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蛋白酶抑制剂对克隆化T细胞抗原呈递的选择性抑制作用。

Selective inhibition of antigen presentation to cloned T cells by protease inhibitors.

作者信息

Puri J, Factorovich Y

机构信息

Department of Chemical Immunology, Weizmann Institute of Sciences, Rehovot, Israel.

出版信息

J Immunol. 1988 Nov 15;141(10):3313-7.

PMID:3263420
Abstract

The effect of eight microbial protease inhibitors on Ag-presentation to six different Ag-specific T cell clones was investigated. We found that these protease inhibitors can inhibit Ag presentation in a highly selective manner. This selectivity was evident with T cell clones specific to different Ag as well as with T cells specific to the same Ag but differing in their H-2 restriction. The inhibition was to due to cytotoxicity or effects through the TCR because none of the eight inhibitors inhibited IL-2-induced T cell proliferation, and because they did not inhibit Ag presentation by fixed APC or synthetic polypeptide. The conclusion after these data suggests that each specific antigenic fragment is produced by a unique set of proteases.

摘要

研究了八种微生物蛋白酶抑制剂对六种不同抗原特异性T细胞克隆的抗原呈递的影响。我们发现这些蛋白酶抑制剂能够以高度选择性的方式抑制抗原呈递。这种选择性在针对不同抗原的T细胞克隆以及针对相同抗原但H-2限制不同的T细胞中都很明显。这种抑制不是由于细胞毒性或通过TCR的作用,因为这八种抑制剂都没有抑制IL-2诱导的T细胞增殖,并且它们也没有抑制固定抗原呈递细胞或合成多肽的抗原呈递。这些数据得出的结论表明,每个特定的抗原片段都是由一组独特的蛋白酶产生的。

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