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对I-E分子上功能性T细胞识别位点的分析。

An analysis of functional T cell recognition sites on I-E molecules.

作者信息

Needleman B W, Pierres M, Devaux C A, Dwyer P N, Finnegan A, Sachs D H, Hodes R J

出版信息

J Immunol. 1984 Aug;133(2):589-96.

PMID:6203968
Abstract

The recognition of I-E molecules by antigen-specific T cells was studied to determine if one or multiple topographic sites on the I-E molecules can function as restricting elements for T cells. A panel of 14 I-Ek-specific monoclonal antibodies (mAb) was used to inhibit T cell proliferation induced by antigens, the recognition of which was restricted by I-E-encoded determinants. These antibodies gave patterns of inhibition that were similar for three long-term antigen-specific T cell lines. Multiple distinct patterns of inhibition, however, were observed when a series of antigen-specific I-E-restricted T cell clones was studied. Differences were identified even among clones expressing apparently similar antigen specificities and MHC restriction. The observed inhibition by these antibodies appeared to be caused by specific steric or allosteric interference with T cell recognition of antigen and Ia. Based on the differences in patterns of inhibition, it was possible to infer the existence of distinct sites or conformations on the I-E molecule that are functionally involved in antigen-specific T cell recognition.

摘要

研究了抗原特异性T细胞对I-E分子的识别,以确定I-E分子上的一个或多个拓扑位点是否可作为T细胞的限制元件。使用一组14种I-Ek特异性单克隆抗体(mAb)来抑制由抗原诱导的T细胞增殖,这些抗原的识别受I-E编码的决定簇限制。对于三个长期抗原特异性T细胞系,这些抗体给出的抑制模式相似。然而,当研究一系列抗原特异性I-E限制的T细胞克隆时,观察到多种不同的抑制模式。即使在表达明显相似的抗原特异性和MHC限制的克隆之间也发现了差异。这些抗体观察到的抑制作用似乎是由对T细胞对抗原和Ia的识别的特异性空间或别构干扰引起的。基于抑制模式的差异,可以推断I-E分子上存在在功能上参与抗原特异性T细胞识别的不同位点或构象。

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