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用于实验性自身免疫疾病免疫治疗的MHC结合肽

MHC-binding peptides for immunotherapy of experimental autoimmune disease.

作者信息

Wraith D C, Smilek D E, Webb S

机构信息

Division of Immunology, Cambridge University Department of Pathology, UK.

出版信息

J Autoimmun. 1992 Apr;5 Suppl A:103-13. doi: 10.1016/0896-8411(92)90025-l.

Abstract

It is now well accepted that T helper cells play a central role in the induction and maintenance of autoimmune disease. Many experimental models have emphasized this fact and have illustrated the efficacy of therapeutic strategies aimed at disrupting T cell recognition of autoantigens. Antibodies directed at either class II proteins of the major histocompatibility complex (MHC) or CD4 accessory molecules have been universally successful. However, the potential use of antibodies for therapy in humans is complicated by host anti-globulin and anti-idiotype responses. An alternative approach to anti-MHC blockade with antibodies is peptide blockade of MHC molecules. In addition, peptides may be used as agonists of autoantigens in order to modulate the autoimmune response. The use of synthetic peptides for therapy is an innovative yet relatively unexplored approach and will be the subject for discussion in this article.

摘要

现在人们普遍认为,辅助性T细胞在自身免疫性疾病的诱发和维持中起着核心作用。许多实验模型都强调了这一事实,并说明了旨在破坏T细胞对自身抗原识别的治疗策略的有效性。针对主要组织相容性复合体(MHC)的II类蛋白或CD4辅助分子的抗体一直都很成功。然而,抗体在人类治疗中的潜在应用因宿主抗球蛋白和抗独特型反应而变得复杂。用抗体进行抗MHC阻断的一种替代方法是肽对MHC分子的阻断。此外,肽可作为自身抗原的激动剂,以调节自身免疫反应。使用合成肽进行治疗是一种创新但相对未被探索的方法,将是本文讨论的主题。

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