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        <title>Current HIV Research 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 'Current HIV Research' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Current+HIV+Research&t=Current+HIV+Research&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 18:15:39 +0100</lastBuildDate>
        <item>
            <title>Future Prospects and Perspectives on Microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626536&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264086%26dopt%3DAbstract</link>
            <description>Authors: Anton PA
    Abstract
    As 'proof of concept' has now been well validated for topical microbicides, the progress has, appropriately, refined the questions of who, how, when and at what risk and cost. These are welcome challenges require intensified, cross-disciplinary responses. This is especially true in the areas of adherence and pharmacokinetic/pharmacodynamics (PK/PD) sampling and modeling to optimize preventive trials measuring &quot;efficacy&quot;, which is well known to reduce when measured as &quot;effectiveness&quot; in real-world use. Intensified exploratory and Phase 1 safety trials to investigate acceptability, adherence, PK and ex vivo efficacy with drug-exposed tissue biopsies/compartment fluids even though they are complex in design, management, assays and monitoring are moving forwa...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626536</comments>
            <pubDate>Mon, 16 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626536</guid>        </item>
        <item>
            <title>HIV Microbicides: Where Are We Now?</title>
            <link>http://www.medworm.com/index.php?rid=5626550&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264039%26dopt%3DAbstract</link>
            <description>Authors: Quiñones-Mateu ME, Vanham G
    PMID: 22264039 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626550</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626550</guid>        </item>
        <item>
            <title>Mucosal Transmission of Human Immunodeficiency Virus.</title>
            <link>http://www.medworm.com/index.php?rid=5626549&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264040%26dopt%3DAbstract</link>
            <description>Authors: Tebit DM, Ndembi N, Weinberg A, Quiñones-Mateu ME
    Abstract
    Since the beginning of the AIDS pandemic, and following the discovery of the human immunodeficiency virus (HIV) as the etiological agent of the disease, it was clear that the virus gains access to the human host predominantly through the mucosal tissue after sexual exposure. As a consequence, the female genital tract (vaginal and cervical), as well as the rectal, penile, and oral mucosae have been extensively studied over the last thirty years towards a better understanding of - and to develop strategies to prevent - sexual HIV transmission. This review seeks to describe the biology of the events leading to HIV infection through the human mucosa and introduce some of the approaches attempted to prevent the sexual ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626549</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626549</guid>        </item>
        <item>
            <title>Non-Specific Microbicide Product Development: Then and Now.</title>
            <link>http://www.medworm.com/index.php?rid=5626548&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264041%26dopt%3DAbstract</link>
            <description>Authors: Romano JW, Robbiani M, Doncel G, Moench T
    Abstract
    Despite the identification of HIV-1 as the etiological agent responsible for AIDS nearly 30 years ago, a sterilizing vaccine capable of preventing transmission of the virus remains elusive. In response to struggles on the vaccine development front, significant effort has been devoted to preventing the transmission of HIV with alternative products, technologies, and strategies. One of the early alternative HIV prevention strategies was microbicides, which are topical products that can be used to prevent sexual transmission of HIV either vaginally or rectally. First generation microbicide products were designed to be simple gel formulations comprised of readily available active agents that were inexpensive and broadly active...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626548</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626548</guid>        </item>
        <item>
            <title>Past, Present, and Future of Entry Inhibitors as HIV Microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626547&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264042%26dopt%3DAbstract</link>
            <description>Authors: Gibson RM, Arts EJ
    Abstract
    Preventing the transmission of human immunodeficiency virus (HIV) is the main goal of numerous studies trying to develop an effective vaccine and microbicide agents. Here we review the use of antiretroviral drugs to inhibit viral entry as potential HIV microbicides. After the failure of nonoxynol-9 microbicide strategies shifted towards the use of compounds creating a physical barrier to virus attachment (e.g., surfactants) or inhibit the virus in the vaginal milieu (e.g., polyanions). These early, non-specific inhibitors showed promise in both in vitro and in vivo(non-human primates) studies but provided only modest protection from HIV transmission in clinical efficacy trials. The next generation of HIV entry microbicides was based on specifica...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626547</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626547</guid>        </item>
        <item>
            <title>Reverse Transcriptase Inhibitors as Microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626546&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264043%26dopt%3DAbstract</link>
            <description>Authors: Lewi P, Heeres J, Ariën K, Venkatraj M, Joossens J, Van der Veken P, Augustyns K, Vanham G
    Abstract
    The CAPRISA 004 study in South Africa has accelerated the development of vaginal and rectal microbicides containing antiretrovirals that target specific enzymes in the reproduction cycle of HIV, especially reverse transcriptase inhibitors (RTI). In this review we discuss the potential relevance of HIV-1 RTIs as microbicides, focusing in the nucleotide RTI tenofovir and six classes of nonnucleoside RTIs (including dapivirine, UC781, urea and thiourea PETTs, DABOs and a pyrimidinedione). Although tenofovir and dapivirine appear to be most advanced in clinical trials as potential microbicides, several issues remain unresolved, e.g., the importance of nonhuman primates as a &quot;ga...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626546</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626546</guid>        </item>
        <item>
            <title>Will Integrase Inhibitors be used as Microbicides?</title>
            <link>http://www.medworm.com/index.php?rid=5626545&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264044%26dopt%3DAbstract</link>
            <description>Authors: Crucittia GC, Botta M, Di Santoa R
    Abstract
    Microbicides are products that can be applied to vaginal or rectal mucosal surfaces with the goal of preventing, or at least significantly reducing, the transmission of sexually transmitted infections including HIV-1. Despite more than two decades of HIV-1 research, there is still no efficacious HIV-1 vaccine, and the scientific community appears sceptical about the short or long-term feasibility of developing a vaccine that has the ability to induce sterilizing immunity against HIV-1. In this setting, microbicide research has been developed. Among the promising candidate microbicides, the integrase inhibitors are the most recently developed compounds. In fact, since the beginning reverse transcriptase, fusion and entry inhibitor...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626545</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626545</guid>        </item>
        <item>
            <title>Potential use of protease inhibitors as vaginal and colorectal microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626544&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264045%26dopt%3DAbstract</link>
            <description>Authors: Herrera C, Shattock RJ
    Abstract
    The new generation of microbicide candidates is based on the use of antiretroviral (ARV) drugs. The first compounds tested were selected among ARV classes that block the early stages of viral replication cycle, either entry/fusion or reverse transcription. Recently, an additional class of ARVs acting on a later step of viral replication has entered the microbicide pipeline, the protease inhibitors (PIs). This class of ARVs has shown strong potency in highly active antiretroviral therapy (HAART) against human immunodeficiency-1 virus (HIV-1) and lower levels of induced resistance compared to other ARV classes. As candidate microbicides, PIs will have to follow the guiding principles of microbicides being effective, safe, user-friendly and aff...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626544</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626544</guid>        </item>
        <item>
            <title>Combination of antiretroviral drugs as microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626543&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264046%26dopt%3DAbstract</link>
            <description>Authors: Balzarini J, Schols D
    Abstract
    Tenofovir, a highly prescribed drug for the treatment of HIV/AIDS infections, has recently also shown its effectiveness as a potential topical microbicide drug in the prevention of HIV transmission. Here, we discuss the combination of tenofovir with variousother antiretrovirals (ARV) highlighting the large class of carbohydrate-binding agents (CBAs) targeting the glycans on the viral envelope gp120 for their anti-HIV activity and their favorable combinatory potential.Thetenofovir/CBA and several other ARV combinations consistently showed synergistic antiviral activities. Also combinations of other classes of ARV such as receptor (i.e. CD4, CXCR4 and CCR5) inhibitors, various monoclonal antibodies (mAbs)directed against the HIV envelope gp120 ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626543</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626543</guid>        </item>
        <item>
            <title>Mechanisms and Modifications of Naturally Occurring Host Defense Peptides for Anti-HIV Microbicide Development.</title>
            <link>http://www.medworm.com/index.php?rid=5626542&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264047%26dopt%3DAbstract</link>
            <description>Authors: Eade CR, Wood MP, Cole AM
    Abstract
    Despite advances in the treatment of HIV infection, heterosexual transmission of HIV remains high, and vaccines to prevent HIV acquisition have been unfruitful. Vaginal microbicides, on the other hand, have demonstrated considerable potential for HIV prevention, and a variety of compounds have been screened for their activity and safety as anti-HIV microbicides. Among these are the naturally occurring host defense peptides, small peptides from diverse lineages with intrinsic antiviral activity. Naturally occurring host defense peptides with anti-HIV activity are promising candidates for vaginal microbicide development. Their structural variance and accompanying mechanistic diversity provide a wide range of inhibitors whose antiviral activ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626542</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626542</guid>        </item>
        <item>
            <title>Ex vivo models of HIV sexual transmission and microbicide development.</title>
            <link>http://www.medworm.com/index.php?rid=5626541&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264048%26dopt%3DAbstract</link>
            <description>Authors: Ariën KK, Kyongo JK, Vanham G
    Abstract
    Here, we review the armamentarium on in vitro/ex vivo models of HIV sexual transmission and discuss how these models can be applied to study candidate microbicide.
    PMID: 22264048 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626541</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626541</guid>        </item>
        <item>
            <title>Animal models for microbicide studies.</title>
            <link>http://www.medworm.com/index.php?rid=5626540&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264049%26dopt%3DAbstract</link>
            <description>Authors: Veazey RS, Shattock RJ, Klasse PJ, Moore JP
    Abstract
    There have been encouraging recent successes in the development of safe and effective topical microbicides to prevent vaginal or rectal HIV-1 transmission, based on the use of anti-retroviral drugs. However, much work remains to be accomplished before a microbicide becomes a standard element of prevention science strategies. Animal models should continue to play an important role in pre-clinical testing, with emphasis on safety, pharmacokinetic and efficacy testing.
    PMID: 22264049 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626540</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626540</guid>        </item>
        <item>
            <title>Formulation and Delivery of Microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626539&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264050%26dopt%3DAbstract</link>
            <description>Authors: Agashe H, Hu M, Rohan L
    Abstract
    The development of pre-exposure prophylactics or microbicide products for the reduction or elimination of the sexual transmission of HIV has numerous challenges or barriers to success. Historically traditional dosage forms such as gels have been developed in the field but more recently controlled release dosage forms such as vaginal rings and novel dosage forms such as polymeric thin films have been studied. Studies have begun to incorporate scientific strategies into the formulation design of microbicide products in order to develop safer and more effective products. In addition advanced drug delivery strategies to overcome barriers to delivery and specific drug targeting methods are being employed. In the present review, a comprehensive d...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626539</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626539</guid>        </item>
        <item>
            <title>An Algorithm for the Preclinical Development of Anti-HIV Topical Microbicides.</title>
            <link>http://www.medworm.com/index.php?rid=5626538&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264051%26dopt%3DAbstract</link>
            <description>Authors: Buckheit Jr RW, Buckheit KW
    Abstract
    Throughout the world, and especially in countries comprising the developing world, women are now bearing the brunt of the HIV pandemic, with over 50% living with HIV infection primarily contracted through sexual transmission in monogamous relationships Thus, effective chemical or physical means of preventing HIV transmission are urgently needed and in the absence of an approved and effective vaccine, microbicides have become the strategy of choice to provide women with the ability to prevent HIV transmission from their infected partners. Topical microbicides include agents specifically developed and formulated for use in either the vaginal or rectal environment to prevent the sexual transmission of infectious organisms, including pathog...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626538</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626538</guid>        </item>
        <item>
            <title>Ethical Issues in Microbicide Clinical Trials for HIV Prevention.</title>
            <link>http://www.medworm.com/index.php?rid=5626537&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22264052%26dopt%3DAbstract</link>
            <description>Authors: Gangestad AK, Salata RA
    Abstract
    Women account for half of new infections with HIV annually. Heterosexual transmission is the most common route of infection in resource limited settings (RLS). An effective microbicide would help decrease transmission of HIV and potentially enable women to have more control in sexual relationships. Research into microbicides is done predominantly in RLS. In addition, there will be different issues and challenges to consider with respect to rectal microbicide use in men. There exist several ethical issues around microbicide development and clinical research which we explore in this review. Respect for persons, including autonomy and protection of vulnerable populations, beneficence, and justice are explored as they relate to microbicide rese...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5626537</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5626537</guid>        </item>
        <item>
            <title>The Influence of AIDS on the Morphometric and Immune Status of the Uterine Cervix of Autopsied Patients.</title>
            <link>http://www.medworm.com/index.php?rid=5568304&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211654%26dopt%3DAbstract</link>
            <description>Conclusion: AIDS causes alterations in the structure of the cervical epithelium and in its extracellular matrix, leading to alterations in the local and systemic immunity, and triggering signs and opportunistic infections in the uterine cervix in the course of the disease.
    PMID: 22211654 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568304</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568304</guid>        </item>
        <item>
            <title>HIV Drug Resistance on HAART Despite an Undetectable Viral Load.</title>
            <link>http://www.medworm.com/index.php?rid=5568303&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211655%26dopt%3DAbstract</link>
            <description>We present the case of an HIV-infected patient who developed mutations of resistance to nevirapine although he always had an undetectable viral load and without context of inobservance. The concepts of undetectability and virological success in HIV infection must be balanced by the possible appearance of resistance under a treatment considered as effective.
    PMID: 22211655 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568303</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568303</guid>        </item>
        <item>
            <title>Position 22 of the V3 Loop is Associated with Co-Receptor Usage and Disease Progression in HIV-1 Subtype B Isolates.</title>
            <link>http://www.medworm.com/index.php?rid=5568302&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211656%26dopt%3DAbstract</link>
            <description>Authors: Zhou HZ, Xu HF, Xin XM, Guan XR, Zhou J
    Abstract
    Our goal in this study was to analyze position 22 of the V3 loop associated with co-receptor usage and disease progression in human immunodeficiency virus type 1 (HIV-1) subtype B infection. Bioinformatics approaches were used to compare the amino acid sequence and secondary structure of the V3 loop of the CCR5-tropic virus and CXCR4-tropic virus in HIV-1 subtype B. HIV-1 subtype B V3 amino acid sequence files in the FASTA format were collected from the HIV Sequence Database. The amino acid sequences of different tropism were multiple-aligned with CLUSTAL W program, and the frequencies of the amino acids at each position of the V3 loop sequences of two groups were calculated and sorted in descending order. The secondary stru...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568302</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568302</guid>        </item>
        <item>
            <title>Application of Outer Membrane Vesicle of Neisseria meningitides Serogroup B as a New Adjuvant to Induce Strongly Th1-Oriented Responses Against HIV-1.</title>
            <link>http://www.medworm.com/index.php?rid=5568299&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211657%26dopt%3DAbstract</link>
            <description>Authors: Aghasadeghi MR, Salmani AS, Sadat SM, Javadi F, Memarnejadian A, Vahabpour R, Zabihollahi R, Moshiri A, Siadat SD
    Abstract
    Despite the worldwide efforts made in the field of HIV vaccine development, an efficient AIDS vaccine strategy is still vague. Virus-like particles (VLPs) are one of the introduced aspects for HIV vaccine development since the non-replicative nature of HIV VLPs, resulted from the lack of viral genomic RNA, makes them suitable for broad applications. We have previously designed and introduced non-infectious VLPs (mzNL4-3) by introduction of a deletion mutation in the reverse transcriptase and integrase coding regions of HV-1. There are evidences suggesting that an effective cellular immune response against HIV-1 is able to control and suppress viremia d...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568299</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568299</guid>        </item>
        <item>
            <title>Induction of Strong Anti-HIV Cellular Immunity by a Combination of Clostridium Perfringens Expressing HIV Gag and Virus Like Particles.</title>
            <link>http://www.medworm.com/index.php?rid=5568295&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211658%26dopt%3DAbstract</link>
            <description>Authors: Pegu P, Helmus R, Gupta P, Tarwater P, Caruso L, Shen C, Ross T, Chen Y
    Abstract
    The lower gastrointestinal tract is a major mucosal site of HIV entry and initial infection. Thus, the induction of strong cellular immune responses at this mucosal site will be an important feature of an effective HIV vaccine. We have used a novel prime-boost vaccination approach to induce immune responses at mucosal sites. Orally delivered recombinant Clostridium perfringens expressing HIV-1 gag (Cp-Gag) was evaluated for induction of HIV-1 Gag specific T cell responses in a prime-boost model with intranasal inoculation of HIV-1 virus like particles (VLP). HIV-1 specific cellular immune responses in both the effector (Lamina propria) and inductive sites (Peyer's patches) of the gastrointesti...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568295</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568295</guid>        </item>
        <item>
            <title>Does GSS Still Maintain Relevance on HAART Outcome After the Introduction of Newest Active Antiretroviral Drugs? 48 Weeks Results.</title>
            <link>http://www.medworm.com/index.php?rid=5568293&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211659%26dopt%3DAbstract</link>
            <description>Conclusions: Single drugs belonging to new antiretroviral classes did not correlate to viroimmunological success for any GSS. High frequency and recurrence over GRTs for specific mutations confirms their key role following the exposure to ARVs classes. A baseline HIV-RNA &amp;lt;50,000 cp/ml is a predictor of therapeutic success and a carefully selected HAART based upon the evaluation of GRTs can favorably influence the immunovirologic response.
    PMID: 22211659 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568293</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568293</guid>        </item>
        <item>
            <title>Control of HIV latency by epigenetic and non-epigenetic mechanisms.</title>
            <link>http://www.medworm.com/index.php?rid=5568292&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211660%26dopt%3DAbstract</link>
            <description>Authors: Mbonye U, Karn J
    Abstract
    Intensive antiretroviral therapy successfully suppresses viral replication but is unable to eradicate the virus. HIV persists in a small number of resting memory T-cells where HIV has been transcriptionally silenced. This review will focus on recent insights into the HIV transcriptional control mechanisms that provide the biochemical basis for understanding latency. There are no specific repressors of HIV transcription encoded by the virus, instead latency arises when the regulatory feedback mechanism driven by HIV Tat expression is disrupted. Small changes in transcriptional initiation, induced by epigenetic silencing, lead to profound restrictions in Tat levels and force the entry of proviruses into latency. In resting memory T-cells, which carr...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568292</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568292</guid>        </item>
        <item>
            <title>Facts and Fiction: Cellular Models for High Throughput Screening for HIV-1 Reactivating Drugs.</title>
            <link>http://www.medworm.com/index.php?rid=5568291&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211661%26dopt%3DAbstract</link>
            <description>Authors: Planelles V, Wolschendorf F, Kutsch O
    Abstract
    A curative therapy for HIV-1 infection will have to include measures to eliminate the reservoir of latently HIV-1 infected cells that allow the virus to persist despite otherwise successful therapy. To date, all efforts to deplete the latent reservoir by triggering viral reactivation have used preexisting drugs that are believed to potentially target molecular mechanisms controlling HIV-1 infection. These therapeutic attempts were not clinically successful. Only in the last few years have cellular models of latent HIV-1 infection suitable for high throughput screening been developed and concerted drug discovery effortswere initiated to discover new HIV-1 reactivating drugs. We here providea historic overview about the developm...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568291</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568291</guid>        </item>
        <item>
            <title>Models of HIV-1 Persistence in the CD4+ T Cell Compartment: Past, Present and Future.</title>
            <link>http://www.medworm.com/index.php?rid=5568290&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211662%26dopt%3DAbstract</link>
            <description>Authors: Tyagi M, Romerio F
    Abstract
    The limitations of current anti-retroviral therapies (ART) and the lack of a valid anti-HIV-1 vaccine candidate underscore the need for new therapeutic concepts aiming at the eradication of HIV-1, which represents at the same time an ideal goal and a major challenge for AIDS research. At present, this aim is unattainable due to the existence of cellular and anatomical reservoirs of persistent infection. Memory CD4+ T cells comprise the largest pool of cells harboring silent, stably integrated HIV-1, which remains undetected by the immune system and refractory to conventional anti-retroviral drugs. The eradication of latent HIV-1 reservoirs will require new, potent and specific therapeutic strategies, which in turn must rely upon a deeper underst...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568290</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568290</guid>        </item>
        <item>
            <title>Implications of RNA Helicases in HIV-1 replication: Possible roles in latency.</title>
            <link>http://www.medworm.com/index.php?rid=5568284&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211663%26dopt%3DAbstract</link>
            <description>Authors: Ajamian L, Mouland AJ
    Abstract
    HAART treatment has greatly improved life expectancy of HIV-1-infected individuals. Unfortunately, latency still remains the major barrier towards HIV-1 eradication. Efforts to identify viral and host cell proteins involved in latency remain important research areas to win this war against HIV-1. Here, we review the contributions of several factors in the establishment of latently infected cells. In addition, we also raise the possibility that RNA helicases, while playing important roles at almost every step of the HIV-1 replication cycle, could be implicated in the processes governing the establishment of these latent reservoirs.
    PMID: 22211663 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568284</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568284</guid>        </item>
        <item>
            <title>Humanized mouse models of HIV-1 latency.</title>
            <link>http://www.medworm.com/index.php?rid=5568254&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22211664%26dopt%3DAbstract</link>
            <description>Authors: Duyne RV, Narayanan A, Kehn-Hall K, Saifuddin M, Shultz L, Kashanchi F
    Abstract
    The existence of long-lasting cellular reservoirs of HIV-1 is one of the major hurdles in developing effective anti-retroviral therapies. These latently infected cells and tissues efficiently evade immune responses and remain dormant until activated, upon which they can generate a productive HIV-1 infection. This classic scenario of viral latency becomes even more difficult to study and model due to the extreme complexity of translating in vivo virus-cell interactions into a controlled in vitro system. The recent developments and constant improvements upon hematopoietic engraftment of human cells and tissues onto recipient immunocompromised murine scaffolds have made it possible to model comple...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5568254</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5568254</guid>        </item>
        <item>
            <title>The nef-infectivity enigma: mechanisms of enhanced lentiviral infection.</title>
            <link>http://www.medworm.com/index.php?rid=5446538&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103831%26dopt%3DAbstract</link>
            <description>THE NEF-INFECTIVITY ENIGMA: MECHANISMS OF ENHANCED LENTIVIRAL INFECTION.
    Curr HIV Res. 2011 Nov 18;
    Authors: Vermeire J, Vanbillemont G, Witkowski W, Verhasselt B
    Abstract
    The Nef protein is an essential factor for lentiviral pathogenesis in humans and other simians. Despite a multitude of functions attributed to this protein, the exact role of Nef in disease progression remains unclear. One of its most intriguing functions is the ability of Nef to enhance the infectivity of viral particles. In this review we will discuss current insights in the mechanism of this well-known, yet poorly understood Nef effect. We will elaborate on effects of Nef, on both virion biogenesis and the early stage of the cellular infection, that might be involved in infectivity enhancement. In addi...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446538</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446538</guid>        </item>
        <item>
            <title>Role of the cd4 down-modulation activity of nef in hiv-1 infectivity.</title>
            <link>http://www.medworm.com/index.php?rid=5446537&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103832%26dopt%3DAbstract</link>
            <description>ROLE OF THE CD4 DOWN-MODULATION ACTIVITY OF NEF IN HIV-1 INFECTIVITY.
    Curr HIV Res. 2011 Nov 18;
    Authors: Doria M
    Abstract
    The regulatory Nef protein of HIV-1/2 and SIV is required for high viral replication and disease progression, thus represents a very attractive therapeutic target. Because of the multi-functional nature of the Nef protein, it is unclear which of the several Nef activities are most crucial in vivo for the outcome of viral infection. Some findings indicate that the CD4 down-regulation activity of Nef is critical for viral infectivity as well as for progression to immunodeficiency. On the other hand, more recent evidences suggest that CD4 targeting and stimulation of infectivity are two separate functions of Nef. This controversial issue will be discussed ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446537</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446537</guid>        </item>
        <item>
            <title>One protein to rule them all: modulation of cell surface receptors and molecules by hiv nef.</title>
            <link>http://www.medworm.com/index.php?rid=5446536&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103833%26dopt%3DAbstract</link>
            <description>ONE PROTEIN TO RULE THEM ALL: MODULATION OF CELL SURFACE RECEPTORS AND MOLECULES BY HIV NEF.
    Curr HIV Res. 2011 Nov 18;
    Authors: Landi A, Iannucci V, Nuffel AV, Meuwissen P, Verhasselt B
    Abstract
    The HIV-1, HIV-2 and SIV Nef protein is known to modulate the expression of several cell surface receptors and molecules to escape the immune system, to alter T cell activation, to enhance viral replication, infectivity and transmission and overall to ensure the optimal environment for the outcome of infection. Consistent and continuous efforts have been made during the years to characterize the down-regulation of each of these molecules, in the hope that a better understanding of these processes essential for HIV infection and/or pathogenesis will eventually highlight new therapeu...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446536</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446536</guid>        </item>
        <item>
            <title>Nef performance in Macrophages: the Master Orchestrator of Viral Persistence and Spread.</title>
            <link>http://www.medworm.com/index.php?rid=5446535&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103834%26dopt%3DAbstract</link>
            <description>Authors: Ghiglione Y, Turk G
    Abstract
    Following transmission of human immunodeficiency virus (HIV) into a new host, cells of the monocyte/macrophage lineage play a central role in host invasion and viral replication. In particular, macrophages survive infection and support long-standing viral replication, contributing to viral persistence within the host and representing a viral reservoir in vivo. On the other hand, HIV Nef protein is a small though versatile molecule that plays an unquestioned key role in viral pathogenesis. In macrophages, Nef is able to modulate cell surface receptor expression, to intersect intracellular signaling pathways and to augment the release of pro-inflammatory and chemotactic molecules. In addition, Nef can alter macrophage phagocytic capacity, autopha...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446535</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446535</guid>        </item>
        <item>
            <title>Tetherin Antagonism by Primate Lentiviral Nef Proteins.</title>
            <link>http://www.medworm.com/index.php?rid=5446534&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103835%26dopt%3DAbstract</link>
            <description>Authors: Sauter D, Kirchhoff F
    Abstract
    The multifunctional Nef protein of primate lentiviruses is commonly considered an early viral factor that down-modulates various receptors from the cell surface and modulates several signaling pathways to facilitate viral immune evasion and to render the cell conducive for viral replication. However, Nef also acts during the late stages of infection, e.g. by increasing the infectivity of progeny virions. Just recently, it has become clear that many primate lentiviruses that have been detected in about 40 different monkey and ape species also use Nef to antagonize tetherin (BST2/CD317), a cellular factor that inhibits virus release by tethering nascent viral particles to the cell surface. Exceptions are some simian immunodeficiency viruses (SI...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446534</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446534</guid>        </item>
        <item>
            <title>The CD4C/HIVNef Transgenic Model Of Aids.</title>
            <link>http://www.medworm.com/index.php?rid=5446533&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103836%26dopt%3DAbstract</link>
            <description>Authors: Jolicoeur P
    Abstract
    CD4C/HIVNef Tg mice express HIV-1 Nef in relevant target cells through the regulatory sequences of the human CD4 gene. These mice develop a severe disease showing many characteristics of human AIDS. A summary of the results obtained with these Tg mice is presented.
    PMID: 22103836 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446533</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446533</guid>        </item>
        <item>
            <title>Interactions of the HIV/SIV Pathogenicity Factor Nef with SH3 Domain-Containing Host Cell Proteins.</title>
            <link>http://www.medworm.com/index.php?rid=5446532&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103837%26dopt%3DAbstract</link>
            <description>Authors: Saksela K
    Abstract
    A bewildering number of host cell proteins associated with Nef can be found in the literature and in the public protein interaction databases. However, only in a few of these cases, including binding of Nef to certain Src homology-3 (SH3) domain proteins, is the interaction understood in any molecular detail or even known to be direct. Indeed, SH3 binding capacity by Nef is required for many of the other protein interactions to take place, suggesting that a large proportion of the latter is indirectly coupled to Nef via an SH3 protein. Accordingly, the proline-rich SH3 binding site, the &quot;PxxP motif&quot;, is one of the key functional determinants of Nef. It is highly conserved among the lentiviral Nef proteins, and mutations disrupting it abrogate the majorit...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446532</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446532</guid>        </item>
        <item>
            <title>Nef Surfaces: Where to Interfere with Function.</title>
            <link>http://www.medworm.com/index.php?rid=5446531&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22103838%26dopt%3DAbstract</link>
            <description>Authors: Lülf S, Horenkamp FA, Breuer S, Geyer M
    Abstract
    The HIV-1 Nef protein is an accessory protein of 24-27 kDa mass that mediates a multitude of effector functions in infected cells. Although not essentially required for viral replication, HIV-1 Nef exhibits stimulating potential towards disease progression to AIDS and is therefore considered a pathogenic factor in retroviridae. Here we correlate sequence conservation in HIV-1 Nef with surface hydrophobicity and functionality in protein-protein interaction to identify accessible substructures on the surface of Nef that might be suitable as pharmacological target sites. Recent advances in targeting of Nef by small molecular compounds that interfere with SH3 domain binding or MHC class I down-regulation are discussed. Similarl...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5446531</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5446531</guid>        </item>
        <item>
            <title>Harnessing the Prevention Benefits of Antiretroviral Treatment to Address HIV and Tuberculosis.</title>
            <link>http://www.medworm.com/index.php?rid=5332601&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999771%26dopt%3DAbstract</link>
            <description>Authors: Granich R, Lo YR, Suthar A, Vitoria M, Baggaley R, Mahklouf-Obermeyer C, McClure C, Souteyrand Y, Perriens J, Kahn JG, Bennett R, Smyth C, Williams B, Montaner J, Hirnschall G
    Abstract
    After 30 years we are still struggling to address a devastating HIV pandemic in which over 25 million people have died. In 2010, an estimated 34 million people were living with HIV, around 70% of these in sub-Saharan Africa. Furthermore, in 2009 there were an estimated 1.2 million new HIV-associated TB cases, and TB accounted for 24% of HIV-related deaths. By the end of 2010, 6.6 million people were taking antiretroviral therapy (ART), around 42% of those in need as defined by the 2010 World Health Organization (WHO). Despite this achievement, around 9 million people were eligible and still ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332601</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332601</guid>        </item>
        <item>
            <title>Modelling the Impact of Antiretroviral Therapy on the Epidemic of HIV.</title>
            <link>http://www.medworm.com/index.php?rid=5332600&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999772%26dopt%3DAbstract</link>
            <description>Authors: Williams B, Lima V, Gouws E
    Abstract
    Thirty years after HIV first appeared it has killed close to 30 million people but transmission continues unchecked. In 2009, an estimated 1.8 million lives were lost and 2.6 million more people were infected with HIV [1]. To cut transmission, many social, behavioural and biomedical interventions have been developed, tested and tried but have had little impact on the epidemic in most countries. One substantial success has been the development of combination antiretroviral therapy (ART) that reduces viral load and restores immune function. This raises the possibility of using ART not only to treat people but also to prevent new HIV infections. Here we consider the impact of ART on the transmission of HIV and show how it could help to con...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332600</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332600</guid>        </item>
        <item>
            <title>Antiretroviral Treatment as Prevention: Impact of the 'Test and Treat' Strategy on the Tuberculosis Epidemic.</title>
            <link>http://www.medworm.com/index.php?rid=5332599&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999773%26dopt%3DAbstract</link>
            <description>Authors: Wood R, Lawn SD
    Abstract
    Antiretroviral therapy (ART) has been remarkably effective in ameliorating Human Immunodeficiency Virus (HIV)-associated morbidity and mortality. The rapid decline in viral load during ART also presents an opportunity to develop a &quot;treatment as prevention&quot; strategy in order to reduce HIV transmission at a population level. Modelling exercises have demonstrated that for this strategy to be effective, early initiation of ART with high coverage of the HIVinfected population will be required. The HIV epidemic has fueled a resurgence of tuberculosis (TB) particularly in sub- Saharan Africa and widespread early initiation of ART could also impact this epidemic via several mechanisms. The proportion of patients with low CD4 cell counts who are at high ris...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332599</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332599</guid>        </item>
        <item>
            <title>The Unrealized Potential of Addiction Science in Curbing the HIV Epidemic.</title>
            <link>http://www.medworm.com/index.php?rid=5332598&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999774%26dopt%3DAbstract</link>
            <description>Authors: Volkow ND, Baler RD, Normand JL
    Abstract
    The stubbornly high incidence of new HIV infections belies the overwhelming evidence showing that sustained highly active antiretroviral therapy (HAART) has the power to dramatically reduce the spread of HIV infection and forever change the face of this devastating epidemic. One of the main contributors to this public health paradox is the ongoing HIV epidemic among substance users who contribute significantly to HIV infection rates through injection drug use and high-risk sexual behaviours. Current evidence clearly shows that, in order to fill this gap, we need to integrate substance abuse treatment with HIV treatment programmes and provide substance abusers with universal access to HIV treatment through a focussed effort to seek, ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332598</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332598</guid>        </item>
        <item>
            <title>Articulating A Rights-Based Approach to HIV Treatment and Prevention Interventions.</title>
            <link>http://www.medworm.com/index.php?rid=5332597&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999775%26dopt%3DAbstract</link>
            <description>Authors: Barr D, Amon JJ, Clayton M
    Abstract
    Since the beginning of the epidemic, the protection of human rights has been an integral component in the response to Human Immunodeficiency Virus (HIV). The high degree of stigma and discrimination associated with acquired immune deficiency syndrome (AIDS) has made human rights protection not only a priority to ensure the rights of people living with and at-risk for HIV, but to address public health goals as well. Advances in understanding the impact of antiretroviral treatment on HIV prevention provide exciting opportunities and even a paradigm shift in terms of AIDS prevention. However, this potential cannot be reached unless the advancement of human rights is a primary component of treatment and prevention programme and policy develo...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332597</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332597</guid>        </item>
        <item>
            <title>Cost-Effectiveness of Antiretroviral Therapy for Prevention.</title>
            <link>http://www.medworm.com/index.php?rid=5332596&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999776%26dopt%3DAbstract</link>
            <description>We describe critical issues in the epidemic impact of ART, such as suppression of transmission and the role of the acute phase of infection. We then present a conceptual model for conducting and interpreting cost-effectiveness analyses of ART as prevention, and review the existing preliminary estimates in this area. We end with a discussion of future directions for programmatic demonstrations and evaluation.
    PMID: 21999776 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332596</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332596</guid>        </item>
        <item>
            <title>Costing Human Rights and Community Support Interventions as a Part of Universal Access to HIV Treatment and Care in a Southern African Setting.</title>
            <link>http://www.medworm.com/index.php?rid=5332595&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999777%26dopt%3DAbstract</link>
            <description>Authors: Jones L, Akugizibwe P, Clayton M, Amon JJ, Sabin M, Bennett R, Stegling C, Baggaley R, Kahn JG, Holmes CB, Garg N, Makhlouf-Obermeyer C, Defilippo Mack C, Williams P, Smyth C, Vitoria M, Crowley S, Williams B, McClure C, Granich R, Hirnschall G
    Abstract
    Expanding access to antiretroviral therapy (ART) has both individual health benefits and potential to decrease HIV incidence. Ensuring access to HIV services is a significant human rights issue and successful programmes require adequate human rights protections and community support. However, the cost of specific human rights and community support interventions for equitable, sustainable and non-discriminatory access to ART are not well described. Human rights and community support interventions were identified using the li...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332595</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332595</guid>        </item>
        <item>
            <title>Universal Testing and Treatment as an HIV Prevention Strategy: Research Questions and Methods.</title>
            <link>http://www.medworm.com/index.php?rid=5332594&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999778%26dopt%3DAbstract</link>
            <description>Authors: Hayes R, Sabapathy K, Fidler S
    Abstract
    Achieving high coverage of antiretroviral treatment (ART) in resource-poor settings will become increasingly difficult unless HIV incidence can be reduced substantially. Universal voluntary counselling and testing followed by immediate initiation of ART for all those diagnosed HIV-positive (universal testing and treatment, UTT) has the potential to reduce HIV incidence dramatically but would be very challenging and costly to deliver in the short term. Early modelling work in this field has been criticised for making unduly optimistic assumptions about the uptake and coverage of interventions. In future work, it is important that model parameters are realistic and based where possible on empirical data. Rigorous research evidence is n...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332594</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332594</guid>        </item>
        <item>
            <title>Antiretrovirals therapy in Prevention of HIV and TB: Update on Current Research Efforts.</title>
            <link>http://www.medworm.com/index.php?rid=5332593&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999779%26dopt%3DAbstract</link>
            <description>Authors: Granich R, Gupta S, Suthar AB, Smyth C, Hoos D, Vitoria M, Bavicchi Simao M, Hankins C, Schwartlander B, Ridzon R, Bazin B, Williams B, Lo YR, McClure C, Montaner J, Hirnschall G, 
    Abstract
    There is considerable scientific evidence supporting the use of antiretroviral therapy (ART) in prevention of human immunodeficiency virus (HIV) and tuberculosis (TB) infections. The complex nature of the HIV and TB prevention responses, resource constraints, remaining questions about cost and feasibility, and the need to use a solid evidence base to make policy decisions, and the implementation challenges to translating trial data to operational settings require a well-organised and coordinated response to research in this area. To this end, we aimed to catalogue the ongoing and planne...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332593</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332593</guid>        </item>
        <item>
            <title>Antiretrovirals for Prevention: Realizing the Potential. Closing Commentary by the Executive Director of UNAIDS.</title>
            <link>http://www.medworm.com/index.php?rid=5332592&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999780%26dopt%3DAbstract</link>
            <description>Authors: Sidibé M
    Abstract
    Antiretroviral therapy (ART), for those who have access, has revolutionised the morbidity and mortality consequences of HIV infection. By the end of 2010, 6.6 million people living with HIV in low- and middle-income countries were receiving ART, a dramatic 20-fold increase since 2001, saving millions of lives. In addition to the impact of ART on the health of those living with HIV, recent randomised controlled trials demonstrate the additional impact of ART in reducing HIV transmission. With this double effect, ART can be a game changer in the response to AIDS. Science has seen dramatic advances over the past year. We have a set of effective tools to stop the transmission of the virus and to keep people living with HIV healthy and productive. It is now t...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332592</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332592</guid>        </item>
        <item>
            <title>Itraconazole vs Fluconazole as a Primary Prophylaxis for Fungal Infections in HIV-Infected Patients in Thailand.</title>
            <link>http://www.medworm.com/index.php?rid=5234963&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21916838%26dopt%3DAbstract</link>
            <description>Conclusions: Although P. marneffei has a reduced susceptibility in in vitro to fluconazole, our study has demonstrated that once-weekly fluconazole is at least as effective as once-daily itraconazole as primary prophylaxis for systemic fungal infections in AIDS patients in northern Thailand.
    PMID: 21916838 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5234963</comments>
            <pubDate>Thu, 15 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5234963</guid>        </item>
        <item>
            <title>HIV Shedding in Cervico-Vaginal Secretions in Pregnant Women.</title>
            <link>http://www.medworm.com/index.php?rid=5234962&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21916839%26dopt%3DAbstract</link>
            <description>Conclusion: The shedding of genital HIV was increased in pregnant compared to non pregnant subjects, even in patients with undetectable viremia. In this low-risk HIV-positive population the risks of vertical or horizontal transmissions should not be underestimated.
    PMID: 21916839 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5234962</comments>
            <pubDate>Thu, 15 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5234962</guid>        </item>
        <item>
            <title>HIV Infection-Related Premature Immunosenescence: High Rates of Immune Exhaustion After Short Time of Infection.</title>
            <link>http://www.medworm.com/index.php?rid=5234961&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21916840%26dopt%3DAbstract</link>
            <description>Authors: Ferrando-Martínez S, Ruiz-Mateos E, Romero-Sánchez MC, Muñoz-Fernández MA, Viciana PP, Genebat M, Leal M
    Abstract
    Premature immunosenescence has been reported in different HIV scenarios. However, how premature is the HIV-related immunosenescent phenotype is still unknown. Thus, the aim of this study was to analyze the immunosenescent status of young viraemic naive HIV-infected individuals, with less than four years from infection. To this end, replicative senescence, activation and proliferation T-cell levels were analyzed in chronically HIV-infected young individuals and both, elderly and young healthy controls. We show that young HIV-infected viraemic patients, with less than four years from infection, have early immune exhaustion leading to a premature immunosenesce...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5234961</comments>
            <pubDate>Thu, 15 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5234961</guid>        </item>
        <item>
            <title>Investigation of Structure-Activity Relationship Between Chemical Structure and CCR5 Anti HIV-1 Activity in a Class of 1-[N-(Methyl)-N- (Phenylsulfonyl)Amino]-2-(Phenyl)-4-[4-(Substituted)Piperidin-1-yl]Butane Derivatives: The Electronic-Topological Approach.</title>
            <link>http://www.medworm.com/index.php?rid=5234960&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21916841%26dopt%3DAbstract</link>
            <description>Authors: Saracoglu M, Kandemirli SG, Ba Aran MA, Sayiner H, Kandemirli F
    Abstract
    The relationship between chemical structure and CCR5 anti HIV-1 activity was investigated in the series of 1-[N-(Methyl)-N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted) piperidin-1-yl]butanes derivatives including 114 molecules by using the Electron-Topological Method (ETM). In the frameworks of this approach, its input data were taken as the results of conformational and quantum-mechanical calculations. Conformational analysis and quantumchemical calculations were carried out for each molecule. Then molecular fragments being specific for active molecules and non-active molecules were revealed by using ETM. The result of testing showed the high ability of ETM in predicting the activity and inac...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5234960</comments>
            <pubDate>Thu, 15 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5234960</guid>        </item>
        <item>
            <title>Differential Innate Immune Responses to Low or High Dose Oral SIV Challenge in Rhesus Macaques.</title>
            <link>http://www.medworm.com/index.php?rid=5160344&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21861823%26dopt%3DAbstract</link>
            <description>Authors: Durudas A, Chen HL, Gasper MA, Sundaravaradan V, Milush JM, Silvestri G, Johnson W, Giavedoni LD, Sodora DL
    Abstract
    Mucosal transmission of HIV predominately occurs during sexual intercourse or breast-feeding and generally results in a successful infection from just one or few founder virions. Here we assessed the impact of viral inoculum size on both viral and immune events within two groups of Rhesus macaques that were non-traumatically, orally inoculated with either multiple low (1000 to 4000 TCID(50)) or high (100,000 TCID(50)) doses of SIV. In agreement with previous studies, more diverse SIV variants were observed in macaques following infection with high dose oral SIV compared to a low dose challenge. In peripheral blood cells, the immune gene transcript levels of ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5160344</comments>
            <pubDate>Tue, 23 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5160344</guid>        </item>
        <item>
            <title>The Vpr Gene Polymorphism of Human Immunodeficiency Virus Type 1 in China and its Clinical Significance.</title>
            <link>http://www.medworm.com/index.php?rid=5142750&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827382%26dopt%3DAbstract</link>
            <description>In this study we investigated such relationship in analyzing the Vpr genes of HIV-1 viruses isolated from 208 HIV-1 infected patients from different regions in China. Reverse transcription polymerase chain reaction (RT-PCR) and nested PCR were used to amplify HIV-1 Vpr gene extracted from plasma of 208 HIV-1 infected patients and 153 isolates displayed the target gene sequences. Biological analysis software analyzed the deduced amino acid sequence, and identified the characteristics of the polymorphism of HIV-1 Vpr gene and its clinical significance. Results show the sequence subtypes as follows: CRF01-AE is 51.63%, subtype C is 24.84%, subtype B is 17.65%, CRF03-AB is 3.92% and CRF08-BC is 1.31%.This paper revealed for the first time the HIV-1 Vpr gene polymorphism in HIV-1 positive indiv...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142750</comments>
            <pubDate>Mon, 08 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142750</guid>        </item>
        <item>
            <title>Gender Differences in liver Fibrosis and Hepatitis C Virus-related Parameters in Patients Coinfected with Human Immunodeficiency Virus.</title>
            <link>http://www.medworm.com/index.php?rid=5142749&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827383%26dopt%3DAbstract</link>
            <description>Conclusions: HIV-HCV-coinfected women have more favorable HCV virological and clinical profile than men and, particularly, lower degrees of fibrosis. Alcohol abuse seemed to result more deleterious in women than in men. The reportedly poorer outcomes of liver disease in HIV-HCV-coinfected patients, as compared with their HCV-monoinfected counterparts, could be ameliorated by addressing these cofactors, some of them preventable or treatable.
    PMID: 21827383 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142749</comments>
            <pubDate>Mon, 08 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142749</guid>        </item>
        <item>
            <title>Accuracy of Ultrasound Imaging Technique for Assessing Lipoatrophy in HIV-Infected Subjects.</title>
            <link>http://www.medworm.com/index.php?rid=5142748&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827384%26dopt%3DAbstract</link>
            <description>Conclusions. The results of our study show that in the assessment of subtle subcutaneous fat changes ultrasound is more accurate than clinical evaluation and confirm the usefulness of ultrasound imaging technique in identifying lipoatrophy at an early stage.
    PMID: 21827384 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142748</comments>
            <pubDate>Mon, 08 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142748</guid>        </item>
        <item>
            <title>Lipodystrophy, Insulin Resistance, and Adiponectin Concentration in HIV-Infected Children and Adolescents.</title>
            <link>http://www.medworm.com/index.php?rid=5142747&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827385%26dopt%3DAbstract</link>
            <description>Authors: Viganò A, Zuccotti GV, Cerini C, Stucchi S, Puzzovio M, Giacomet V, Mora S
    Abstract
    Alterations of fat distribution and insulin resistance are associated with increased risk of metabolic derangements and cardiovascular disease. HIV-infected adult patients on antiretroviral treatment often show lipodystrophy, insulin resistance and hypoadiponectinemia, but data in children are controversial. We investigated serum adiponectin concentration in a cohort of HIV-infected youths, and we assessed the relationships with lipodystrophy and insulin resistance. We studied 36 HIV-infected patients (aged 5.0 - 19.4 years), and 171 healthy subjects (aged 4.9 - 17.9 years) for adiponectin measurements. All patients underwent body composition assessment by dual-energy x-ray absorptiometry,...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142747</comments>
            <pubDate>Mon, 08 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142747</guid>        </item>
        <item>
            <title>Women's desire for children in an HIV population. A clinical pilot study in Burkina Faso.</title>
            <link>http://www.medworm.com/index.php?rid=5142746&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827386%26dopt%3DAbstract</link>
            <description>Conclusion: Even if the results of this pilot study are preliminary, they show that HIV positive and negative women have a relatively similar desire for children, even though seropositive women seem to want fewer children than their uninfected counterparts. Most of the reasons which reduce HIV positive women's desire to have children are directly linked to HIV. This is why getting these women informed about materno-fetal transmission risks and existing treatments is really important to give them the opportunity to make a conscious choice.
    PMID: 21827386 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5142746</comments>
            <pubDate>Mon, 08 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5142746</guid>        </item>
        <item>
            <title>Estimated Liver Fibrosis and its Impact on All-Cause Mortality of HCV-Monoinfected and HCV/HIV-Coinfected Drug Users.</title>
            <link>http://www.medworm.com/index.php?rid=4971398&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21675942%26dopt%3DAbstract</link>
            <description>Conclusions: Estimation of liver fibrosis using serum markers may help with clinical decisions to facilitate access to treatment of chronic hepatitis C in this population.
    PMID: 21675942 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971398</comments>
            <pubDate>Tue, 14 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971398</guid>        </item>
        <item>
            <title>The Therapeutic Potential of Adenosine Triphosphate as an Immune Modulator in the Treatment of HIV/AIDS: A Combination Approach with HAART.</title>
            <link>http://www.medworm.com/index.php?rid=4971373&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21675943%26dopt%3DAbstract</link>
            <description>This article presents a strategy for using ATP therapeutically along with background evidence to substantiate the importance of using ATP in the treatment of HIV infection.
    PMID: 21675943 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971373</comments>
            <pubDate>Tue, 14 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971373</guid>        </item>
        <item>
            <title>Detection of Hepatitis B Virus Variants in HBV Monoinfected and HBV/HIV Coinfected Iranian Patients under Lamivudine Treatment.</title>
            <link>http://www.medworm.com/index.php?rid=4971421&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21671883%26dopt%3DAbstract</link>
            <description>Authors: Aghasadeghi MR, Bahramali G, Sadat SM, Farahani A, Mohraz M, Davar Siadat S, Mostafavi E, Memarnejadian A, Ardestani MS, Vahabpour R, Saraji AA, Delbaz SA
    
    PMID: 21671883 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971421</comments>
            <pubDate>Mon, 13 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971421</guid>        </item>
        <item>
            <title>Effects of Tipranavir, Darunavir, and Ritonavir on Platelet Function, Coagulation, and Fibrinolysis in Healthy Volunteers.</title>
            <link>http://www.medworm.com/index.php?rid=4971408&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21671884%26dopt%3DAbstract</link>
            <description>Authors: Kort JJ, Aslanyan S, Scherer J, Sabo JP, Kohlbrenner V, Robinson P
    The use of HIV protease inhibitors (PIs) as part of antiretroviral therapy in the treatment of HIV-1 infection may be associated with an increased risk of bleeding. This prospective, randomized, open-label trial in healthy volunteers compared the effects of tipranavir/ritonavir (TPV/r), darunavir/ ritonavir (DRV/r), and ritonavir (RTV) alone on platelet aggregation after a single dose and at steady-state concentrations. Subjects were selected on the basis of normal platelet aggregation and arachidonic acid (AA)-induced platelet aggregation inhibition after administration of a single 325-mg dose of aspirin. All 3 PI therapies were administered twice daily for 10 days. In some but not all subjects, TPV/r inhibite...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971408</comments>
            <pubDate>Mon, 13 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971408</guid>        </item>
        <item>
            <title>Evaluation of Saliva as an Alternative Matrix for Monitoring Plasma Zidovudine, Lamivudine and Nevirapine Concentrations in Rwanda.</title>
            <link>http://www.medworm.com/index.php?rid=4971407&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21671885%26dopt%3DAbstract</link>
            <description>Authors: Gras A, Schneider S, Karasi JC, Ternes AM, Sauvageot N, Karasi-Omes C, Henry AP, Schmit JC, Seguin-Devaux C, Arendt V
    Saliva may provide interesting advantages as matrix for compliance measurements, pharmacokinetic studies and therapeutic drug monitoring in resource limited countries. We investigated the feasibility of using saliva for compliance monitoring of zidovudine (ZDV), lamivudine (3TC) and nevirapine (NVP) in 29 HIV-1 infected patients from Rwanda. ZDV, 3TC and NVP drug levels were quantified by an LC/MS-MS method in plasma and stimulated saliva samples and compared using Bland-Altman analysis. Seven patients demonstrated undetectable saliva ZDV levels while five out of these seven also showed no 3TC salivary concentrations. For the other samples, we observed a good a...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4971407</comments>
            <pubDate>Mon, 13 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4971407</guid>        </item>
        <item>
            <title>Long-term Medication Adherence in Patients Receiving Antiretroviral Drug Therapy.</title>
            <link>http://www.medworm.com/index.php?rid=4922803&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631425%26dopt%3DAbstract</link>
            <description>Conclusions: This novel approach demonstrates that a proactive method for addressing barriers to long-term medication adherence yields improved patient understanding and preservation of treatment regimens.
    PMID: 21631425 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4922803</comments>
            <pubDate>Wed, 01 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4922803</guid>        </item>
        <item>
            <title>Vertebral Lesions from AIDS-Related Kaposi's Sarcoma.</title>
            <link>http://www.medworm.com/index.php?rid=4922802&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631426%26dopt%3DAbstract</link>
            <description>Conclusion: Vertebral Kaposi's sarcoma is a rare diagnosis but can be accurately diagnosed with CT or MRI imaging in conjunction with a histological diagnosis. An immunosuppressed patient presenting with bone pain should be thoroughly investigated for Kaposi's sarcoma as modern chemotherapeutic agents alongside anti-retroviral therapy may delay or prevent further devastating complications such as spinal cord compression.
    PMID: 21631426 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4922802</comments>
            <pubDate>Wed, 01 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4922802</guid>        </item>
        <item>
            <title>The Burden of Metabolic Diseases Amongst HIV Positive Patients on HAART Attending The Johannesburg Hospital.</title>
            <link>http://www.medworm.com/index.php?rid=4922801&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631427%26dopt%3DAbstract</link>
            <description>Authors: Julius H, Basu D, Ricci E, Wing J, Basu JK, Pocaterra D, Bonfanti P
    South Africa has the highest prevalence of human immunodeficiency virus (HIV) infection in the world. The improved life expectancy, due to the recent introduction of highly active antiretroviral therapy (HAART), may lead to an increased health burden related to metabolic disorders, resulting in an increased pressure on health-care services. The main objective of this study was to determine the prevalence of hypertension, diabetes, obesity and dyslipidemia in a sample of HAART-treated HIV infected patients, attending an HIV clinic in the Gauteng province. This was a cross-sectional study of 304 HIV positive patients enrolled between January 2009 and March 2009, including patients aged 18 to 45 years, on HAART f...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4922801</comments>
            <pubDate>Wed, 01 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4922801</guid>        </item>
        <item>
            <title>HIV-1 Reactivation Induced by Apicidin Involves Histone Modification in Latently Infected Cells.</title>
            <link>http://www.medworm.com/index.php?rid=4922800&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631428%26dopt%3DAbstract</link>
            <description>Authors: Lin S, Zhang Y, Ying H, Zhu H
    The existence of stable, transcriptionally silent human immunodeficiency virus (HIV) in latently infected cells represents a major obstacle to acquired immune deficiency syndrome (AIDS) therapy. Histone deacetylase (HDAC) can inhibit histone acetylation, resulting in HIV-1 provirus transcription silence. Apicidin, a widely used antiparasitic drug, exhibits antiparasitic activity by inhibiting HDAC. Using the latently infected A10.6 cell line, we describe the dose- and time-dependent manner in which Apicidin reverses HIV-1 latency. We found that Apicidin can synergize with trichostatin A (TSA) to activate HIV-1 gene expression. Chromatin immunoprecipitation (ChIP) assay further indicates that Apicidin induces HIV-1 reactivation by increasing the ac...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4922800</comments>
            <pubDate>Wed, 01 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4922800</guid>        </item>
        <item>
            <title>Response to HAART in Treatment-Naive HIV-Infected Patients with a Prior Diagnosis of Tuberculosis or other Opportunistic Infections.</title>
            <link>http://www.medworm.com/index.php?rid=4922799&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21631429%26dopt%3DAbstract</link>
            <description>In conclusion, a previous diagnosis of TB or another ADI before HAART did not compromise short-term virological and immunological response to treatment. A prior diagnosis of an ADI different to TB significantly increased all cause mortality.
    PMID: 21631429 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4922799</comments>
            <pubDate>Wed, 01 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4922799</guid>        </item>
        <item>
            <title>Prospective Observation for Seven-Year's Highly Active Antiretroviral Therapy in Chinese HIV-1 Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=4877094&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21585332%26dopt%3DAbstract</link>
            <description>Authors: He M, Zheng YH, Zhou HY, Mamadou D, Chen Z, Chen X, Yao YH, He Y
    To prospectively observe the efficacy, tolerability, immune reconstitution and toxicity of long-term highly active antiretroviral therapy (HAART) in Chinese patients infected HIV. 437 cases originally received two nucleoside reverse transcriptase inhibitors (NRTIs) and one non-nucleoside reverse transcriptase inhibitor (NNRTI) during a mean period of 4.3 years (3.1-7.3). Patients were followed up by HIV RNA levels, T lymphocyte subsets, blood routine test, and biochemical parameters. If active opportunistic infections, apparent side effects or virological failure appeared, appropriate treatment would be taken immediately. 30 patients (6.86%) died, most in the first 6 months of HAART. The proportion of subjects wi...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877094</comments>
            <pubDate>Tue, 17 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877094</guid>        </item>
        <item>
            <title>Liver-Related Factors Associated with Low Vitamin D Levels in HIV and HIV/HCV Coinfected Patients and Comparison to General Population.</title>
            <link>http://www.medworm.com/index.php?rid=4877093&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21585333%26dopt%3DAbstract</link>
            <description>Conclusions: In our experience, despite the high prevalence of 25(OH)D insufficiency, HIV and HCV-infection did not seem to influence vitamin D status. The role of HIV, HCV and cART on hypovitaminosis D needs further validation in larger cohorts that account for the vitamin levels in general populations and for seasonal and regional variability.
    PMID: 21585333 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877093</comments>
            <pubDate>Tue, 17 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877093</guid>        </item>
        <item>
            <title>Cervical Squamous Intraepithelial Lesions Among HIV-Positive Women on Antiretroviral Therapy in Kenya.</title>
            <link>http://www.medworm.com/index.php?rid=4877092&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21585334%26dopt%3DAbstract</link>
            <description>Conclusion: SIL is prevalent among women on antiretroviral therapy and is associated with immunosuppression, low income, and less frequent condom use. Cervical cancer screening and counseling on condom use should be routinely offered to HIV-infected women in antiretroviral treatment clinics in Africa.
    PMID: 21585334 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877092</comments>
            <pubDate>Tue, 17 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877092</guid>        </item>
        <item>
            <title>Neutral Actions of Raltegravir on Adipogenesis, Glucose Metabolism and Lipolysis in 3T3-L1 Adipocytes.</title>
            <link>http://www.medworm.com/index.php?rid=4877091&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21585335%26dopt%3DAbstract</link>
            <description>Authors: Pérez-Matute P, Pérez-Martínez L, Blanco JR, Oteo JA
    Raltegravir (RAL) has been shown to be virologically effective in both treatment naive and triple class resistant patients. A more favourable metabolic profile associated with RAL in comparison with other antiretroviral drugs has also been observed. The aim of this study was to investigate the molecular mechanisms that could explain the lack of toxicity of this drug in metabolism. Thus, the effects of RAL on adipogenesis and adipocyte metabolism were analyzed using 3T3-L1 cells, a very adequate and convenient cell culture model for the investigation of adipose differentiation and metabolism. The effects of RAL on adipogenesis were evaluated by the Oil Red O staining after 8 days of induction of differentiation. Several ad...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4877091</comments>
            <pubDate>Tue, 17 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4877091</guid>        </item>
        <item>
            <title>HIV Persistence in the Gut Mucosa of HIV-Infected Subjects Undergoing Antiretroviral Therapy Correlates with Immune Activation and Increased Levels of LPS.</title>
            <link>http://www.medworm.com/index.php?rid=4824246&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457131%26dopt%3DAbstract</link>
            <description>Authors: d'Ettorre G, Paiardini M, Zaffiri L, Andreotti M, Ceccarelli G, Rizza C, Indinnimeo M, Vella S, Mastroianni CM, Silvestri G, Vullo V
    We investigated the relationship between viral persistence in the gut, microbial translocation, and T cell activation during chronic HIV infection. Plasma levels of LPS, fraction of circulating CD8+CD38+ T cells, and levels of HIV-DNA in rectosigmoid biopsies and peripheral blood mononuclear cells were determined in 22 HIV-infected individuals and 10 healthy controls. We found that in untreated HIV-infected individuals, HIV-DNA load was higher in the gut mucosa than in the blood. Also, ART-treated patients exhibited lower levels of LPS and CD8+CD38+ T cells than untreated patients, but higher levels than controls. In ART-treated individuals, the ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4824246</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4824246</guid>        </item>
        <item>
            <title>Canada's International Response to HIV during Times of Global Transition: A Qualitative Inquiry.</title>
            <link>http://www.medworm.com/index.php?rid=4824245&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457132%26dopt%3DAbstract</link>
            <description>Conclusions: Lessons from the 2000-2004 era of transition focus on strategic investments, the inextricable connection between HIV and development and strategy coherence. These results highlight that it is more constructive to ensure that Canadian development responses in all areas engage with both the upstream drivers of HIV as well as the impacts of the epidemic itself in order to achieve the greatest results from international investment and the most effective contributions to the lives of the people that these endeavours seek to support.
    PMID: 21457132 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4824245</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4824245</guid>        </item>
        <item>
            <title>Drug Resistance Mutations during Structured Interruptions of HAART in Two HIV-1-Infected Children.</title>
            <link>http://www.medworm.com/index.php?rid=4824244&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457133%26dopt%3DAbstract</link>
            <description>In this study, we searched for antiretroviral drug resistance mutations at the end of five viral rebounds of two children with HIV and a chronically undetectable viral load (VL) who underwent an STI program. The HAART was interrupted for 4 weeks and then restarted and continued for 12 weeks for three cycles. VL, CD4+/CD8+ lymphocytes, and clinical status were evaluated at the end of each STI and at 6 and 12 weeks after HAART was resumed. Treatment of both the patients based on zidovudine+lamivudine+ritonavir remained identical during the study. The reverse transcriptase (RT)- and protease (PR)-coding regions were sequenced at the end of each viral rebound. One patient experienced progressively lower viral rebounds (269000-31300 at the first and third rebounds, respectively), while the othe...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4824244</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4824244</guid>        </item>
        <item>
            <title>Once-a-day (QD) vs. Twice-daily (BID) Nevirapine as Simplification in PI-Treated Patients after 2 mos. of BID Induction.</title>
            <link>http://www.medworm.com/index.php?rid=4668249&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21443516%26dopt%3DAbstract</link>
            <description>Authors: Maserati R, Brandolini M, Cattelan A, Orani A, Sighinolfi L, Andreoni M, Uglietti A, Guaraldi G, Sotgiu G, 
    To assess the efficacy and the tolerability of once-daily (QD) versus twice-daily (BID) nevirapine (NVP)-based highly active antiretroviral therapy (HAART) in virologically suppressed, HIV-positive patients switched from protease inhibitor (PI)-based HAART. Eligible patients were enrolled in the multicenter trial if HIV RNA levels were &amp;lt;50 copies/mL for ³6 months prior. Patients were switched from a PI to NVP 200 mg BID for 2 months, and then randomized to continue with that regimen (group A) or NVP 400 mg QD (group B) for a further 10 months. Virological efficacy (primary endpoint) and tolerability/toxicity were evaluated according to an intention-to-treat analysis....</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4668249</comments>
            <pubDate>Mon, 28 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4668249</guid>        </item>
        <item>
            <title>Application of SCR Priming VLP Boosting as a Novel Vaccination Strategy Against HIV-1.</title>
            <link>http://www.medworm.com/index.php?rid=4668248&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21443517%26dopt%3DAbstract</link>
            <description>Authors: Sadat SM, Zabihollahi R, Aghasadeghi MR, Vahabpour R, Siadat SD, Memarnejadian A, Azadmanesh K, Parivar K
    Human immunodeficiency virus infection is a worldwide health problem and a protective vaccine is desperately needed to control the AIDS pandemics. To address this concern, we previously constructed single-cycle replicable (SCR) HIV-1 virions, which completely maintained the antigenic structures of HIV-1. Herein, to optimize a vaccination strategy, we studied the immunogenicity of produced SCR virions and adjuvant-formulated HIV-1 virus-like particles (VLPs) in homologous and heterologous prime-boosting regimens. Accordingly, BALB/c mice received three doses of immunogens in 3-week intervals and their immune responses were evaluated using ELISA, cytokine and IFN-γ ELISpot ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4668248</comments>
            <pubDate>Mon, 28 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4668248</guid>        </item>
        <item>
            <title>Non-Alcoholic Fatty Liver Disease in HIV Infection Associated with Altered Hepatic Fatty Acid Composition.</title>
            <link>http://www.medworm.com/index.php?rid=4668250&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21434863%26dopt%3DAbstract</link>
            <description>Authors: Arendt BM, Mohammed SS, Ma DW, Aghdassi E, Salit IE, Wong DK, Guindi M, Sherman M, Heathcote EJ, Allard JP
    Hepatic fatty acid (FA) composition, especially a reduction in n-3 polyunsaturated FA (PUFA) may contribute to the pathogenesis of non-alcoholic fatty liver disease (NAFLD), which is common in HIV-infection.. In a cross-sectional study we compared hepatic FA composition between 20 HIV-infected men with NAFLD (HIV/NAFLD), 21 HIV-negative men with NAFLD (NAFLD), and 7 healthy controls. Within HIV/NAFLD we compared simple steatosis (HIV/SS) to steatohepatitis (HIV/NASH). FA composition in liver and erythrocytes, oxidative stress, diet, and exercise were assessed. Major findings (P&amp;lt;0.05) were: 1) higher hepatic n-6/n-3 ratio in HIV/NAFLD [median (range)] [8.08 (1.08-21.52)...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4668250</comments>
            <pubDate>Thu, 24 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4668250</guid>        </item>
        <item>
            <title>Anal Cancer: Focus on HIV-Positive Patients in the HAART-Era.</title>
            <link>http://www.medworm.com/index.php?rid=4607107&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21410431%26dopt%3DAbstract</link>
            <description>Authors: Zanet E, Berretta M, Martellotta F, Cacopardo B, Fisichella R, Tavio M, Berretta S, Tirelli U
    Anal cancer represents an increasing health problem, especially in immune-compromised patients, as HIV-positive patients. Notably, a significant higher incidence rate is reported among HIV infected patients with the advent of highly active antiretroviral therapy (HAART). To date, no randomised trial supports the correlation between existing screening strategies and reduced progression of anal intraepithelial neoplasia (AIN) to anal cancer or improved survival. Nevertheless, screening and treatment of AIN by topical agents should be implemented in high risk population. Data on invasive anal cancer treatment show that combined modality treatment (CMT) is the treatment of choice. Early r...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4607107</comments>
            <pubDate>Tue, 15 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4607107</guid>        </item>
        <item>
            <title>HIV-Infected Patients and Liver Transplantation: Who, When and Why.</title>
            <link>http://www.medworm.com/index.php?rid=4356731&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21222618%26dopt%3DAbstract</link>
            <description>Authors: Tavio M, Grossi P, Baccarani U, Scudeller L, Pea F, Berretta M, Adani G, Vivarelli M, Riva A, Tirelli U, Bresadola V, Viale P, Risaliti A
    Well into the 25th year of the HIV pandemics, and into the 15th year of the highly active antiretroviral therapy (HAART) era, liver transplantation (LT) in the HIV population might be viewed as both a problem and an opportunity. It is still a problem when we consider that only a small proportion of all HIV-infected patients with end stage liver disease (ESLD) will have access to this precious and limited resource. But, in the face of the continuous HAART refinements, that will probably expand in the future the pool of potential HIV- organ recipients, LT is also an opportunity. Considering the poor results observed in a subset of HIV/HCV coin...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4356731</comments>
            <pubDate>Tue, 11 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4356731</guid>        </item>
        <item>
            <title>Aminotransferase Serum Levels Decrease after Initiating Antiretroviral Treatment in HIV Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=4419756&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21214507%26dopt%3DAbstract</link>
            <description>Conclusions: There is a significant decrease in aminotransferase serum levels following the initiation of antiretroviral treatment in HIV infected patients.
    PMID: 21214507 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419756</comments>
            <pubDate>Wed, 05 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419756</guid>        </item>
        <item>
            <title>HIV Infection Induces Morphometrical Changes on The Oral (Buccal mucosa and Tongue) Epithelial Cells.</title>
            <link>http://www.medworm.com/index.php?rid=4419764&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198427%26dopt%3DAbstract</link>
            <description>This study revealed that HIV infection was able to induce morphometrical changes on the oral epithelial cells.
    PMID: 21198427 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419764</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419764</guid>        </item>
        <item>
            <title>A RhoA-Derived Peptide Inhibits Human Immunodeficiency Virus-1 Entry in vitro.</title>
            <link>http://www.medworm.com/index.php?rid=4419763&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198428%26dopt%3DAbstract</link>
            <description>Authors: Maselko M, Ward C, Pastey M
    RhoA-derived peptides have been shown to have antiviral activity against both human respiratory syncytial virus and human parainfluenza virus-3. The present study investigates the toxicity, anti-HIV-1 activity and mechanism of action of a RhoA-derived peptide (RhoA 77-95). The efficacy of this peptide was compared to a scrambled peptide of the same amino acid composition and Enfuvirtide, a HIV entry inhibitor. Our data show that this RhoA-derived peptide is a non-toxic and effective inhibitor of a CXCR4 tropic strain of HIV-1. We also demonstrate that the mechanism of entry inhibition is likely mediated by polyanionic properties and is dependent on the dimerization of peptides.
    PMID: 21198428 [PubMed - as supplied by publisher] (Source: Current ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419763</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419763</guid>        </item>
        <item>
            <title>Cryptogenic Liver Diseases: Sailing by Sight from HIV Co-Infection with Hepatitis Viruses to HIV Mono-Infection Through the Pillars of Hercules.</title>
            <link>http://www.medworm.com/index.php?rid=4419762&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198429%26dopt%3DAbstract</link>
            <description>Authors: Gotti D, Focà E, Albini L, Mendeni M, Vavassori A, Roldan EQ, Torti C
    Liver injury in the HIV-positive population has been classically associated with hepatitis B or C viruses (HBV and HCV). While HBV or HCV co-infections have represented &quot;Pillars of Hercules&quot; for hepatic disease (not further beyond), it is now time to move forward and shed light on liver disease in HIV-infected patients without HBV or HCV co-infections. Indeed, over the last years, liver disease in HIV-mono-infected patients has emerged and fated to become one of the main non AIDS-related complications. Although several cases have specific etiologies (e.g., alcohol abuse), other cases are most challenging for the clinicians because the actual causes are only hypothesized, such as it is difficult to treat the...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419762</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419762</guid>        </item>
        <item>
            <title>Late and Low Compliance with Hepatitis B Serology Screening among HIV-Infected Patients in a Resource-limited Setting: An Issue to Improve HIV Care.</title>
            <link>http://www.medworm.com/index.php?rid=4419761&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198430%26dopt%3DAbstract</link>
            <description>In conclusion, compliance with hepatitis B serology screening was relatively low and late. Educational program regarding hepatitis B serology screening, identification of barriers, and interventions to eliminate these barriers in resource-limited settings are crucial to improve HIV care.
    PMID: 21198430 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419761</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419761</guid>        </item>
        <item>
            <title>Fat Tissue Distribution Changes in HIV-Infected Patients Treated with Lopinavi.</title>
            <link>http://www.medworm.com/index.php?rid=4419760&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198431%26dopt%3DAbstract</link>
            <description>Authors: Kolta S, Flandre P, Van PN, Cohen-Codar I, Valantin MA, Pintado C, Morlat P, Boué F, Rode R, Norton M, Knysz B, Briot K, Roux C, Delfraissy JF
    Given the decline in mortality among HIV-infected patients, it has become increasingly important to consider delayed disease-related and/or anti-HIV therapy-related adverse effects, such as lipodystrophy, when choosing initial therapy. Data from the MONARK trial allowed for comparison of the potential lipodystrophic effects of lopinavir/ritonavir (LPV/r) monotherapy with those of triple therapy with LPV/r plus zidovudine (ZDV) and lamivudine (3TC). This was a randomized, open-label, multinational study that included 136 antiretroviral-naive HIV-infected patients. A portion of study patients underwent evaluations of limb and trunk fat t...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419760</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419760</guid>        </item>
        <item>
            <title>Long-Term Safety from the Raltegravir Clinical Development Program.</title>
            <link>http://www.medworm.com/index.php?rid=4419759&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198432%26dopt%3DAbstract</link>
            <description>Conclusions: Long-term data from the phase III clinical trials demonstrate that raltegravir was generally well-tolerated in both treatment-naïve and treatment-experienced patients with HIV infection.
    PMID: 21198432 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419759</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419759</guid>        </item>
        <item>
            <title>High Mobility Group Box Protein-1 in HIV-1 Infection.</title>
            <link>http://www.medworm.com/index.php?rid=4419758&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198433%26dopt%3DAbstract</link>
            <description>Authors: Trøseid M, Sönnerborg A, Nowa P
    Chronic immune activation driven by microbial translocation from a damaged gut plays a fundamental role in HIV-1 progression. However, the exact link between a leaky gut and immune activation remains to be established. A growing body of evidence suggests that high mobility group box protein-1 (HMGB1) may be involved in this process. HMGB1 is a DNA binding protein present in every nucleated cell, which might be actively secreted to the extracellular milieu by activated cells or passively released from damaged or dying cells. The biological effect depends on its ability to form complexes: HMGB1 alone signals through the receptor of advanced glycosylated end products (RAGE) and promotes regeneration and repair, whereas HMGB1 in complex with bacte...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419758</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419758</guid>        </item>
        <item>
            <title>Accumulation of Defective HIV-1 Variants in a Patient with Slow Disease Progression.</title>
            <link>http://www.medworm.com/index.php?rid=4419757&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21198434%26dopt%3DAbstract</link>
            <description>Authors: Paolucci S, Gulminetti R, Maserati R, Dossena L, Baldanti F
    Viral population in a long term non progressor carrying CRF02-AG HIV-1 virus variants with a truncated RT gene and attenuated virus replication was analyzed. The proportion of mutant and wild-type RT sequences was determined by clonal analysis of HIV-1 DNA and RNA from blood samples and peripheral blood mononuclear cell (PBMC) culture supernatants. Recombinant HIV-1 strains were generated by reverse genetics to evaluate the replicative capacity of RT variants in PBMC cultures. HIV-1 RNA and DNA sequences in PBMC cultures showed a mixture of stop codons (RT(STOP)), recombinant forms, (RT(RF)), and full length (RT(FL)) strains. In plasma, proportion of HIV-1 RNA sequences with a truncated RT gene fluctuated over time (0...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419757</comments>
            <pubDate>Mon, 03 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419757</guid>        </item>
        <item>
            <title>Retroperitoneal Cryptococcoma in a Case of Disseminated Cryptococcosis on Antifungal Maintenance Therapy.</title>
            <link>http://www.medworm.com/index.php?rid=4419767&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21187005%26dopt%3DAbstract</link>
            <description>Authors: Ferraioli G, Cavanna C, Ricciardi M, Daffara S, Sangiovanni L, Filice C, Barbarini G
    Cryptococcoma is a rare entity, characterized by solid, space-occupying masses, usually found in the brain. It has been reported in the setting of &quot;paradoxical&quot; immune reconstitution inflammatory syndrome. A case of retroperitoneal cryptococcoma in a HIV-infected woman with a clinical history of disseminated cryptococcosis on antifungal maintenance therapy is described.
    PMID: 21187005 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419767</comments>
            <pubDate>Fri, 24 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419767</guid>        </item>
        <item>
            <title>Use of highly active antiretroviral therapy is increasing in HIV positive severe drug users.</title>
            <link>http://www.medworm.com/index.php?rid=4419766&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21187006%26dopt%3DAbstract</link>
            <description>Authors: Vallecillo G, Sanvisens A, Martinez E, Torrens M, Bolao F, Tor J, Muga R
    Substance abuse greatly impacts the effectiveness of highly active antiretroviral therapy (HAART). We analyzed antiretroviral use in drug users positive for human immunodeficiency virus (HIV) that sought substance abuse treatment.
    PMID: 21187006 [PubMed - in process] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419766</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419766</guid>        </item>
        <item>
            <title>Rates of initial virological suppression and subsequent virological failure after initiating highly active antiretroviral therapy: the impact of aboriginal ethnicity and injection drug use.</title>
            <link>http://www.medworm.com/index.php?rid=4419765&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21187007%26dopt%3DAbstract</link>
            <description>Authors: Martin LJ, Houston S, Yasui Y, Wild TC, Saunders LD
    To compare rates of initial virological suppression and subsequent virological failure by Aboriginal ethnicity after starting highly active antiretroviral therapy (HAART).
    PMID: 21187007 [PubMed - in process] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4419765</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4419765</guid>        </item>
        <item>
            <title>The significance of HIV-1 genetic diversity for vaccine development.</title>
            <link>http://www.medworm.com/index.php?rid=4356713&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21229664%26dopt%3DAbstract</link>
            <description>Authors: Thomson MM
    
    PMID: 21229664 [PubMed - in process] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4356713</comments>
            <pubDate>Wed, 01 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4356713</guid>        </item>
        <item>
            <title>HIV-1 nef Protein Visits B-Cells via Macrophage Nanotubes: A Mechanism for AIDS-Related Lymphoma Pathogenesis?</title>
            <link>http://www.medworm.com/index.php?rid=4159612&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21067513%26dopt%3DAbstract</link>
            <description>Authors: Lamers SL, Fogel GB, Huysentruyt LC, McGrath MS
    This letter refers to the recent demonstration that HIV-1 infected macrophages form specialized conduits that connect to B-cells (1). The conduit selectively transports the HIV-1 nef protein, providing nef with numerous means to interfere with cellular processes. Currently, no consideration of the connection between the conduit and the development of AIDS-related lymphoma (ARL) has been offered. ARL is one of the primary causes of death in the HIV-infected population and is related to B-cell proliferation and activation. In this letter we discuss several studies that link HIV-infected macrophages and specific forms of the nef protein to the development of ARL. The conduits discovered by Xu et al. [1] may lead to a better understa...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159612</comments>
            <pubDate>Thu, 11 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159612</guid>        </item>
        <item>
            <title>Polyvalent AIDS Vaccines.</title>
            <link>http://www.medworm.com/index.php?rid=4159618&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054250%26dopt%3DAbstract</link>
            <description>Authors: Lu S, Wang S, Grimes Serrano JM
    A major hurdle in the development of a global HIV-1 vaccine is viral diversity. For close to three decades, HIV vaccine development has focused on either the induction of T cell immune responses or antibody responses, and only rarely on both components. After the failure of the STEP trial, the scientific community concluded that a T cell-based vaccine would likely not be protective if the T cell immune responses were elicited against only a few dominant epitopes. Similarly, for vaccines focusing on antibody responses, one of the main criticisms after VaxGen's failed Phase III trials was on the limited antigen breadth included in the two formulations used. The successes of polyvalent vaccine approaches against other antigenically variable pathoge...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159618</comments>
            <pubDate>Fri, 05 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159618</guid>        </item>
        <item>
            <title>HIV-Specific T Cells: Strategies for Fighting a Moving Target.</title>
            <link>http://www.medworm.com/index.php?rid=4159617&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054251%26dopt%3DAbstract</link>
            <description>Authors: McKinnon LR, Kaul R, Herman M, Plummer FA, Ball TB
    HIV vaccine development faces many hurdles, including the failure of empirical approaches, an incomplete understanding of protective immunity, and the extreme genetic diversity of HIV-1. HIV is a moving target in at least two key ways: 1) within an infected individual, years of evolution lead to the formation of quasispecies, and selection of variants with increased fitness, and 2) during the course of the pandemic, subtypes change in frequency as they are transmitted from host to host. In spite of this, CD8+ T cells are often able to overcome HIV diversity, leading to relatively high levels of cross-reactive and cross-clade responses. Recent research suggests that the cross-reactivity of HIV-specific CD8+ T cell responses sho...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159617</comments>
            <pubDate>Fri, 05 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159617</guid>        </item>
        <item>
            <title>HIV-1 Superinfection and its Implications for Vaccine Design.</title>
            <link>http://www.medworm.com/index.php?rid=4159616&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054252%26dopt%3DAbstract</link>
            <description>Authors: Chohan BH, Piantadosi A, Overbaugh J
    HIV-1 superinfection, which refers to a subsequent HIV-1 infection from a different source partner after the first HIV-1 infection is established, has now been well documented in multiple populations. Some studies suggest that the risk of superinfection may be close to that of initial infection, suggesting that the immunity induced by chronic HIV-1 infection may not be adequate to confer protection from another HIV-1 strain. Detailed studies that examined immune responses in individuals who became superinfected generally support this hypothesis, but such studies have been limited. Indeed, superinfection represents one of the few settings, apart from vaccine trials, where there is an opportunity to gain insights into the role of HIV-specific...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159616</comments>
            <pubDate>Fri, 05 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159616</guid>        </item>
        <item>
            <title>Broadly Neutralizing Antibodies and their Significance for HIV-1 Vaccines.</title>
            <link>http://www.medworm.com/index.php?rid=4159615&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054253%26dopt%3DAbstract</link>
            <description>Authors: González N, Alvarez A, Alcamí J
    Despite extensive efforts, a preventive HIV vaccine has not yet been obtained and remains the main challenge in the field of AIDS research. Empirical approaches which have proved successful for many vaccines are not sufficient to tackle HIV-1 and new strategies to design effective preventive AIDS vaccines are critical. To this aim, further understanding of the mechanisms of action of neutralizing antibodies is required. In this review we summarize our current knowledge on the structure of the gp160 viral envelope and the dynamics of viral entry, the evolution of humoral response in HIV-infected patients and the mechanisms of viral escape. Finally, we describe the few neutralizing antibodies with activity against a broad spectrum of circulating...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159615</comments>
            <pubDate>Fri, 05 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159615</guid>        </item>
        <item>
            <title>Correlations Between HIV-1 Clades and HIV-1 Antibody Neutralization Sensitivity: Significant for Vaccine Development?</title>
            <link>http://www.medworm.com/index.php?rid=4159614&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054254%26dopt%3DAbstract</link>
            <description>Authors: van Gils MJ, Schuitemaker H
    The correlates of protection against HIV-1 infection or disease progression are still unknown which causes an immense challenge for HIV-1 vaccine design. Existing effective vaccines against other viruses generate antibodies that either block the initial infection or contribute to the eradication of the virus before it can cause disease. For HIV-1, a protective vaccine capable of eliciting protective neutralizing antibodies does not exist and the difficulties for the generation of such a vaccine are multiple. Conserved elements on the viral envelope glycoprotein, the target of HIV-specific neutralizing antibodies, seem to be poorly immunogenic and attempts to generate an immunogen that can elicit broadly reactive neutralizing antibodies have remained...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159614</comments>
            <pubDate>Fri, 05 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159614</guid>        </item>
        <item>
            <title>Computational Design of Centralized HIV-1 Genes.</title>
            <link>http://www.medworm.com/index.php?rid=4159613&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21054255%26dopt%3DAbstract</link>
            <description>Authors: Arenas M, Posada D
    The extreme genetic diversity of the HIV-1 remains as a daunting challenge for the development of an effective AIDS vaccine. One strategy for creating a single vaccine that protects against the HIV-1 expanding population is to reconstruct centralized immunogenic sequences that minimize the genetic distance to circulating strains that the vaccine is targeting. Such centralized genes can be estimated with inferred consensus, ancestral and center-of-tree sequences. Although the increased breadth of antibody and T-cell responses induced by the centralized vaccines to date are encouraging, they are modest and may only be partly effective in combating HIV-1. One of the reasons of this limited success might be that several features of HIV-1 molecular evolution have...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4159613</comments>
            <pubDate>Fri, 05 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4159613</guid>        </item>
        <item>
            <title>Barriers and Facilitators for Adherence to Antiretroviral Therapy in Papua New Guinea.</title>
            <link>http://www.medworm.com/index.php?rid=4082832&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20946092%26dopt%3DAbstract</link>
            <description>Authors: Kelly A, Worth H, Man N, Nosi S, Emori R, Mek A, Akuani F, Kupul M, Kepa B, Walizopa L, Pirpir L, Cangah B, Siba P, Frankland A, Rawstorne P
    Papua New Guinea (PNG) is in a phase of scaling up access to antiretroviral therapy (ART), and adherence to the newly available drug therapy is becoming an important issue. This paper examines adherence to ART in a sample of 374 HIV-positive people in six provinces in PNG. Participants were recruited to the study using non-probability sampling. Sixty-two % of participants reported complete adherence (no missed or late doses in the past week) and 79% reported not missing any doses in the last week. Revival church members were significantly more likely to report having missing a treatment dose(s) (66%). Those living in the Highlands and tho...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082832</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082832</guid>        </item>
        <item>
            <title>Cofactors for HIV-1 Incidence during Pregnancy and Postpartum Period.</title>
            <link>http://www.medworm.com/index.php?rid=4082831&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20946093%26dopt%3DAbstract</link>
            <description>Conclusions: Repeat HIV-1 testing in early postpartum was highly acceptable and resulted in detection of substantial HIV-1 incidence during pregnancy and postpartum period. Within prevention of mother-to-child HIV-1 transmission programs strategic approaches to prevent maternal HIV-1 acquisition during pregnancy are urgently needed.
    PMID: 20946093 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082831</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082831</guid>        </item>
        <item>
            <title>Effects of Plant Extracts on HIV-1 Protease.</title>
            <link>http://www.medworm.com/index.php?rid=4082830&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20946094%26dopt%3DAbstract</link>
            <description>Authors: Filho JR, de Sousa Falcão H, Batista LM, Filho JM, Piuvezam MR
    Acquired immunodeficiency syndrome (AIDS) is one of the most important public health problems, affecting many people every day. This syndrome is caused by the human immunodeficiency virus (HIV) and the HIV-1 protease plays an essential role by promoting virus maturation and thus infecting new cells. The HIV-1 protease is one of the main targets for anti-HIV drug therapy. The present work is a literature survey of plant extracts whose activity has been studied on HIV-1 protease. Here we list 275 species of medicinal plants, distributed in 99 families, with their place of origin, part used, type of extract, concentration and activity. We aim with this work to provide data that could be used in the research and devel...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082830</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082830</guid>        </item>
        <item>
            <title>The Impact of HAART on HPV-related Cervical Disease.</title>
            <link>http://www.medworm.com/index.php?rid=4082829&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20946095%26dopt%3DAbstract</link>
            <description>The objective of this review is to summarize the last ten years of registry-based and clinical research into the impact of HAART on human papillomavirus (HPV) related cervical disease. Relevant Findings: Compared to their HIV-uninfected counterparts, HIV-infected women have an increased prevalence of HPV infection, increased risk of progression of HPV-related cervical disease, and an increased risk of invasive cervical cancer. While the partial immune reconstitution afforded by HAART might be expected to decrease susceptibility to HPV infection and cervical disease, the local effects of improved immunosurveillance on the cervix are uncertain and the increased longevity of patients on HAART may increase risk of exposure to HPV and provide the time required for progression of cervical diseas...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082829</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082829</guid>        </item>
        <item>
            <title>Do HIV-Infected Immigrants Initiating HAART have Poorer Treatment-Related Outcomes than Autochthonous Patients in Spain? Results of the GESIDA 5808 Study.</title>
            <link>http://www.medworm.com/index.php?rid=4082828&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20946096%26dopt%3DAbstract</link>
            <description>Conclusions: The response to HAART among immigrant patients was similar to that of autochthonous patients, although they had a higher rate of losses to follow-up. Sub-Saharan Africans and immigrant females may need particular measures to avoid barriers hindering antiviral efficacy.
    PMID: 20946096 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082828</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082828</guid>        </item>
        <item>
            <title>Etravirine in the Treatment of HIV-1: A Clinical Overview for Healthcare Professionals.</title>
            <link>http://www.medworm.com/index.php?rid=4082827&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20946097%26dopt%3DAbstract</link>
            <description>Authors: Yeni P, Mills A, Peeters M, Vingerhoets J, Kakuda TN, De Smedt G, Woodfall B
    Current HIV treatment guidelines emphasize the importance of using an active antiretroviral therapy regimen that produces full virologic suppression and immunologic competence, while at the same time providing patients with a favorable safety profile and limited risk for development of drug resistance. Etravirine (TMC125), a recently approved, non-nucleoside reverse transcriptase inhibitor (NNRTI), has shown durable, superior virologic efficacy over placebo in the Phase III, randomized, double-blind DUET trials in 1,203 treatment-experienced, NNRTI-resistant, HIV-1-infected patients. Statistical significance of responses with etravirine over placebo was maintained through Week 24, 48 and 96, regardles...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4082827</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4082827</guid>        </item>
        <item>
            <title>High Levels of CD57+CD28- T-Cells, Low T-Cell Proliferation and Preferential Expansion of Terminally Differentiated CD4+ T-Cells in HIV-Elite Controllers.</title>
            <link>http://www.medworm.com/index.php?rid=3768122&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636274%26dopt%3DAbstract</link>
            <description>In this study, CD57+CD28- phenotype, T-cell activation and levels of proliferating T-cells in elite-controllers were studied in relation to spontaneous virus control. In HIV-controllers, 9% were AIDS-diagnosed and there was a high proportion of women. In elite-controllers, high T-cell CD57+CD28- phenotype and activation levels were found and, interestingly, there was a low proliferation of total and naÃ¯ve T-cells and a high proliferation of the CD4+ TEMRA subset. Low T-cell proliferation and preferential expansion of terminally differentiated effector T-cell subsets could be an important factor for virus control in elite-controllers.
    PMID: 20636274 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768122</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768122</guid>        </item>
        <item>
            <title>Saquinavir/Ritonavir Monotherapy as a New Nucleoside-Sparing Maintenance Strategy in Long-Term Virologically Suppressed HIV-Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3768121&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636275%26dopt%3DAbstract</link>
            <description>Conclusion: SQV/r as monotherapy has proven to be a valid, safe, and economical option for virologically suppressed HIV-infected patients, especially in those who experience intolerance or toxicity with nucleoside analogs.
    PMID: 20636275 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768121</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768121</guid>        </item>
        <item>
            <title>Immunogenicity and Tolerability of Yellow Fever Vaccination in 23 French HIV-Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3768120&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636276%26dopt%3DAbstract</link>
            <description>Conclusions. Yellow fever vaccination was safe and effective in a large majority of this cohort of stable, HIV-infected patients.
    PMID: 20636276 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768120</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768120</guid>        </item>
        <item>
            <title>Comparison of Protease Inhibitor (PI) Resistance-associated Mutations between PI-naÃ¯ve and PI-experienced HIV-1 Infected Patients in Thailand Where Subtype A/E is Predominant.</title>
            <link>http://www.medworm.com/index.php?rid=3768119&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636277%26dopt%3DAbstract</link>
            <description>In conclusion, primary PI-RAMs are observed exclusively among PI-experienced patients whereas secondary PI-RAMs are equally found in both PI-naÃ¯ve and PI-experienced patients. Further studies to define virologic response of HIV-1 subtype A/E to various PIs and clinical validation of PI-RAMs in HIV-1 subtype A/E are essentially needed.
    PMID: 20636277 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768119</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768119</guid>        </item>
        <item>
            <title>Cutaneous Markers of HIV Infection and Progression.</title>
            <link>http://www.medworm.com/index.php?rid=3768118&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636278%26dopt%3DAbstract</link>
            <description>Authors: Ameen M
    Skin and mucosal diseases can be the first manifestation of asymptomatic HIV infection, may indicate advancing immunodeficiency, or may represent systemic opportunistic infections or neoplasms. Mucocutaneous diseases are highly prevalent in the HIV-infected population and multiple pathologies are common particularly with advanced immunosuppression. The dominant HIV-associated skin diseases are infectious and inflammatory and they can cause significant morbidity. Although skin cancers are less common their prognosis is often worse. Clinical presentations are often atypical and may vary depending on the level of immunosuppression. Managing skin disease in the context of advanced immunosuppression is challenging and they often respond poorly to conventional therapies. Thi...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768118</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768118</guid>        </item>
        <item>
            <title>An Effective HIV Vaccine: A Combination of Humoral and Cellular Immunity?</title>
            <link>http://www.medworm.com/index.php?rid=3768117&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636279%26dopt%3DAbstract</link>
            <description>Authors: Benmira S, Bhattacharya V, Schmid ML
    The development of a safe and effective HIV vaccine remains the best hope to control the global HIV epidemic. So far, the different strategies tried for vaccine development have led to disappointing results. The first attempted strategy involved trying to raise neutralizing antibodies to inactivate the virus and prevent infection. Both of Vaxgen's VAX004 and VAX003 phase 3 trials made use of this approach but ultimately failed. Given the difficulties encountered, the focus then shifted to the cell mediated arm of the immune system, the T lymphocytes. However, the phase 2 STEP study, which was aimed to stimulate cell-mediated immunity, was halted in 2007 because it failed to prevent infection and there was an increased incidence of HIV infec...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768117</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768117</guid>        </item>
        <item>
            <title>Preventing HIV Transmission in Married and Cohabiting HIV-Discordant Couples in Sub-Saharan Africa through Combination Prevention.</title>
            <link>http://www.medworm.com/index.php?rid=3768116&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636280%26dopt%3DAbstract</link>
            <description>Authors: Matovu JK
    Most new HIV infections in sub-Saharan Africa now occur in married and cohabiting couples, many of whom do not realize that only one of them may be infected with HIV. HIV-negative individuals living in stable HIV-discordant partnerships (in which one partner is HIV-infected while the other one is not) are twice as likely to get infected with HIV as those living in concordant HIV-negative relationships. Since HIV transmission occurs mainly from HIV-infected persons who are unaware of their status, a combination of interventions including behavioral and biomedical interventions is urgently needed to increase knowledge of HIV status as well as reduce the risk of HIV transmission within married and cohabiting couples. Behavioral interventions include promotion of couples...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768116</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768116</guid>        </item>
        <item>
            <title>Bryostatin-1 Synergizes with Histone Deacetylase Inhibitors to Reactivate HIV-1 from Latency.</title>
            <link>http://www.medworm.com/index.php?rid=3768115&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20636281%26dopt%3DAbstract</link>
            <description>Authors: PÃ©rez M, de Vinuesa AG, Sanchez-Duffhues G, Marquez N, Bellido ML, MuÃ±oz-Fernandez MA, Moreno S, Castor TP, Calzado MA, MuÃ±oz E
    The persistence of latent HIV-infected cellular reservoirs represents the major hurdle to virus eradication on patients treated with HAART. It has been suggested that successful depletion of such latent reservoirs will require a combination of therapeutic agents that can specifically and efficiently act on cells harboring latent HIV-1 provirus. Using Jurkat-LAT-GFP cells, a tractable model of HIV-1 latency, we have found that bryostatin -1 reactivates HIV-1 through a classical PKC-dependent pathway. Bryostatin-1 also activates MAPKs and NF-kappaB pathways and synergizes with HDAC inhibitors to reactivate HIV-1 from latency. Bryostatin-1 downr...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3768115</comments>
            <pubDate>Sun, 18 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3768115</guid>        </item>
        <item>
            <title>Novel vaccines and adjuvants.</title>
            <link>http://www.medworm.com/index.php?rid=3567140&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20462398%26dopt%3DAbstract</link>
            <description>Authors: Buonaguro L
    
    PMID: 20462398 [PubMed - in process] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3567140</comments>
            <pubDate>Sun, 16 May 2010 04:45:28 +0100</pubDate>
            <guid isPermaLink="false">3567140</guid>        </item>
        <item>
            <title>Both HIV-Infection and Long-Term Antiretroviral Therapy are Associated with Increased Common Carotid Intima-Media Thickness In HIV-Infected Adolescents and Young Adults.</title>
            <link>http://www.medworm.com/index.php?rid=3516240&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20426755%26dopt%3DAbstract</link>
            <description>Conclusion: HIV infection and longer duration of cART are associated with higher CCIMT in adolescents and young adults.
    PMID: 20426755 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3516240</comments>
            <pubDate>Wed, 28 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3516240</guid>        </item>
        <item>
            <title>Cystatin C, Adipokines and Cardiovascular Risk In HIV Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3516239&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20426756%26dopt%3DAbstract</link>
            <description>Conclusions: The main results of this study are that HIV positive subjects cART treated with &quot;high&quot; CVR have increased plasma levels of leptin, IL-6, IL-18 and cystatin C and hypoadiponectinemia. Moreover, the positive correlation between CVR and cystatin C found in this study for the first time in HIV positive patients, indicates that cystatin C could serve as early marker of enhanced CVR in the HIV-infected population.
    PMID: 20426756 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3516239</comments>
            <pubDate>Wed, 28 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3516239</guid>        </item>
        <item>
            <title>Enhancing the Delivery of Anti Retroviral Drug &quot;Saquinavir&quot; Across the Blood Brain Barrier using Nanoparticles.</title>
            <link>http://www.medworm.com/index.php?rid=3516238&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20426757%26dopt%3DAbstract</link>
            <description>Enhancing the Delivery of Anti Retroviral Drug &quot;Saquinavir&quot; Across the Blood Brain Barrier using Nanoparticles.
    Curr HIV Res. 2010 Apr 29;
    Authors: Mahajan SD, Roy I, Xu G, Yong KT, Ding H, Aalinkeel R, Reynolds J, Sykes D, Nair BB, Lin EY, Prasad PN, Schwartz SA
    Antiretroviral drugs are ineffective at treating viral infection in the brain because they cannot freely diffuse across the blood-brain barrier (BBB). Therefore, HIV-1 viral replication persists in the central nervous system (CNS) and continues to augment the neuropathogenesis process. Nanotechnology can play a pivotal role in HIV-1 therapeutics as it can increase drug solubility, enhance systemic bioavailability, and at the same time offer multifunctionality. Moreover, following conjugation with transferrin (Tf), thes...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3516238</comments>
            <pubDate>Wed, 28 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3516238</guid>        </item>
        <item>
            <title>An Economic Evaluation of Treatments for HIV-associated Facial Lipoatrophy: A Cost-Utility Analysis.</title>
            <link>http://www.medworm.com/index.php?rid=3516237&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20426758%26dopt%3DAbstract</link>
            <description>CONCLUSION: FLA treatments for PLWH enhance QALYs and meet conventional cost-utility thresholds. The incremental cost per QALY for Polyalkylimide gel was lower than that for Poly-l-lactic acid.
    PMID: 20426758 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3516237</comments>
            <pubDate>Wed, 28 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3516237</guid>        </item>
        <item>
            <title>Mild Improvement in Mitochondrial Function after a 3-Year Antiretroviral Treatment Interruption Despite Persistent Impairment of Mitochondrial DNA Content.</title>
            <link>http://www.medworm.com/index.php?rid=3516236&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20426759%26dopt%3DAbstract</link>
            <description>Conclusions: Mitochondrial function improved during a prolonged antiretroviral treatment interruption despite a decrease in mtDNA levels in PBMCs, probably because of the existence of a mitochondrial transcriptional and translational upregulation mechanism or the reversion of mitochondrial toxicity by a mechanism that is independent of DNA polymerase gamma. The reduction in virus-related mitochondrial damage should be considered another relevant benefit of antiretroviral therapy.
    PMID: 20426759 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3516236</comments>
            <pubDate>Wed, 28 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3516236</guid>        </item>
        <item>
            <title>Susceptibility of HIV-1 to Tipranavir and other Antiretroviral Agents in Treatment-Experienced Patients: The UTILIZE Study.</title>
            <link>http://www.medworm.com/index.php?rid=3429989&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353387%26dopt%3DAbstract</link>
            <description>Conclusions: Overall, 59% of TEPs failing a PI-based regimen had HIV-1 with PI resistance. The majority of these patients' viruses remained sensitive to either tipranavir or darunavir. Investigators used results from resistance assays to construct a new regimen, frequently with newer agents. In PI-experienced patients, tipranavir and darunavir remain the most likely available active PIs.
    PMID: 20353387 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429989</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429989</guid>        </item>
        <item>
            <title>Quality of Life of HIV Patients in a Rural Area of Western Uganda: Impact of a Community-Based Antiretroviral Treatment Program.</title>
            <link>http://www.medworm.com/index.php?rid=3429988&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353388%26dopt%3DAbstract</link>
            <description>Conclusions: The observed improvements in HRQOL demonstrate that positive treatment outcomes can be achieved in CBART programs in rural Uganda. However, some patients appear to experience declines in their overall well-being, despite achieving virological suppression. HRQOL surveys can be useful in identifying these patients, who may require additional attention and support to achieve the full benefits of ART.
    PMID: 20353388 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429988</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429988</guid>        </item>
        <item>
            <title>The Association of Lipodystrophy and Oxidative Stress Biomarkers in HIV-Infected Men.</title>
            <link>http://www.medworm.com/index.php?rid=3429987&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353389%26dopt%3DAbstract</link>
            <description>Authors: Vassimon HS, Deminice R, Machado AA, Monteiro JP, Jordao AA
    The aim of this study was to describe the status of oxidative stress and antioxidant biomarkers and their association with metabolic and body composition components of HIV-lipodystrophy syndrome. In a cross-sectional study of blood samples from HIV-infected men with lipodystrophy syndrome (HIV+LIPO+ = 10), HIV-infected men without lipodystrophy syndrome (HIV+LIPO- = 22), and healthy subjects (control = 12), the following oxidative stress biomarkers were analyzed: total hydroperoxide, thiobarbituric acid reactive substances (TBARS), and advanced oxidation protein products (AOPP). In addition, antioxidant biomarkers, including total glutathione, uric acid, alpha-tocopherol, and metabolic components were tested. Dual-ene...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429987</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429987</guid>        </item>
        <item>
            <title>Involvement of Regulatory T cells in HIV immunopathogenesis.</title>
            <link>http://www.medworm.com/index.php?rid=3429986&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353390%26dopt%3DAbstract</link>
            <description>Authors: Bernardes SS, Borges IK, Lima JE, de Azevedo Oliveira Milanez P, Costa IC, Felipe I, Saridakis HO, Ehara Watanabe MA
    Recently, a mechanism of negative regulation of immune responses by a specialized population of so-called regulatory T cells (Tregs) has become a focus of intense investigation. Through the discovery of transcription factor Foxp3 as a central molecular determinant of Tregs differentiation and function, the complex biology of these cells, including maintenance of immunological tolerance to &quot;self&quot; and regulation of immune responses to pathogens, commensals, and tumors, has become the focus of intense investigation. The ability to control the infection and to delay the progression of the infection to AIDS and/or death is probably regulated by a balance between host...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429986</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429986</guid>        </item>
        <item>
            <title>HIV-Induced Abnormalities in Myelopoiesis and their Recovery Following Antiretroviral Therapy.</title>
            <link>http://www.medworm.com/index.php?rid=3429985&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353391%26dopt%3DAbstract</link>
            <description>Authors: Andrea C, Simona G, Luca B, Guido S, Pietro L, Maria M
    HIV-1 infection is associated with hematologic abnormalities including defective myelopoiesis. Most studies of myelopoiesis during HIV-1 infection were performed using unfractionated bone marrow-derived mononuclear cells, thus resulting in significant inter-individual variability in the numbers of cultured precursors. Here we evaluated the myelopoietic potential of circulating CD34+ progenitors by conducting a longitudinal analysis of antiretroviral therapy (ART)-induced changes of colony forming units-granulocyte and monocyte (CFU-GM) growth. Twelve HIV-infected individuals were studied longitudinally before and after initiation of ART (i.e. at a time when plasma HIV-RNA levels had become undetectable); thirty-one HIV-uni...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429985</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429985</guid>        </item>
        <item>
            <title>A Decrease in the Cellular Phosphodiester to Phosphomonoester Lipidratio is Characteristic of HIV-1 Infection.</title>
            <link>http://www.medworm.com/index.php?rid=3429984&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353392%26dopt%3DAbstract</link>
            <description>Authors: Rozmyslowicz T, Wroblewski K, Moodley J, Gaulton GN
    The ability to detect HIV-1 in tissues that are not readily amenable to biopsy greatly limits the diagnosis and control of HIV infection, and ultimately, our ability to understand HIV-induced disease pathology. In view of this, we explored the utility of diagnostically measuring HIV-1 infection using (31)P nuclear magnetic resonance ((31)P-NMR). (31)P-NMR enables the correlation of infection to changes in the concentration of specific intracellular metabolites, macromolecules and of bioenergetic parameters that are key to mammalian cell physiology. Examples include primary components of biological membranes such as phosphomonoester (PME) and phosphodiester (PDE) lipids. Using (31)P-NMR we found that changes in the ratio of PD...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429984</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429984</guid>        </item>
        <item>
            <title>Role of Dendritic Cells in HIV-Immunotherapy.</title>
            <link>http://www.medworm.com/index.php?rid=3429983&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353393%26dopt%3DAbstract</link>
            <description>Authors: Van Gulck E, Van Tendeloo VF, Berneman ZN, Vanham G, Van Gulck E
    HIV remains one of the most important deadly infections today, due to the lack of a preventive vaccine and limited access to medical care in developing countries. In developed countries, antiretroviral therapy is available, but it can not eliminate the virus, implying that life-long therapy is necessary. Therefore, it is important that other strategies such as therapeutic vaccination will be developed to control virus replication or even eliminate the virus. The major obstacles towards such a strategy are the huge variability of the virus and the profound HIV-induced immune dysfunction. In this review we focus on dendritic cell based immunotherapies against HIV.
    PMID: 20353393 [PubMed - as supplied by publish...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429983</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429983</guid>        </item>
        <item>
            <title>Induction of Protective Immunity against Microbial Challenge by Targeting Antigens Expressed by Probiotic Bacteria to Mucosal Dendritic Cells.</title>
            <link>http://www.medworm.com/index.php?rid=3429982&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353394%26dopt%3DAbstract</link>
            <description>Authors: Mohamadzadeh M
    Efficient vaccines combined with adjuvants potentiate and enhance antibody avidity and increase T cell longevity, particularly in individuals with compromised immunity. The efficacy of a novel vaccine can be improved by specifically targeting its immunogenic subunits and expressing it in live probiotic vector (i.e. Lactobacillus acidophilus) that protects its bioavailability and induces not only mucosal but also systemic immunity against microbes. Accordingly, our data clearly show that specific Lactobacillus species (i.e. L. gasseri) not only optimally activate DCs but also deliver targeted antigens to mucosal DCs via 12-mer peptides derived from a phage display library resulting in robust humoral and T cell immunity against microbial challenge. This effort is ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429982</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429982</guid>        </item>
        <item>
            <title>Mucosal Adjuvants.</title>
            <link>http://www.medworm.com/index.php?rid=3429981&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353395%26dopt%3DAbstract</link>
            <description>Authors: Harandi AM, Medaglini D
    The vast majority of pathogens invade the body through or establish infections in the mucosal tissues. Development of vaccines to combat mucosal infections represents a top priority. Mucosal immunization has recently attracted much interest as a means of generating protective immunity against mucosal pathogens. Conversely, only very few mucosal vaccines are presently approved for human use. The development of a broad range of mucosal vaccines will necessitate the development of safe and effective mucosal adjuvants and delivery systems. Over the past decade, a number of immunomodulatory agents, including toxin based adjuvants, Toll like receptor (TLR) mimetics and non TLR-targeting immunostimulators as well as delivery systems have shown promise for muco...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429981</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429981</guid>        </item>
        <item>
            <title>Toward Integrase Defective Lentiviral Vectors for Genetic Immunization.</title>
            <link>http://www.medworm.com/index.php?rid=3429980&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353396%26dopt%3DAbstract</link>
            <description>Authors: Negri DR, Michelini Z, Cara A
    Genetic immunization with lentiviral vectors is under evaluation as a means for induction of sustained immune response. Lentiviral vectors showed reduced antivector immune responses and efficiently transduce post-mitotic cells in vivo, including antigen presenting cells, such as dendritic cells and macrophages, thus providing a significant benefit over other vector-based antigen delivery platforms. Several evidences indicate that a single immunization with lentiviral vectors induces strong and sustained effector and memory T-cell immune responses, as well as antibody production. New generation of lentiviral vectors with improved biosafety profile are also under development. In particular, integration defective lentiviral vectors have been generate...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429980</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429980</guid>        </item>
        <item>
            <title>Recombinant Mycobacterium bovis BCG as an HIV Vaccine Vector.</title>
            <link>http://www.medworm.com/index.php?rid=3429979&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353397%26dopt%3DAbstract</link>
            <description>Authors: Chapman R, Chege G, Shephard E, Stutz H, Williamson AL
    HIV-1 has resulted in a devastating AIDS pandemic. An effective HIV/AIDS vaccine that can be used to either, prevent HIV infection, control infection or prevent progression of the disease to AIDS is needed. In this review we discuss the use of Mycobacterium bovis BCG, the tuberculosis vaccine, as a vaccine vector for an HIV vaccine. Numerous features make BCG an attractive vehicle to deliver HIV antigens. It has a good safety profile, elicits long-lasting cellular immune responses and in addition manufacturing costs are affordable, a necessary consideration for developing countries. In this review we discuss the numerous factors that influence generation of a genetically stable recombinant BCG vaccine for HIV.
    PMID: 20...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429979</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429979</guid>        </item>
        <item>
            <title>Virus-Like Particles as Particulate Vaccines.</title>
            <link>http://www.medworm.com/index.php?rid=3429978&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20353398%26dopt%3DAbstract</link>
            <description>Authors: Buonaguro L, Tornesello ML, Buonaguro FM
    Particulate structures hold great promise for the development of effective and affordable recombinant prophylactic as well as therapeutic vaccines. Different types of particulate structures, including virus-like particles (VLPs) and virosomes, have been developed depending on the nature of the viral pathogen to be targeted and the type of immune response (humoral vs cellular) to be elicited. Particulate structures allow the insertion or fusion of foreign antigenic sequences, resulting in chimeric particles delivering foreign antigens on their surface. Similarly, they are used as carriers for foreign antigens, including non-protein antigens, via chemical conjugation. Particulate structures, indeed, represent a very efficient system for d...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3429978</comments>
            <pubDate>Fri, 19 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3429978</guid>        </item>
        <item>
            <title>The TLR4 ASP299GLY Polymorphism is a Risk Factor for Active Tuberculosis in Caucasian HIV-Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3375021&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20226000%26dopt%3DAbstract</link>
            <description>Conclusions: We describe an independent association between TLR4 Asp299Gly SNP and active TB in Caucasian Mediterranean HIV-infected patients.
    PMID: 20226000 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3375021</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3375021</guid>        </item>
        <item>
            <title>Evidence for Possible Biological Advantages of the Newly Emerging HIV-1 Circulating Recombinant form (CRF) from Malaysia - CRF33_01B in Comparison to its Progenitors - CRF01_AE and Subtype B.</title>
            <link>http://www.medworm.com/index.php?rid=3359288&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20214658%26dopt%3DAbstract</link>
            <description>Authors: Lau KA, Wang B, Miranda-Saksena M, Boadle R, Kamarulzaman A, Ng KP, Saksena NK, Soriano-Sarabia N
    In Malaysia, co-circulation of CRF01_AE and subtype B has resulted in the emergence of the second generation derivative; CRF33_01B in approximately 20% of its HIV-1 infected individuals. Our objective was to identify possible biological advantages that CRF33_01B possesses over its progenitors. Biological and molecular comparisons of CRF33_01B against its parental subtypes clearly show that CRF33_01B replicated better in activated whole peripheral blood mononuclear cells (PBMCs) and CD4+ T-lymphocytes, but not monocyte-derived macrophages (MDMs). Also, its acquired fitness was greater than CRF01_AE but not subtype B. Moreover, CRF33_01B has higher rate of apoptotic cell death and s...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359288</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3359288</guid>        </item>
        <item>
            <title>The Vpu Protein: New Concepts in Virus Release and CD4 Down-Modulation.</title>
            <link>http://www.medworm.com/index.php?rid=3338878&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201792%26dopt%3DAbstract</link>
            <description>Authors: Ruiz A, Guatelli JC, Stephens EB
    Human immunodeficiency virus type 1 (HIV-1) and several simian immunodeficiency viruses (SIV) encode for a transmembrane protein known as Vpu (viral protein U). While one of the smallest of the HIV-1 proteins, it has two important functions within virus-infected cells. The first of these functions is the down-regulation of the CD4 receptor to prevent its interaction with the HIV-1 envelope glycoprotein. Vpu interacts with the CD4 receptor in the rough endoplasmic reticulum (RER), resulting in its re-translocation across the RER and subsequent degradation via the proteasomal pathway. The second major function of the Vpu protein is to facilitate release of virus from infected cells. Previous studies have shown that virus release is cell type spec...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3338878</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3338878</guid>        </item>
        <item>
            <title>The TLR4 ASP299GLY Polymorphism is a Risk Factor for Active Uberculosis in Caucasian HIV-Infected Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3338876&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20201793%26dopt%3DAbstract</link>
            <description>Conclusions: We describe an independent association between TLR4 Asp299Gly SNP and active TB in Caucasian Mediterranean HIV-infected patients.
    PMID: 20201793 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3338876</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3338876</guid>        </item>
        <item>
            <title>Suboptimal Etravirine Activity is Common During Failure of Nevirapine-based Combination Antiretroviral Therapy in a Cohort Infected with non-B subtype HIV-1.</title>
            <link>http://www.medworm.com/index.php?rid=3288619&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163340%26dopt%3DAbstract</link>
            <description>Conclusion: Etravirine has compromised activity in approximately half of the patients failing nevirapine-based first-line treatment in this cohort, which supports guidelines that caution against using it with NRTIs alone in such patients.
    PMID: 20163340 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288619</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288619</guid>        </item>
        <item>
            <title>Is Metabolic Syndrome Associated To Hiv Infection Per Se? Results From The Hermes Study.</title>
            <link>http://www.medworm.com/index.php?rid=3288618&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163341%26dopt%3DAbstract</link>
            <description>Authors: Bonfanti P, De Socio GL, Marconi P, Franzetti M, Martinelli C, Vichi F, Penco G, Madeddu G, Orofino G, Valsecchi L, Vitiello P, Menzaghi B, Magni C, Ricci E
    HERMES is a prospective study including all treatment-na&amp;#xEF;ve patients attending scheduled visits at hospitals in the CISAI group in 2007. The present cross-sectional analysis aims to assess the baseline prevalence and characteristics of Metabolic Syndrome (MS) in a population of HIV-positive treatment-na&amp;#xEF;ve patients. MS was diagnosed using the National Cholesterol Education Program (NCEP) definitions. A total of 292 subjects were enroled, median age was 37 years, 75% of them were males. The prevalence of MS was 12.3%. The most frequent trio of abnormalities that led to the diagnosis of MS was high blood pressure, ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288618</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288618</guid>        </item>
        <item>
            <title>Hepatitis C Infection on Immune Recovery in HIV-Positive Patients on Successful HAART: The Role of Genotype 3.</title>
            <link>http://www.medworm.com/index.php?rid=3288617&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163342%26dopt%3DAbstract</link>
            <description>Conclusions: A blunted early immune recovery was observed in HCV infected patients, compared with HCV negative subjects, while late immune recovery was not different among HCV infected as a whole and not infected subjects; only the subgroup of subjects infected with genotype 3 showed an impaired late immune recovery.
    PMID: 20163342 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288617</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288617</guid>        </item>
        <item>
            <title>Stability of Dried Blood Spots for HIV-1 Drug Resistance Analysis.</title>
            <link>http://www.medworm.com/index.php?rid=3288616&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163343%26dopt%3DAbstract</link>
            <description>Authors: Hearps AC, Ryan CE, Morris LM, Plate MM, Greengrass V, Crowe SM
    The wide scale application of dried blood spots (DBS) as a collection tool for low-cost HIV drug resistance testing requires a greater understanding of the accuracy of DBS for genotype analysis and the stability of DBS under various environmental conditions. Analysis of a 50microl DBS via a single amplicon, nested PCR-based in-house assay (the Burnet genotyping assay) showed an average nucleotide concordance of 98.9% with plasma samples, although only 65% of nucleotide mixtures detected in plasma were also detected within DBS. The analysis of three DBS resulted in the detection of a greater number of nucleotide mixtures (72 and 109 mixtures detected within one and three DBS, respectively, n=10). Two DBS extraction...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288616</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288616</guid>        </item>
        <item>
            <title>Induction of SIV p27-Specific Multifunctional T Cells in the Gut Following Prime-Boost Immunization with Clostridium perfringens and Adenovirus Vaccines Expressing SIV p27.</title>
            <link>http://www.medworm.com/index.php?rid=3288615&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163344%26dopt%3DAbstract</link>
            <description>Authors: Helmus RA, Poonam P, Caruso L, Gupta P, Chen Y
    A vaccine-induced cellular immune response to simian immunodeficiency virus (SIV) in the gut mucosal tissue may prevent the establishment or severity of new SIV infection. An oral Clostridium perfringens expressing SIV p27 (Cp-p27) vaccine that delivers SIV p27 to the gut was evaluated for its ability to prime multifunctional cellular immunity in the gut mucosa. Gut Peyer's patches dendritic cells matured in response to in vitro exposure to Cp-p27 and stimulated production of p27-specific IFN-gamma. In mice, the oral vaccination with the Cp-p27 vaccine and systemic immunization with adenovirus expressing SIV p27 (Ad-p27) induced robust systemic and mucosal immune responses. Furthermore, the prime-boost regimen induced p27-specific...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288615</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288615</guid>        </item>
        <item>
            <title>Nucleoside Analog Stavudine Depletes Mitochondrial DNA with no Organelle Loss in Mouse Oocytes.</title>
            <link>http://www.medworm.com/index.php?rid=3288614&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163345%26dopt%3DAbstract</link>
            <description>Authors: Bostan A, Demeestere I, Vanderwinden JM, Devreker F, Englert Y
    Nucleoside reverse transcriptase inhibitors (NRTIs) are the basis of antiretroviral treatment of HIV-positive patients. Several studies have shown decreased fertility and fecundity among HIV-positive women under antiretroviral treatment. Oocyte impaired competence has been hypothesized to be one of the main mechanisms underlying of this decreased fertility. NRTI side effects are thought to be due to the induced mitochondrial dysfunction. Stavudine, a widely used NRTI, causes persistent mitochondrial damage in various tissues. In order to gain insights into possible mechanisms of HIV-related diminished fertility, we studied the effects of stavudine on mouse oocyte mitochondria. Mitochondrial volume, protein assay an...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288614</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288614</guid>        </item>
        <item>
            <title>Does HIV VCT Reduce Risk Behaviors? An Observational Study in Guatemala City.</title>
            <link>http://www.medworm.com/index.php?rid=3288613&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163346%26dopt%3DAbstract</link>
            <description>Conclusions: Voluntary counseling and testing resulted in changes in some self-reported risk behaviors, but only among HIV positive subjects. On nearly all measures men report riskier behavior than women. Alcohol is the most commonly used drug in this population and is often used with sex.
    PMID: 20163346 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288613</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288613</guid>        </item>
        <item>
            <title>In Patients with HIV-Infection, Chromium Supplementation Improves Insulin Resistance and Other Metabolic Abnormalities: A Randomized, Double-Blind, Placebo Controlled Trial.</title>
            <link>http://www.medworm.com/index.php?rid=3288612&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163347%26dopt%3DAbstract</link>
            <description>Authors: Aghdassi E, Arendt BM, Salit IE, Mohammed SS, Jalali P, Bondar H, Allard JP
    Chromium is an essential micronutrient; chromium deficiency has been reported to cause insulin resistance, hyperglycemia and hyperlipidemia. The aim was to investigate the effect of chromium supplementation on insulin-resistance, other metabolic abnormalities, and body composition in people living with HIV. This was a randomized, double-blind, placebo-controlled trial. Fifty-two HIV-positive subjects with elevated glucose, lipids, or evidence of body fat redistribution, and who had insulin-resistance based on the calculation of homeostasis model of assessment (HOMA-IR &amp;gt;/= 2.5) were assessed. Subjects who were on insulin or hypoglycemic medications were excluded. Subjects were randomized to receive e...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288612</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288612</guid>        </item>
        <item>
            <title>Relationship Power in the Couple and Sexual Double Standard as Predictors of the Risk of Sexually Transmitted Infections and HIV: Multicultural and Gender Differences.</title>
            <link>http://www.medworm.com/index.php?rid=3288611&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163348%26dopt%3DAbstract</link>
            <description>Authors: Berm&amp;#xFA;dez MP, Castro A, Gude F, Buela-Casal G
    The goal of this work is to determine whether relationship power in couples and sexual double standard can predict the risk of sexually transmitted infections/human immunodeficiency virus (STI/HIV) as a function of cultural and gender differences. The sample was made up of 689 adolescents living in Spain, of both sexes, aged between 14 and 19 years, who were sexually active in the past six months and who had a stable partner. Of them, 58.9% were native Spaniards and 41.1% were immigrants of Latin American origin. The results show that origin, age, double standard and the control over decision-making in the couple can predict the risk of STI/HIV; thus, the immigrants, the older participants, those who scored higher in double sta...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288611</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288611</guid>        </item>
        <item>
            <title>Results of a Community-Based Antiretroviral Treatment Program for HIV-1 Infection in Western Uganda.</title>
            <link>http://www.medworm.com/index.php?rid=3288610&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163349%26dopt%3DAbstract</link>
            <description>Conclusion: The findings show that outcomes of a CBART intervention in a rural area compare favorably to outcomes of hospital-based care. If the study results are sustainable over a longer time period, this model could be considered for ART roll-out to impoverished rural/remote populations in Uganda and elsewhere.
    PMID: 20163349 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288610</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288610</guid>        </item>
        <item>
            <title>Hodgkin Lymphoma in HIV Positive Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3288609&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163350%26dopt%3DAbstract</link>
            <description>Authors: Mounier N, Spina M, Spano JP
    Hodgkin Lymphoma (HL) represents one of the most common types of a non-AIDS-de fi ning tumour that occurs in the HIV population, and its incidence is increasing in the post Highly Active Anti-retroviral Therapy (HAART) era. Despite the aggressiveness of that disease, the outcome of patients with HIV-HL has improved with better, combined antineoplastic and antiretroviral approaches. New and effective antiretroviral drugs, in conjunction with nucleoside analogs, improve the control of the underlying HIV infection when used during treatment of HL with chemotherapy. The inclusion of hematopoietic growth factors in the treatment of patients with HIV-HL may allow for the administration of higher dose-intensity chemotherapy and the prolonged use of antire...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288609</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288609</guid>        </item>
        <item>
            <title>SRLVs: a Genetic Continuum of Lentiviral Species in Sheep and Goats with Cumulative Evidence of Cross Species Transmission.</title>
            <link>http://www.medworm.com/index.php?rid=3288608&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163351%26dopt%3DAbstract</link>
            <description>Authors: Caroline L, Juliano C, Minardi C, Jean-Fran&amp;#xE7;ois M
    Lentiviruses from distinct animal species have in common their genomic organization, the induction of slowly progressive diseases over months or years, the large spectrum of induced symptoms and concerned organs, the frequent inapparent infection without any detectable clinical signs, their ability to persist into their hosts despite an often strong and mature immune response.... Lentiviruses are also characterized by their genomic plasticity and the rapid evolution of the viral species. SRLVs infecting goats and sheep follow a genomic evolution pattern similar to that observed in HIV or in other lentiviruses. Based on limited number of complete sequences, they have been initially described as two distinct genetic groups e...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288608</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288608</guid>        </item>
        <item>
            <title>Molecular and Biological Characterization of Equine Infectious Anemia Virus Rev.</title>
            <link>http://www.medworm.com/index.php?rid=3288607&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163352%26dopt%3DAbstract</link>
            <description>Authors: Carpenter S, Dobbs D
    Equine infectious anemia virus (EIAV) is one of the most divergent members of the lentivirus subfamily of 3 retroviruses and is considered a useful comparative model for molecular studies of lentivirus replication. The 4 Rev protein of EIAV is functionally homologous with other lentiviral Revs and facilitates export of 5 incompletely spliced viral mRNAs through a Crm1-dependent pathway. The trans- and cis-acting elements 6 that mediate EIAV Rev function are similar to, but distinct from, the well-characterized elements in human 7 immunodeficiency virus (HIV-1), the prototypical Rev protein. In addition, the EIAV rev sequence is highly 8 variable in vivo, and changes in Rev phenotype correlate with changes in clinical stages of EIAV infection. 9 This review...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288607</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288607</guid>        </item>
        <item>
            <title>EIAV Envelope Diversity: Shaping Viral Persistence and Encumbering Vaccine Efficacy.</title>
            <link>http://www.medworm.com/index.php?rid=3288606&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163353%26dopt%3DAbstract</link>
            <description>Authors: Craigo JK, Montelaro RC
    Equine infectious anemia virus (EIAV) and its associated disease have presented a considerable challenge to veterinary medicine worldwide ever since its identification in the 19(th) century. Furthermore EIAV, along with its fellow animal lentiviruses, has been utilized as an animal model of HIV-1/AIDS research since the latters identification in the late 20(th) century. Like all lentiviruses, EIAV has been shown to have a high propensity for genomic sequence and antigenic variation, principally in its envelope (Env) proteins. However, unlike other lentiviruses, EIAV possesses a unique and dynamic disease presentation that enables consummate analyses of the interactions between a virus, host immune system, and the effects of viral evolution on vaccine ef...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288606</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288606</guid>        </item>
        <item>
            <title>Feline Immunodeficiency Virus (FIV) as A Model for Study of Lentivirus Infections: Parallels with HIV.</title>
            <link>http://www.medworm.com/index.php?rid=3288605&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163354%26dopt%3DAbstract</link>
            <description>Authors: Elder JH, Lin YC, Fink E, Grant CK
    FIV is a significant pathogen in the cat and is, in addition, the smallest available natural model for the study of lentivirus infections. Although divergent at the amino acid level, the cat lentivirus has an abundance of structural and pathophysiological commonalities with HIV and thus serves well as a model for development of intervention strategies relevant to infection in both cats and man. The following review highlights both the strengths and shortcomings of the FIV/cat model, particular as regards development of antiviral drugs.
    PMID: 20163354 [PubMed - as supplied by publisher] (Source: Current HIV Research)</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288605</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288605</guid>        </item>
        <item>
            <title>Virulence Determinants of Equine Infectious Anemia Virus.</title>
            <link>http://www.medworm.com/index.php?rid=3288604&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163355%26dopt%3DAbstract</link>
            <description>Authors: Payne SL, Fuller FJ
    Equine infectious anemia virus (EIAV) is a macrophage-tropic lentivirus that rapidly Induces disease in experimentally infected horses. Because EIAV infection and replication is centered on the monocyte/macrophage and has a pronounced acute disease stage, it is a useful model system for understanding the contribution of monocyte/macrophages to other lentivirus-induced diseases. Genetic mapping studies utilizing chimeric proviruses in which parental viruses are acutely virulent or avirulent have allowed the identification of important regions that influence acute virulence. U3 regions in the viral LTR, surface envelope (SU) protein and the accessory S2 gene strongly influence acute disease expression. While the chimeric proviruses provide insight into genes ...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288604</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3288604</guid>        </item>
        <item>
            <title>Jembrana Disease Virus: Host Responses, Viral Dynamics and Disease Control.</title>
            <link>http://www.medworm.com/index.php?rid=3288603&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163356%26dopt%3DAbstract</link>
            <description>Authors: Desport M, Lewis J
    Jembrana disease virus (JDV) is the most recently discovered member of the lentivirus family and causes an acute clinical disease in Bali cattle with a fatality rate of approximately 15%. It is genetically related to bovine immunodeficiency virus (BIV) to the extent that infections cannot yet be differentially diagnosed using serological assays due to cross-reacting epitopes. Despite their close genetic relationship the pathogenesis of JDV infection in Bali cattle is very different to that of BIV in cattle and is unusual for a member of this virus family. The dynamics of JDV replication and clearance during the acute stage of Jembrana disease, the viral tropism, molecular analysis of the viral genome and mRNA transcripts, and the current status of vaccine de...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288603</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>Small Ruminant Lentiviruses and Human Immunodeficiency Virus: Cousins that Take a Long View.</title>
            <link>http://www.medworm.com/index.php?rid=3288602&amp;cid=s_37271_20_f&amp;fid=37271&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20163357%26dopt%3DAbstract</link>
            <description>Authors: Blacklaws B, Harkiss GD
    Small ruminant lentiviruses (SRLV) and human immunodeficiency viruses (HIV) are related retroviruses that cause multisystem disease usually over a long period of time. The viruses show similarities and differences in biological and pathogenic features. The basic retroviral genomic organization is complicated by the presence of a variable number of accessory genes in both viruses, though the structure is more complex in HIV. Both are mucosal pathogens, and infect cells of the monocyte-macrophage lineage. The main difference in cell tropism is that, unlike HIV, SRLV do not infect lymphocytes. A major feature of both pathogens is restricted replication and virus latency, which are partly responsible for the establishment of chronic infection usually lastin...</description>
            <author>Current HIV Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3288602</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
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