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将循环自身蛋白(C5)呈递给MHC II类限制性T细胞。

Presentation of a circulating self protein (C5) to MHC class II restricted T cells.

作者信息

Stockinger B, Lin R H, Grant C

机构信息

National Institute for Medical Research, The Ridgeway, Mill Hill, London, England.

出版信息

Int Rev Immunol. 1993;10(4):357-64. doi: 10.3109/08830189309061710.

Abstract

Presentation of a soluble self antigen, the fifth component of complement (C5), is discussed with emphasis on the differential ability of presentation by subpopulations of APC (dendritic cells, macrophages, B cells, fibroblasts, B cell lines and bone marrow macrophages). Constitutive presentation of C5 in C5 sufficient mice is a prerequisite for tolerance induction in MHC class II restricted T cells and can be directly demonstrated by the ability of ex-vivo APC from C5 sufficient, but not C5 deficient mice, to activate C5 specific T cells in vitro in the absence of added antigen. C5 presentation and tolerance induction in MHC class II restricted T cells is strictly dependent on an exogenous source of self antigen. C5 biosynthesized, but not secreted by macrophages is ignored by MHC class II restricted cells and induces neither tolerance nor autoimmunity. C5 presentation for tolerance induction depends largely on the efficiency of antigen uptake by APC, a property which varies within different APC subpopulations and with the nature of the antigen.

摘要

本文讨论了可溶性自身抗原补体第五成分(C5)的呈递,重点关注抗原呈递细胞(树突状细胞、巨噬细胞、B细胞、成纤维细胞、B细胞系和骨髓巨噬细胞)亚群的不同呈递能力。在C5充足的小鼠中,C5的组成性呈递是MHC II类限制性T细胞诱导耐受的先决条件,并且可以通过来自C5充足但非C5缺陷小鼠的体外抗原呈递细胞在无添加抗原的情况下体外激活C5特异性T细胞的能力直接证明。MHC II类限制性T细胞中的C5呈递和耐受诱导严格依赖于自身抗原的外源性来源。巨噬细胞生物合成但未分泌的C5被MHC II类限制性细胞忽略,既不诱导耐受也不诱导自身免疫。用于耐受诱导的C5呈递很大程度上取决于抗原呈递细胞摄取抗原的效率,这一特性在不同的抗原呈递细胞亚群中以及随抗原的性质而变化。

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