抗体
免疫学
重组DNA
免疫球蛋白G
免疫球蛋白E
化学
分子生物学
生物
生物化学
基因
作者
Vincent Hurez,Srini V. Kaveri,Amal Mouhoub,Gilles Dietrich,J C Mani,David Klatzmann,Michel D Kazatchkine
出处
期刊:PubMed
[National Institutes of Health]
日期:1994-10-01
卷期号:1 (5): 269-77
被引量:119
摘要
The effects of intravenously administered normal immunoglobulin G (IVIg) in autoimmune diseases are dependent on the ability of IVIg to interact with surface molecules of lymphocytes. In the present study, we demonstrate the presence of anti-CD4 activity in IVIg by showing the ability of IVIg to bind to CD4 and to inhibit CD4-dependent cellular functions. Binding of IVIg to recombinant soluble human CD4 was assessed by ELISA, immunoblotting and real time analysis of complex formation. Anti-CD4 antibodies isolated from IVIg by affinity-chromatography bound to human CD4+ T cells. These anti-CD4 antibodies inhibited proliferative responses in MLR and infection of CD4+ human T cells with HIV. These results indicate that IVIg contains antibodies reactive with human CD4 and that these anti-CD4 antibodies exhibit biological functions. The presence of anti-CD4 antibodies in IVIg may be relevant to the immunoregulatory effects of normal polyspecific immunoglobulin G.
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