QFT-G), was compared in Japanese subjects. Forty-seven confirmed tuberculosis patients and eighty-four healthy subjects
 were recruited. All samples were assessed for both T-SPOT and QFT-G, and the sensitivities and the specificities were compared
 between two methods. The sensitivity was 100% for T-SPOT, and 87.2% for QFT-G. The specificity was 83.3 and 98.8%, respectively.
 The overall agreement of two tests was substantially high (Kappa coefficient&amp;nbsp;=&amp;nbsp;0.671). The sensitivity of T-SPOT appeared
 to be higher than that of QFT-G, whereas the specificity of T-SPOT was significantly lower than that of QFT-G. The difference
 in the performance between T-SPOT and QFT-G and biological rele...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1995724</comments>
            <pubDate>Wed, 26 Nov 2008 19:59:58 +0100</pubDate>
            <guid isPermaLink="false">1995724</guid>        </item>
        <item>
            <title>Characterization of Gag and Nef-specific ELISpot-based CTL responses in HIV-1 infected Indian individuals</title>
            <link>http://www.medworm.com/index.php?rid=1944872&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb7mrk2648m841131%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cytotoxic T lymphocyte (CTL) responses to Gag have been most frequently linked to control of viremia whereas CTL responses
 to Nef have direct relationship with viral load. IFN-γ ELISpot assay was used to screen CTL responses at single peptide level
 directed at HIV-1 subtype C Gag and Nef proteins in 30 antiretroviral therapy naive HIV-1 infected Indian individuals. PBMCs
 from 73.3% and 90% of the study population showed response to Gag and Nef antigens, respectively. The magnitude of Gag-specific
 CTL responses was inversely correlated with plasma viral load (r&amp;nbsp;=&amp;nbsp;−0.45, P&amp;nbsp;=&amp;nbsp;0.001), whereas magnitude of Nef-specific responses was directly correlated (r&amp;nbsp;=&amp;nbsp;0.115). Thirteen immunodominant regions (6 in Gag, 7 in Nef) were identified in th...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1944872</comments>
            <pubDate>Thu, 06 Nov 2008 00:34:16 +0100</pubDate>
            <guid isPermaLink="false">1944872</guid>        </item>
        <item>
            <title>The bradykinin B2 receptor in the early immune response against Listeria infection</title>
            <link>http://www.medworm.com/index.php?rid=3100212&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F42k7mq83711u14w3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The endogenous danger signal bradykinin was recently found implicated in the development of immunity against parasites via
 dendritic cells. We here report an essential role of the B2 (B2R) bradykinin receptor in the early immune response against Listeria infection. Mice deficient in B2R (B2R−/− mice) were shown to suffer from increased hepatic bacterial burden and concomitant dramatic weight loss during infection
 with Listeria monocytogenes. Levels of cytokines known to play a pivotal role in the early phase immune response against L. monocytogenes, IL-12p70 and IFN-γ, were reduced in B2R−/− mice. To extend these findings to the human system, we show that bradykinin potentiates the production of IL-12p70 in human
 monocyte-derived dendritic cells. Thus, we sh...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3100212</comments>
            <pubDate>Tue, 23 Sep 2008 10:15:04 +0100</pubDate>
            <guid isPermaLink="false">3100212</guid>        </item>
        <item>
            <title>The bradykinin B2 receptor in the early immune response against 
 Listeria
 infection</title>
            <link>http://www.medworm.com/index.php?rid=1824029&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F42k7mq83711u14w3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The endogenous danger signal bradykinin was recently found implicated in the development of immunity against parasites via
 dendritic cells. We here report an essential role of the B2 (B2R) bradykinin receptor in the early immune response against Listeria infection. Mice deficient in B2R (B2R−/− mice) were shown to suffer from increased hepatic bacterial burden and concomitant dramatic weight loss during infection
 with Listeria monocytogenes. Levels of cytokines known to play a pivotal role in the early phase immune response against L. monocytogenes, IL-12p70 and IFN-γ, were reduced in B2R−/− mice. To extend these findings to the human system, we show that bradykinin potentiates the production of IL-12p70 in human
 monocyte-derived dendritic cells. Thus, we sh...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1824029</comments>
            <pubDate>Tue, 23 Sep 2008 10:15:04 +0100</pubDate>
            <guid isPermaLink="false">1824029</guid>        </item>
        <item>
            <title>Inhibition of HBV infection by bovine lactoferrin and iron-, zinc-saturated lactoferrin</title>
            <link>http://www.medworm.com/index.php?rid=1824028&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl6w5008632010082%2F</link>
            <description>In conclusion, BLf, iron- or zinc-saturated
 BLf is one of the candidates for anti-HBV reagents in treatment of patients with hepatitis.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-008-0100-7Authors
		Songtao Li, Northeast Agricultural University Key Laboratory of Dairy Science, Ministry of Education; College of Food Science 150030 Harbin Heilongjiang ChinaHaibo Zhou, Northeast Agricultural University Key Laboratory of Dairy Science, Ministry of Education; College of Food Science 150030 Harbin Heilongjiang ChinaGuirong Huang, Harbin Medical University Staff Room of Epidemiology, College of Public Health 150086 Harbin Heilongjiang ChinaNing Liu, Northeast Agricultural University Key Laboratory of Dairy Science, Ministry of Education; College of Food Scie...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1824028</comments>
            <pubDate>Tue, 23 Sep 2008 10:15:04 +0100</pubDate>
            <guid isPermaLink="false">1824028</guid>        </item>
        <item>
            <title>Immune complexed (IC) hepatitis C virus (HCV) in chronically and acutely HCV-infected patients</title>
            <link>http://www.medworm.com/index.php?rid=1704394&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9212r6w447633633%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In infected individuals, hepatitis C virus (HCV) exists in various forms of circulating particles which role in virus persistence
 and in HCV resistance to IFN therapy is still debated. Here, the proportion of HCV bound to immunoglobulin was determined
 in plasma of 107 chronically infected patients harbouring different HCV genotypes and, for comparison, of six patients with
 acute HCV infection. The results showed that, in spite of wide individual variability, chronically HCV-infected patients exhibited
 an extremely high proportion of immune complexed (IC) virus regardless of plasma HCV load and infecting genotype. Moreover,
 no significant association was found between baseline proportion of IC HCV and response to IFN treatment. Plasma samples collected
 within 2&amp;nbs...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1704394</comments>
            <pubDate>Tue, 12 Aug 2008 07:29:27 +0100</pubDate>
            <guid isPermaLink="false">1704394</guid>        </item>
        <item>
            <title>Inhibition of hepatitis B virus replication by small interference RNA induces expression of MICA in HepG2.2.15 cells</title>
            <link>http://www.medworm.com/index.php?rid=1691477&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3527k1v657743j23%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hepatitis B virus (HBV) replicates in most tumor tissues of patients with HBV-associated hepatocellular carcinoma (HCC). In
 the present study, we have shown that the expression of HBV in the HCC cell lines, HepG2 and Huh7, down-regulated the expression
 of MHC class I-related molecule A (MICA), a ligand of the NKG2D receptor. Inhibition of HBV expression by small interference
 RNAs (siRNAs) in HepG2.2.15, a cell line that constitutively expresses HBV, induced up-regulation of MICA. The up-regulation
 of MICA increased the lysis of HepG2.2.15 cells by NK cells. Our results suggest that HBV compromises the innate immune system
 in HCC patients and that inhibition of HBV replication by siRNAs may enhance the antitumor immune response.
 
	Content Type Journal ArticleCatego...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1691477</comments>
            <pubDate>Thu, 07 Aug 2008 09:59:48 +0100</pubDate>
            <guid isPermaLink="false">1691477</guid>        </item>
        <item>
            <title>HLA class I alleles in HTLV-1-associated myelopathy and asymptomatic carriers from the Brazilian cohort GIPH</title>
            <link>http://www.medworm.com/index.php?rid=1493987&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5271576t731kq978%2F</link>
            <description>Discussion&amp;nbsp;&amp;nbsp;The presence of HLA-A2 elicits a stronger cytotoxic response, which is involved in the HTLV-1 proviral load reduction. This
 study confirmed a tendency of this allele to protect against HAM-TSP. Therefore, A*02 might be of interest for researches
 involved with HTLV-1 vacine.
 
 
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-008-0096-zAuthors
		B. C. Catalan-Soares, Fundação Hemominas Rua Grão Pará, 882 Belo Horizonte Minas Gerais 30.150-340 BrazilAnna Bárbara F. Carneiro-Proietti, Fundação Hemominas Rua Grão Pará, 882 Belo Horizonte Minas Gerais 30.150-340 BrazilF. G. Da Fonseca, Centro de Pesquisas René Rachou (Fiocruz) Belo Horizonte Minas Gerais BrazilR. Correa-Oliveira, Centro de Pesquisas René Rachou (Fiocruz) Belo H...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1493987</comments>
            <pubDate>Tue, 03 Jun 2008 06:19:03 +0100</pubDate>
            <guid isPermaLink="false">1493987</guid>        </item>
        <item>
            <title>Evaluation of a recombinant BCG expressing antigen Ag85B and PPE protein Rv3425 from DNA segment RD11 of Mycobacterium tuberculosis in C57BL/6 mice</title>
            <link>http://www.medworm.com/index.php?rid=3100213&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg41505071054j180%2F</link>
            <description>In this study we constructed a new rBCG which included this united gene (Ag85B-Rv3425). The level
 of antigen-stimulated T cells expressing IFN-γ was significantly higher in the C57BL/6 mice vaccinated with rBCG::Ag85B-Rv3425
 than with BCG. In addition, the sera from mice immunized with rBCG::Ag85B-Rv3425 revealed an increase in the specific immunoglobulin
 G titers than that from mice immunized with BCG. Antigen specific IgG subclass analysis showed that rBCG::Ag85B-Rv3425 tended
 to facilitate IgG2a production, suggesting enhancement of predominant Th1 response which in turn may facilitate increased
 production of protective IFN-γ. These results suggested that this rBCG::Ag85B-Rv3425 could be a strong vaccine candidate for
 further study.
 
	Content Type Journal ArticleCategory Origin...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3100213</comments>
            <pubDate>Tue, 20 May 2008 06:17:14 +0100</pubDate>
            <guid isPermaLink="false">3100213</guid>        </item>
        <item>
            <title>Evaluation of a recombinant BCG expressing antigen Ag85B and PPE protein Rv3425 from DNA segment RD11 of 
 Mycobacterium tuberculosis
 in C57BL/6 mice</title>
            <link>http://www.medworm.com/index.php?rid=1463254&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg41505071054j180%2F</link>
            <description>In this study we constructed a new rBCG which included this united gene (Ag85B-Rv3425). The level
 of antigen-stimulated T cells expressing IFN-γ was significantly higher in the C57BL/6 mice vaccinated with rBCG::Ag85B-Rv3425
 than with BCG. In addition, the sera from mice immunized with rBCG::Ag85B-Rv3425 revealed an increase in the specific immunoglobulin
 G titers than that from mice immunized with BCG. Antigen specific IgG subclass analysis showed that rBCG::Ag85B-Rv3425 tended
 to facilitate IgG2a production, suggesting enhancement of predominant Th1 response which in turn may facilitate increased
 production of protective IFN-γ. These results suggested that this rBCG::Ag85B-Rv3425 could be a strong vaccine candidate for
 further study.
 
	Content Type Journal ArticleCategory Origin...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1463254</comments>
            <pubDate>Tue, 20 May 2008 06:17:14 +0100</pubDate>
            <guid isPermaLink="false">1463254</guid>        </item>
        <item>
            <title>Characterization and intracellular localization of putative Chlamydia pneumoniae effector proteins</title>
            <link>http://www.medworm.com/index.php?rid=3096367&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm822237139q7r512%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We here describe four proteins of Chlamydia pneumoniae, which might play a role in host-pathogen interaction. The hypothetical bacterial proteins CPn0708 and CPn0712 were detected
 in Chlamydia pneumoniae-infected host cells by indirect immunofluorescence tests with polyclonal antisera raised against the respective proteins.
 While CPn0708 was localized within the inclusion body, CPn0712 was identified in the inclusion membrane and in the surrounding
 host cell cytosol. CPn0712 colocalizes with actin, indicating its possible interaction with components of the cytoskeleton.
 Investigations on CPn0809 and CPn1020, two Chlamydia pneumoniae proteins previously described to be secreted into the host cell cytosol, revealed colocalization with calnexin, a marker
 for the ER. N...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3096367</comments>
            <pubDate>Thu, 01 May 2008 06:28:35 +0100</pubDate>
            <guid isPermaLink="false">3096367</guid>        </item>
        <item>
            <title>Characterization and intracellular localization of putative 
 Chlamydia pneumoniae
 effector proteins</title>
            <link>http://www.medworm.com/index.php?rid=1417426&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm822237139q7r512%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We here describe four proteins of Chlamydia pneumoniae, which might play a role in host-pathogen interaction. The hypothetical bacterial proteins CPn0708 and CPn0712 were detected
 in Chlamydia pneumoniae-infected host cells by indirect immunofluorescence tests with polyclonal antisera raised against the respective proteins.
 While CPn0708 was localized within the inclusion body, CPn0712 was identified in the inclusion membrane and in the surrounding
 host cell cytosol. CPn0712 colocalizes with actin, indicating its possible interaction with components of the cytoskeleton.
 Investigations on CPn0809 and CPn1020, two Chlamydia pneumoniae proteins previously described to be secreted into the host cell cytosol, revealed colocalization with calnexin, a marker
 for the ER. N...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1417426</comments>
            <pubDate>Thu, 01 May 2008 06:28:35 +0100</pubDate>
            <guid isPermaLink="false">1417426</guid>        </item>
        <item>
            <title>Does the proper intravenous immunoglobulin substitution in primary immunodeficiency protect against HBV infections?: a description of a case series</title>
            <link>http://www.medworm.com/index.php?rid=1362197&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy4223h766v59850p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 There are no recommendations concerning preoperative management of primary immunodeficiency patients in cases of emergency
 or planned surgery in relation to risk of hepatitis type B virus infection. To assess if immunodeficient patients regularly
 supplemented with immunoglobulins are protected against hepatitis B. IgG, IgM and IgA total levels and anti-HBs level were
 estimated in adult patients with primary humoral immunodeficiency before and after immunoglobulins supplementation according
 to a standardized schedule. Serum IgG and anti-HBs level significantly increased after immunoglobulin supplementation. Anti-HBs
 titer increased in all cases over 100&amp;nbsp;IU/L regardless of initial total IgG serum value, reaching a highly protective level.
 There was no correla...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1362197</comments>
            <pubDate>Tue, 08 Apr 2008 07:25:17 +0100</pubDate>
            <guid isPermaLink="false">1362197</guid>        </item>
        <item>
            <title>Hematopoietic stem cell transplantation with latently infected donors does not transmit virus to immunocompromised recipients in the murine model of cytomegalovirus infection</title>
            <link>http://www.medworm.com/index.php?rid=1331160&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj086k7h7550v6k67%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hematopoietic stem cell transplantation (HSCT) bears a risk of reactivating latent cytomegalovirus (CMV) in either the transplanted
 hematopoietic donor cells or in parenchymal and stromal tissue cells of the immunocompromised recipient, or in both. While
 reactivated human CMV in recipients of organ transplantations is frequently the virus variant of the donor, this is not usually
 the case in HSCT recipients. Here we have used experimental sex-mismatched HSCT in the BALB/c mouse model to test if latent
 murine CMV from CMV-immune donors is transmitted with bone marrow cells to naive immunocompromised recipients.
 
	Content Type Journal ArticleCategory Original InvestigationDOI 10.1007/s00430-008-0094-1Authors
		Christof K. Seckert, Johannes Gutenberg-University Instit...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1331160</comments>
            <pubDate>Wed, 26 Mar 2008 14:52:27 +0100</pubDate>
            <guid isPermaLink="false">1331160</guid>        </item>
        <item>
            <title>Polyclonal cytomegalovirus-specific antibodies not only prevent virus dissemination from the portal of entry but also inhibit focal virus spread within target tissues</title>
            <link>http://www.medworm.com/index.php?rid=1331159&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftl65q241481g0x17%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Therapy of cytomegalovirus (CMV) infection in recipients of hematopoietic stem cell transplantation (HSCT) by immune serum
 transfer did not fulfill the high clinical expectations, although immune sera or immunoglobulin-enriched preparations pooled
 from many CMV-immune donors are likely to contain virus neutralizing antibodies covering a broad range of virus variants.
 Likewise, the highest risk of CMV disease in HSCT recipients results from the reactivation of the latently infected recipient’s
 own virus despite pre-transplantation humoral immunity. These findings suggest the conclusion that antiviral antibodies are
 inefficient in controlling CMV. Rather than B cells and antibodies, T cells, in particular CD8 T cells, are thought to play
 a major role in resolving ...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1331159</comments>
            <pubDate>Wed, 26 Mar 2008 14:52:27 +0100</pubDate>
            <guid isPermaLink="false">1331159</guid>        </item>
        <item>
            <title>Characterisation of a chikungunya virus from a German patient returning from Mauritius and development of a serological test</title>
            <link>http://www.medworm.com/index.php?rid=1318982&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa741k66065j0v55n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have isolated a Chikungunya (Chik) virus from a patient who returned to Germany after a three-month visit to Mauritius
 in spring 2006. Upon return she developed a transient fever up to 40°C. This was followed by myalgia and joint pain. IgG antibodies
 in serum to Chik virus were undetectable. Virus (Chik-Wü1) was isolated on Vero cells. We molecularly cloned the whole genome
 of Chik-Wü1 from viral RNA by RT-PCR. The complete sequence was determined and functional domains of the genome were assigned.
 Chik-Wü1 clearly belongs to the group of viruses analysed from the recent Indian Ocean outbreak. In order to develop tools
 useful for further characterization of Chik-Wü1, we bacterially expressed and purified the capsid (C) and envelope (E) proteins
 and establi...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1318982</comments>
            <pubDate>Thu, 20 Mar 2008 09:25:24 +0100</pubDate>
            <guid isPermaLink="false">1318982</guid>        </item>
        <item>
            <title>CD8 T-cell-based immunotherapy of cytomegalovirus infection: “proof of concept” provided by the murine model</title>
            <link>http://www.medworm.com/index.php?rid=1307521&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft5w63758545l5613%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adoptive transfer of antiviral effector or memory CD8 T cells is a therapeutic option for preventing acute cytomegalovirus
 (CMV) disease after primary or recurrent infection in immunocompromised recipients of hematopoietic stem cell transplantation
 (HSCT) aimed at curing hematopoietic malignancies. Preclinical research in murine models has demonstrated the power of CD8
 T-cell-based preemptive immunotherapy and has encouraged clinical trials that gave promising results. The clinical evidence,
 however, is based primarily on statistical analyses indicating a reduced incidence of CMV-associated complications. Here,
 we will briefly review the data obtained from the murine model showing that CD8 T cells derived from CMV-immune donors and
 administered either as peptide-s...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1307521</comments>
            <pubDate>Sat, 15 Mar 2008 09:14:38 +0100</pubDate>
            <guid isPermaLink="false">1307521</guid>        </item>
        <item>
            <title>Correlation of dendritic cell maturation and the formation of aggregates of poly-ubiquitinated proteins in the cytosol</title>
            <link>http://www.medworm.com/index.php?rid=1307522&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F83452721r52u5t7u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Dendritic cells (DCs) are the most powerful antigen presenting cells (APCs) in the immune system. Therefore, they are able
 to take up antigen by phagocytosis, macropinocytosis or endocytosis, process it in the cytosol and present it to naive T cells.
 It is known that presentation of the immunodominant influenza virus nucleoprotein-derived CTL epitope is delayed in bone marrow-derived
 DCs (BMDCs) compared to non-professional APCs. This delay coincided with the formation of transient aggregations of ubiquitinated
 proteins (DALIS, dendritic cell aggresome-like induced structures), which contain probably defective ribosomal products (DRiPs).
 DRiPs appear in the cytosol of maturing DCs and macrophages. Normally, DRiPs are degraded rapidly by proteasomes. However,
 their...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1307522</comments>
            <pubDate>Fri, 14 Mar 2008 07:28:38 +0100</pubDate>
            <guid isPermaLink="false">1307522</guid>        </item>
        <item>
            <title>Epitope-specific in vivo protection against cytomegalovirus disease by CD8 T cells in the murine model of preemptive immunotherapy</title>
            <link>http://www.medworm.com/index.php?rid=1307523&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F083657703n0k7u51%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Preclinical research in murine models as well as subsequent clinical trials have concordantly revealed a high protective potential
 of antiviral CD8 T cells, of donor-derived ex vivo memory CD8 T cells in particular, in the immunotherapy of cytomegalovirus
 (CMV) infection in immunocompromised recipients. Although it is generally held view that the observed beneficial effect of
 the transferred cells is viral epitope-specific, involving the recognition of MHC class-I presented peptides by cognate T
 cell receptors, this assumption awaits formal proof, at least with regard to the in vivo function of the CD8 T cells. This
 question is particularly evident for CMV, since the function of viral immune evasion proteins interferes with the MHC class-I
 pathway of peptide prese...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1307523</comments>
            <pubDate>Fri, 14 Mar 2008 07:28:37 +0100</pubDate>
            <guid isPermaLink="false">1307523</guid>        </item>
        <item>
            <title>MHC class I immune evasion in MCMV infection</title>
            <link>http://www.medworm.com/index.php?rid=1300041&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl4478871721384mv%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Murine cytomegalovirus (MCMV) is a well-studied model of natural β-herpesvirus infection. However, many questions remain regarding
 its control by and evasion of the immune response it generates. CD8 and CD4 T cells have both unique and redundant roles in
 control of the virus that differ based on the immunocompetence of the infected mice. MCMV encodes major histocompatibility
 complex (MHC) class I immune evasion genes that can have an impact in vitro, but their role in infection of immunocompetent
 mice has been difficult to identify. This review addresses the evidence for their in vivo function and suggests why they may
 be evolutionarily conserved.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-008-0089-yAuthors
		Carmen M. Doom, Oregon Health and...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1300041</comments>
            <pubDate>Tue, 11 Mar 2008 08:34:50 +0100</pubDate>
            <guid isPermaLink="false">1300041</guid>        </item>
        <item>
            <title>New tools to study the role of B cells in cytomegalovirus infections</title>
            <link>http://www.medworm.com/index.php?rid=1300040&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvn6322732k3q6762%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;B cells were previously shown to mediate partial protection against CMV infection, as in the absence of B cells, latently
 infected mice were more susceptible to virus reactivation. It remains unclear if this effect stems from the loss of B cells
 as antibody producers or as antigen presenting cells. To address this fundamental question, we propose to make use of new
 mouse models that allow conditional ablation of B cells or that allow for the generation of mice with B cells that are not
 able to produce antibodies.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-008-0088-zAuthors
		Ari Waisman, University of Mainz 1st Medical Department Obere-Zahlbacherstr. 63 55131 Mainz GermanyAndrew L. Croxford, University of Mainz 1st Medical Department Obere-Zahl...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1300040</comments>
            <pubDate>Tue, 11 Mar 2008 08:34:50 +0100</pubDate>
            <guid isPermaLink="false">1300040</guid>        </item>
        <item>
            <title>Human cytomegalovirus infection and antiviral immunity in septic patients without canonical immunosuppression</title>
            <link>http://www.medworm.com/index.php?rid=1289598&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv57k513n265q1q27%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The human cytomegalovirus (HCMV) is a relevant pathogen in patients with immunosuppressive therapy; however, reactivation
 and subsequent recurrence occurs also in individuals without canonical immunosuppression as e.g., in patients with septic
 shock. Analyzing the impact of NK- and T-cell immunity on the natural course of HCMV infection in patients with septic shock,
 it became clear that the presence of HCMV reactive T-helper cells did not prevent the development of reactivation but, the
 control of active infection was achieved mostly by specific T-cells. NK-cells seemed to be dispensable for clearance of active
 infection in this patient group with long-lasting NK-cell anergy.
 
	Content Type Journal ArticleCategory ReviewDOI 10.1007/s00430-008-0087-0Authors
		Lutz...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1289598</comments>
            <pubDate>Sat, 08 Mar 2008 10:05:06 +0100</pubDate>
            <guid isPermaLink="false">1289598</guid>        </item>
        <item>
            <title>Conditional gene expression systems to study herpesvirus biology in vivo</title>
            <link>http://www.medworm.com/index.php?rid=1289599&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1916g66856343q1p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cytomegalovirus (CMV), a prototypic β-herpesvirus, is an important human pathogen causing protean clinical manifestations
 in immature and immunocompromised patients. Mechanisms of infection can be studied in a mouse model. Mouse cytomegalovirus
 (MCMV) resembles in pathogenesis its human counterpart in many ways. Although MCMV infection is studied extensively on the
 level of organs, the contribution of specific cell types to viral replication in vivo is still elusive. Here we describe our
 approach based on the the Cre/loxP-system to investigate MCMV infection at the level of cell types in vivo. Using bacterial artificial chromosome (BAC)-technology,
 we created an MCMV virus containing an enhanced green fluorescent protein (egfp) reporter-gene which is not expressed...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1289599</comments>
            <pubDate>Fri, 07 Mar 2008 06:51:18 +0100</pubDate>
            <guid isPermaLink="false">1289599</guid>        </item>
        <item>
            <title>Refinement of strategies for the development of a human cytomegalovirus dense body vaccine</title>
            <link>http://www.medworm.com/index.php?rid=1284488&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6302u58445031913%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Development of a vaccine against human cytomegalovirus (HCMV) infection has been identified as a high priority goal in biomedical
 research, yet no vaccine has been licensed until now. Recombinant subviral dense bodies (recDB) are a promising basis for
 the establishment of such a vaccine. In this article, strategies for the generation of recDB, based on recombination-mediated
 genetic engineering of the 230&amp;nbsp;kb HCMV DNA genome in E. coli are outlined. Analysis of viral mutants that were constructed in this process provided the proof-of-principle that heterologous
 antigens can be packaged into recDB and that these particles prime CD8 T cell responses against the recombinant antigen upon
 their application to HLA-A2 transgenic mice.
 
	Content Type Journal ArticleCa...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1284488</comments>
            <pubDate>Wed, 05 Mar 2008 07:50:10 +0100</pubDate>
            <guid isPermaLink="false">1284488</guid>        </item>
        <item>
            <title>Activation of hepatic natural killer cells and control of liver-adapted lymphoma in the murine model of cytomegalovirus infection</title>
            <link>http://www.medworm.com/index.php?rid=1272292&amp;cid=s_33326_77_f&amp;fid=33326&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj76314px64223838%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hematopoietic stem cell transplantation (HSCT) is a promising therapeutic option against hematopoietic malignancies. Infection
 with cytomegalovirus (CMV) and tumor relapse are complications that limit the success of HSCT. In theory, CMV infection can
 facilitate tumor relapse and growth by inhibiting “graft take” and reconstitution of the immune system or by inducing the
 secretion of tumor cell growth-promoting cytokines. Conversely, one can also envisage an anti-tumoral effect of CMV by cytopathic/oncolytic
 infection of tumor cells, by inducing the secretion of death ligands for tumor cell apoptosis, and by the activation of systemic
 innate and adaptive immunity. Here we will briefly review the current knowledge about tumor control in a murine model of CMV
 inf...</description>
            <author>Medical Microbiology and Immunology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1272292</comments>
            <pubDate>Fri, 29 Feb 2008 09:35:05 +0100</pubDate>
            <guid isPermaLink="false">1272292</guid>        </item>
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