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        <title>Biotherapy 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 'Biotherapy' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Biotherapy&t=Biotherapy&s=Search&f=source]]></link>
        <lastBuildDate>Sat, 10 Oct 2009 19:28:42 +0100</lastBuildDate>
        <item>
            <title>Preface</title>
            <link>http://www.medworm.com/index.php?rid=778848&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd6750u131551j21l%2F</link>
            <description>Content TypeJournal Article

	
		JournalBiotherapyOnline ISSN 1573-8280Print ISSN 0921-299X
	
		Journal VolumeVolume 10
	
		Journal IssueVolume 10, Number 3 / March, 1998 (Source: Biotherapy)</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778848</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:41 +0100</pubDate>
            <guid isPermaLink="false">778848</guid>        </item>
        <item>
            <title>Heat shock proteins and the antitumor T cell response</title>
            <link>http://www.medworm.com/index.php?rid=778840&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv34l0q758x78102j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Heat shock proteins (HSP) have been shown to participate in the antitumor T cell response. First, HSP play a crucial role
 in the intracellular pathway for antigen processing where HSP can make complexes with a broad spectrum of cellular proteins
 and peptides through their chaperone functions. In this pathway, macrophages are required for processing the chaperoned peptides
 to make stable molecules with the major histocompatibility complex (MHC) class I molecules, even when HSP-peptide complexes
 are exogenously administered. Through this pathway, vaccination with HSP-peptide complexes is thus able to elicit the response
 of CD8+ T cells specific for the chaperoned peptides. These findings suggest an essential role of HSP in ‘cross-priming’ and their
 usefulness fo...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778840</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:41 +0100</pubDate>
            <guid isPermaLink="false">778840</guid>        </item>
        <item>
            <title>Antigen-specific therapies in multiple sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=778834&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5658t2425n121193%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Multiple sclerosis is the major neurological disease of young adults in the western world, affecting about 1 per 1,000. It
 is characterised by chronic or recurrent lesions of inflammatory damage in the white matter of the central nervous system.
 Within such lesions, the protective myelin sheath is stripped off axons by infiltrated macrophages which leads to impaired
 conductivity. The inflammatory process most likely starts by activation of helper T cells directed against local myelin antigens.
 Currently, efforts are directed at specifically blocking such myelin-reactive helper T cells in order to control the disease.
 
 In this chapter, immunological features of multiple sclerosis and the experimental animal model for the disease, experimental
 allergic encephalomye...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778834</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:41 +0100</pubDate>
            <guid isPermaLink="false">778834</guid>        </item>
        <item>
            <title>Immune responses to stress proteins: Applications to infectious disease and cancer</title>
            <link>http://www.medworm.com/index.php?rid=2503764&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk277w7w672752783%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Heat shock proteins, or stress proteins have been identified as part of a highly conserved cellular defence mechanism mediated
 by multiple, distinct gene familes and corresponding gene products. As intracellular chaperones, stress proteins participate
 in many essential biochemical pathways of protein maturation and function active during times of stress and during normal
 cellular homeostasis. In addition to their well-characterized role as protein chaperones, stress proteins are now realized
 to possess another important biological property: immunogenicity. Stress proteins are now understood to play a fundamental
 role in immune surveillance of infection and malignancy and this body of basic research has provided a framework for their
 clinical application. As key ta...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503764</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">2503764</guid>        </item>
        <item>
            <title>HLA-DR/DQ Transgenic, class II deficient mice as a novel model to select for HSP T cell epitopes with immunotherapeutic or preventative vaccine potential</title>
            <link>http://www.medworm.com/index.php?rid=2503763&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb20716136k134665%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Protective immunity against mycobacteria is dependent on antigen/MHC class II specific, CD4+ Th1 cells. HLA-DR3-restricted Th1 cells respond to a subset of mycobacterial antigens, including the immunodominant hsp65,
 and recognize a single epitope in hsp65, notably p1-20. Altered peptide ligands (APL) of p1-20 can inhibit p1-20/hsp65-induced
 proliferation of DR3-restricted T cells in an allele specific mannerin vitro. In order to develop a preclinical model in which p1-20 APL can be testedin vivo in the context of HLA, we have used murine class II deficient, HLA transgenic (Ab0) mice, in which all CD4+ T cells are restricted by the tg HLA molecule. BCG-immunized DR3.Ab0 and DQ8.Ab0 mice both responded well to hsp65. Furthermore, DR3.Ab0 mice recognized precisely the sa...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503763</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">2503763</guid>        </item>
        <item>
            <title>Nasal administration of arthritis-related T cell epitopes of heat shock protein 60 as a promising way for immunotherapy in chronic arthritis</title>
            <link>http://www.medworm.com/index.php?rid=2503762&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F418nk1657w023831%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adjuvant Arthritis (AA) can be induced in Lewis rats by immunisation with mycobacterial antigens. The disease can be passively
 transferred with T cell clone A2b, which recognises the 180–188 amino acid sequence in mycobacterial heat shock protein 60
 (hsp60) and which crossreacts with crude cartilage proteoglycans. We succeeded to induce peripheral tolerance to this AA-associated
 T cell epitope following nasal administration of a peptide containing this epitope (mycobacterial hsp60 176–190). In rats
 treated nasally with 176–190 and immunised with mycobacterial hsp60, proliferative responses to 176–190 were reduced. AA was
 inhibited nasally with 176–190 treated rats and not in rats nasally treated with a control mycobacterial hsp60 peptide (211–225).
 Mor...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503762</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">2503762</guid>        </item>
        <item>
            <title>Mucosal modulation of immune responses to heat shock proteins in autoimmune arthritis</title>
            <link>http://www.medworm.com/index.php?rid=2503761&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl5t37238065431t3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Induction of oral tolerance to antigens that are targets of self-reactive immune responses is an attractive approach to antigen-specific
 immune therapy of autoimmune diseases. Oral tolerization has indeed proven to be safe and effective in amelioration of autoimmune
 diseases in animal models. In humans, results have been somewhat controversial. The emphasis given to clinical outcome rather
 than to immunomodulation, and the difficulty in identifying appropriate candidate antigens contribute to the controversy.
 Heat shock proteins are promising targets for immune intervention. Immune reactivity to heat shock proteins has indeed been
 correlated with autoimmune arthritis in animal models, and abnormal immune responses to heat shock proteins have been described
 in huma...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503761</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">2503761</guid>        </item>
        <item>
            <title>Oral administration of HSP-containing E.Coli extract OM-89 has suppressive effects in autoimmunity. Regulation of autoimmune processes by modulating peripheral immunity towards hsp’s?</title>
            <link>http://www.medworm.com/index.php?rid=2503760&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc3n3515t8h2t4184%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;OM-89 (Subreum) is anE. coli extract used for oral administration in the treatment of rheumatoid arthritis. It contains bacterial heat shock proteins,
 namely hsp60 and hsp70, which were shown to be major immunogenic constitutents of the drug. Immunity to bacterial heat-shock
 antigens was shown to be a means of immunomodulation of (experimental) autoimmune disease and possibly inflammation in general.
 This was demonstrated for mycobacterial hsp60 respectively hsp70 in autoimmune disease models for arthritis, diabetes and
 encephalitis. Parallel to the effects displayed by immunisation with hsp, oral administration of hsp-containing OM-89 was
 found to modify autoimmune disease in a number of animal models, such as for arthritis, diabetes and SLE. In rats immunisation
...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503760</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">2503760</guid>        </item>
        <item>
            <title>Heat shock proteins as potential targets in the therapy of inflammatory arthritis</title>
            <link>http://www.medworm.com/index.php?rid=778847&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu2x5lwp7v7m04443%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Whether heat shock proteins (hsp) will be therapeutic targets in arthritis depends on their role in pathogenesis. In this
 article, three possibilities are considered. Firstly, an excessive immune response to bacterial hsp could be arthritogenic
 — as may occur in reactive arthritis. In these circumstances therapy would be directed to down-regulating this immune response,
 or altering the nature of the immune response e.g. by changing cytokine production from interferon-g to IL-4. However this
 approach depends on the immune response to bacterial hsp not being critical for control of the bacterial infection. Secondly,
 an immune response to bacterial hsp may induce autoimmunity by cross-reactivity, e.g. with the homologous human. This could
 also be modulated in the s...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778847</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">778847</guid>        </item>
        <item>
            <title>The expression of potency of neutralizing antibodies for interferons and other cytokines</title>
            <link>http://www.medworm.com/index.php?rid=778845&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F311546753572178t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The occurrence of antibody formation in patients administered biologically active human proteins as biotherapy for different
 diseases emphasizes the importance of establishing a common method of reporting neutralizing antibody levels for such cytokines.
 For quantitative neutralization bioassays, the preferred expression of the neutralizing potency of an antiserum is a titer,
 that is, the dilution of serum that reduces 10 Laboratory Units (LU)/ml of the cytokine to 1 Laboratory Unit/ml, the endpoint
 of most bioassays. This 10-to-1 LU/ml expression, which has been recommended by the World Health Organization for recording
 the results of interferon neutralization by the constant interferon method (with varying dilutions of serum) can also be used
 with the constant an...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778845</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:40 +0100</pubDate>
            <guid isPermaLink="false">778845</guid>        </item>
        <item>
            <title>Anti-cytokine autoantibodies: Epiphenomenon or critical modulators of cytokine action</title>
            <link>http://www.medworm.com/index.php?rid=2503765&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2375421x301w0099%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Low amounts of high-affinity autoantibodies to various cytokines have been detected in sera from healthy donors. Their levels,
 although highly variable, are increased in the circulation of patients subjected to cytokine therapy or suffering from a variety
 of immunoinflammatory diseases. It has been suggested that these autoantibodies play a regulatory role in the intensity and
 duration of an immune response. The antibodies may prevent the binding of a cytokine to its specific cell surface receptor
 thereby neutralizing its biological activityin vivo. They may also act as carrier proteins preventing the rapid elimination of a cytokine from the circulation and thus increase
 its bioactivity. Additionally or alternatively, autoantibodies may modulate cytokine-induced in...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503765</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:39 +0100</pubDate>
            <guid isPermaLink="false">2503765</guid>        </item>
        <item>
            <title>Natural antibodies to interferon-gamma</title>
            <link>http://www.medworm.com/index.php?rid=778851&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr30l32r11u134405%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Natural antibodies to interferon (IFN)-γ were detected in the serum of virus-infected patients and also, at a low titre, in
 the serum of healthy subjects. The increased titre of antibodies to IFN-γ in the sera of virus-infected patients, and its
 decrease with clinical resolution, indicate that these antibodies are related to viral infection and probably reflect IFN-γ
 production as a result of antigenic stimulationin vivo. Natural antibodies to IFN-γ were affinity purified and studied for their capability to interferein vitro with the multiple activities of the lymphokine. Data obtained show that these human anti-IFN-γ antibodies have no inhibitory
 effect on the antiviral and antiproliferative activity of IFN-γ and do not interfere with the binding of the lymph...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778851</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:39 +0100</pubDate>
            <guid isPermaLink="false">778851</guid>        </item>
        <item>
            <title>Potential therapeutic use of antibodies directed towards HuIFN-γ</title>
            <link>http://www.medworm.com/index.php?rid=778850&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa57805g123qgrm17%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;IFN-γ is an important regulator of immune responses and inflammation. Studies in animal models of inflammation, autoimmunity,
 cancer, transplant rejection and delayed-type hypersensitivity have indicated that administration of antibodies against IFN-γ
 can prevent the occurrence of diseases or alleviate disease manifestations. Therefore, it is speculated that such antibodies
 may have therapeutical efficacy in human diseases. Since animal-derived antibodies are immunogenic in patients several strategies
 are being developed in order to reduce or abolish this human anti-mouse antibody (HAMA) response. In our laboratory, we have
 constructed a single-chain variable fragment (scFv) derived from a mouse antibody with neutralizing potential for human IFN-γ.
 A scFv consi...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778850</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:39 +0100</pubDate>
            <guid isPermaLink="false">778850</guid>        </item>
        <item>
            <title>Measurement of cytokine antibodies. Test development</title>
            <link>http://www.medworm.com/index.php?rid=778838&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftx8657l650n21r57%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Several assays have been used for detection of antibodies against cytokines. The choice of assay is greatly dependent on the
 intended goal, e.g. detection of naturally occurring antibodies or therapy induced antibodies. The different assays can be
 grouped in 2 categories. The interference or indirect assays are based on the detection of the test sample interference with
 the biological activity, with detection of the cytokine in EIA or with binding to cellular receptors. In direct assays cytokine
 antibodies are detected by binding to solid phase fixed cytokines, followed by incubation with a secondary enzyme-labelled
 anti-human Ig antibody or by binding to125I-labelled cytokines in RIA.
 
	Content TypeJournal Article

	
		JournalBiotherapyOnline ISSN 1573-8280Print ...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778838</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:39 +0100</pubDate>
            <guid isPermaLink="false">778838</guid>        </item>
        <item>
            <title>Structure-activity of type I interferons</title>
            <link>http://www.medworm.com/index.php?rid=778836&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjg67g6252840v5u2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Type I IFNs constitute a family of proteins exhibiting high homology in primary, secondary, and tertiary structures. They
 interact with the same receptor and transmit signals to cellular nucleus through a similar mechanism, eliciting roughly homogeneous
 biological activity. Nevertheless, the members of that family, IFNα species, IFNβ and IFNω, due to local differences in the structure sometime show distinct properties. From the reported data it results that even
 minute changes or differences in the primary sequences could be responsible for a significant variety of biological actions,
 thus inducing to the hypothesis that Type I IFNs, rather than to be the result of a redundant replication during the evolution,
 play definite roles in the defense of living organis...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778836</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:39 +0100</pubDate>
            <guid isPermaLink="false">778836</guid>        </item>
        <item>
            <title>Treatment of head and neck cancers with BRMs</title>
            <link>http://www.medworm.com/index.php?rid=2678171&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F875777437v145644%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It has been reported that immunologic function is deteriorated in head and neck cancer patients by primary therapies such
 as surgery, irradiation and chemotherapy or tumor itself. As previously described by us, immunologic dysfunction in such patients
 may be recovered by treatment with BRMs.
 
 In the present study, we investigated the effects of BRMs on survival of patients who had primarily been treated in our clinic.
 Fifty-one patients (23 patients; Stage I or Stage II, 28 patients; Stage III or Stage IV) were treated with BRMs (BRM group),
 and 49 patients (22 patients; Stage I or Stage II, 27 patients; Stage III or Stage IV) were employed as controls (Control
 group). The results obtained were as follows: (1) In patients of all Stages, the survival period was si...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2678171</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:38 +0100</pubDate>
            <guid isPermaLink="false">2678171</guid>        </item>
        <item>
            <title>In vivo and in vitro effects of sizofiran on the human neutrophils and the serum opsonic activity</title>
            <link>http://www.medworm.com/index.php?rid=2503767&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg332674816702517%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In this paper, we examine the effects of SPG, which is a well known BRM, both in vivo and in vitro on the neutrophilic ROS
 production and the serum opsonic activity by the chemiluminescence technique using luminol as a probe.
 
 To investigate the in vivo effects, SPG was administered to 12 healthy male volunteers and two phases of enhancement of the
 neutrophilic ROS production and the serum opsonic activity were observed. In vitro, the addition of SPG showed a dose-dependent
 suppression. To investigate the mechanisms in these contradictory effects of SPG, supernatants of a lymphocytes culture medium
 in the presence of SPG with or without mitogen were added to the neutrophils. The addition of supernatants at a lower concentration
 of SPG (0.01 mg/ml) with mitogens s...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503767</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:38 +0100</pubDate>
            <guid isPermaLink="false">2503767</guid>        </item>
        <item>
            <title>Treatment-induced antibodies to interleukin-2</title>
            <link>http://www.medworm.com/index.php?rid=2503766&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F92346704321p28lu%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Interleukin-2 (IL-2) is a 15 kDa glycoprotein with proven activity as an immune stimulant in the treatment of malignant disorders,
 congenital and acquired immune deficiencies, infectious disorders, and as an adjuvant to vaccines. Both natural and recombinant
 type IL-2 preparations have been applied in clinical treatment trials and have turned out to be immunogenic, although to a
 varying extent. Enzyme immunoassays and western blotting are standard procedures for the detection of IL-2-binding antibodies,
 whereas the neutralizing capacity of these antibodies is frequently demonstrated by inhibition of IL-2-dependent cell growth
 in vitro. The rate of treatment-induced IL-2 antibodies has varied from 0% to 100% in reported trials and frequently exceeded
 50% in patient...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503766</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:38 +0100</pubDate>
            <guid isPermaLink="false">2503766</guid>        </item>
        <item>
            <title>The incidence and clinical significance of antibodies to interferon-a in patients with solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=778842&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq8805302183208x7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It is well known that natural and recombinant proteins can cause antibody formation in the host. We have studied the incidence
 of binding and neutralizing antibodies in carcinoid patients (n=327). All together 204 patients received interferon-α 2b (Intron-A),
 median does 15 MU range 9–35 MU/week subcutaneously and 51% of the patients developed binding antibodies by immunoassay and
 17% showed positive neutralization assay but high titer antibodies (&amp;gt;800 NU/ml) were only found in 4% of the patients. The
 median time until the development of binding antibodies was 26 months and neutralizing antibodies 25 months. Twenty-nine patients
 received interferon-α 2a (Roferon), median does 18 MU/week subcutaneously and 45% developed binding antibodies, 38% had positive
 n...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778842</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:38 +0100</pubDate>
            <guid isPermaLink="false">778842</guid>        </item>
        <item>
            <title>Interferon antibodies in patients with infectious diseases</title>
            <link>http://www.medworm.com/index.php?rid=778841&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1x072774n3u642ul%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Interferons (IFNs) are generally recognized as the most important therapeutic agent in some infectious diseases such as chronic
 hepatitis B and C. Since the early clinical trials it was documented that the therapeutic use of IFNs could be complicated
 by the development of antibodies able to neutralize or to bind to the IFN molecule.
 
 After several years of research it is now widely accepted that the presence of circulating anti-IFN antibodies may affect
 the response to IFN.
 
 
 
 Here we summarize what is currently know on the clinical significance of antibodies to IFN in IFN-treated viral diseases patients.
 
 
	Content TypeJournal Article

	
		JournalBiotherapyOnline ISSN 1573-8280Print ISSN 0921-299X
	
		Journal VolumeVolume 10
	
		Journal IssueVolume 10, Numbe...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778841</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:38 +0100</pubDate>
            <guid isPermaLink="false">778841</guid>        </item>
        <item>
            <title>Natural antibodies to IL-2</title>
            <link>http://www.medworm.com/index.php?rid=778839&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh62j3mvm51p8j7mx%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Natural antibodies to human interleukin-2 are present in sera of patients infected with human immunodeficiency virus and also,
 at a lower titre, in sera of healthy individuals. These antibodies could be purified by affinity-chromatography. Purified
 human anti-hIL-2 antibodies can interfere with lymphocyte proliferation both in the lymphokine activated killer cell assay
 and in the mixed lymphocyte culture. The neutralizing activity observedin vitro suggests that these antibodies play a role in the elaborate cytokine network by which the immune system regulates its response.
 
	Content TypeJournal Article

	
		JournalBiotherapyOnline ISSN 1573-8280Print ISSN 0921-299X
	
		Journal VolumeVolume 10
	
		Journal IssueVolume 10, Number 1 / September, 1997 (Source: Biotherapy...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778839</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:38 +0100</pubDate>
            <guid isPermaLink="false">778839</guid>        </item>
        <item>
            <title>Augumentation of splenic antitumor immunity by local immunotherapy in gastric cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=778853&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy74202l19613n4u7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We previously reported that the antitumor effect of OK-432, a streptococcal preparation, was markedly augmented when this
 agent was injected into tumors together with fibrinogen. In order to elucidate the effect of this treatment on the spleen,
 we assessed splenic function in gastric cancer patients receiving preoperative local immunotherapy with OK-432 and fibrinogen.
 Immunohistochemical studies of the spleen at 7 days after intratumoral injection therapy revealed numerous macrophages phagocytizing
 OK-432 in the splenic sinuses. Phenotypic analysis of splenocytes by flow cytometry revealed an increase in the CD4/CD8 ratio
 and in the expression of HLA-DR, CD25, and Leu M3 by splenic T cells of the patients treated with OK-432 plus fibrinogen when
 compared to patie...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778853</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:37 +0100</pubDate>
            <guid isPermaLink="false">778853</guid>        </item>
        <item>
            <title>The in vitro effect of new muramyl peptide derivatives on cytotoxic activity of NK (Natural Killer) cells from hamsters bearing AB Bomirski Melanoma</title>
            <link>http://www.medworm.com/index.php?rid=778852&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff873r7488t57w531%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The modulation of NK activity by muramyl dipeptides derivatives against Ab (amelanotic) Bomirski melanoma and human erythroleukemia
 K562 cells was studied in vitro. The stimulatory effect was observed for 3 of 7 muramyl dipeptides: MDP(L-Ala)C921, MDPC857
 and L18-MDP(Ala) in relation to cytotoxic activity of NK cells obtained from peripheral blood and spleen of healthy and Ab
 Bomirski melanoma bearing hamsters. An increased of cytotoxic activity NK cells isolated from animals before and during the
 transplantable phase of the tumor against K562 was found. A similar stimulation was received for NK cells obtained from animals
 against their own melanoma cells. The most significant influence of examined MDP derivatives on the cytotoxic activity of
 NK cells were obtaine...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778852</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:37 +0100</pubDate>
            <guid isPermaLink="false">778852</guid>        </item>
        <item>
            <title>Long-term treatment with recombinant interferon alpha-2b prolongs survival of asymptomatic HIV-infected individuals</title>
            <link>http://www.medworm.com/index.php?rid=778843&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F061j1184413n7k77%2F</link>
            <description>Conclusion: IFN alpha treatment given from the early stages of infection, but not after the appearance of AIDS symptoms, can prolong
 survival.
 
 
 
	Content TypeJournal Article

	
		JournalBiotherapyOnline ISSN 1573-8280Print ISSN 0921-299X
	
		Journal VolumeVolume 10
	
		Journal IssueVolume 10, Number 2 / June, 1997 (Source: Biotherapy)</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778843</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:37 +0100</pubDate>
            <guid isPermaLink="false">778843</guid>        </item>
        <item>
            <title>Mpl ligand or thrombopoietin: Biological activities</title>
            <link>http://www.medworm.com/index.php?rid=778837&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm13766w6m48254v4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Thrombopoietin (TPO) or Mpl ligand is the primary physiological regulator of platelet production. This cytokine is the most
 potent stimulator of the proliferation and differentiation of MK progenitor and precursor cellsin vitro. It also acts additively or synergistically with several cytokines on progenitor cells from various hematopoietic lineages,
 including the primitive stem cells. The factor is an extremely potent thrombocytopoietic agent when administrated to normal
 animals, and it accelerates platelet and erythropoietic recovery in several models of myelosuppression. Phase I/II clinical
 trials are ongoing with no detectable adverse effects. Mpl ligand does not induce platelet aggregation, but it lowers the
 platelet sensitivity to physiological dose of agonist...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778837</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:36 +0100</pubDate>
            <guid isPermaLink="false">778837</guid>        </item>
        <item>
            <title>The role of homeobox genes in hematopoiesis</title>
            <link>http://www.medworm.com/index.php?rid=778849&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdwr77u1p412437r5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Homeobox genes encode transcription factors containing a common DNA-binding motif found in virtually all animal species. Different
 homeobox gene families have evolved which encode homeodomains of different types or classes and thus far approximately 170
 homeobox genes have been cloned. Homeoproteins are involved in the control of animal development and several lines of evidence
 strongly suggest that they may contribute to the regulation of hematopoiesis. Many members of this large family are expressed
 in blood cells. Moreover, homeobox containing genes have been involved in translocation events occurring in certain leukemias
 and lymphomas. Furthermore a number of studies indicate that modulation of homeobox gene expression may induce alterations
 in proliferative, ...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778849</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:35 +0100</pubDate>
            <guid isPermaLink="false">778849</guid>        </item>
        <item>
            <title>Foreword</title>
            <link>http://www.medworm.com/index.php?rid=778846&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5n018g26213645x6%2F</link>
            <description>Content TypeJournal Article

	
		JournalBiotherapyOnline ISSN 1573-8280Print ISSN 0921-299X
	
		Journal VolumeVolume 10
	
		Journal IssueVolume 10, Number 4 / December, 1998 (Source: Biotherapy)</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778846</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:35 +0100</pubDate>
            <guid isPermaLink="false">778846</guid>        </item>
        <item>
            <title>Natural and therapeutically-induced antibodies to cytokines</title>
            <link>http://www.medworm.com/index.php?rid=778844&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flw92502743g32454%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Serum samples obtained from non-immunocompromised patients treated therapeutically with recombinant cytokines (e.g. Il-1α; Il-1β; Il-2 to Il-18; IFNα; GM-CSF; G-CSF; etc.) often reveal the presence of high affinity anti-cytokine antibodies. Antibody Fab binding in a saturable
 manner by ELISA and RIA or western immunoblotting prove their specificity. Antibody level often increases in these patients
 with repeated cytokine administration, suggesting boosts of antigen stimulation. However, the appearance in circulation of
 auto-antibodies to exogenous cytokine is not always associated with a decreased clinical response to therapy. The demonstration
 that non-neutralizing auto-antibodies to several natural cytokines can be found even in sera of normal healthy individual...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778844</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:35 +0100</pubDate>
            <guid isPermaLink="false">778844</guid>        </item>
        <item>
            <title>Hematopoietic growth factors in autologous transplantation</title>
            <link>http://www.medworm.com/index.php?rid=778835&amp;cid=s_35911_61_f&amp;fid=35911&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv40w7v17j1831578%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hematopoietic growth factors (HGFs) sustain the survival, proliferation and differentiation of hematopoietic stem cells and
 some functions of mature blood cells. In man several HGFs have been characterised and cloned so far, and this has allowed
 investigators to confer the rationale for the clinical application of these molecules in hematology and oncology. In particular
 G-CSF and GM-CSF are currently utilised to abrogate the hematological toxicity of chemotherapy for standard and dose-intensified
 therapy, neutropenia following bone marrow and peripheral blood stem cell transplantation. Moreover there has recently been
 great interest in the ex vivo expansion of hematopoietic stem and progenitor cells for a variety of applications, such as
 in vitro tumor cell purgi...</description>
            <author>Biotherapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=778835</comments>
            <pubDate>Thu, 19 Jul 2007 07:21:35 +0100</pubDate>
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