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细胞表面识别结构在T细胞启动MHC非限制性“混杂”杀伤中的作用。

The role of cell surface recognition structures in the initiation of MHC-unrestricted 'promiscuous' killing by T cells.

作者信息

Thiele D L, Lipsky P E

出版信息

Immunol Today. 1989 Nov;10(11):375-81. doi: 10.1016/0167-5699(89)90271-5.

Abstract

CD3+ T cells mediate relatively promiscuous patterns of major histocompatibility complex (MHC)-unrestricted target cell lysis following activation. Cell-cell contact between target and effector cells is essential in this form of cytotoxicity. Although the T-cell receptor (TCR)-CD3 molecular complex can transmit signals that initiate MHC unrestricted T-cell killing, recognition of targets by the TCR is not essential for this form of cytotoxicity. In this review by Dwain Thiele and Peter Lipsky, a model of the triggering of T cells to effect MHC-unrestricted cytotoxicity is proposed.

摘要

CD3 + T细胞活化后介导相对混杂的主要组织相容性复合体(MHC)非限制性靶细胞裂解模式。靶细胞与效应细胞之间的细胞间接触在这种细胞毒性形式中至关重要。尽管T细胞受体(TCR)-CD3分子复合物可以传递启动MHC非限制性T细胞杀伤的信号,但TCR对靶标的识别对于这种细胞毒性形式并非必不可少。在德韦恩·蒂勒(Dwain Thiele)和彼得·利普斯基(Peter Lipsky)撰写的这篇综述中,提出了一种T细胞触发以实现MHC非限制性细胞毒性的模型。

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