Suppr超能文献

细胞毒性T淋巴细胞针对同种异体抗原产生过程中T-T相互作用的多种途径。

Multiple pathways of T-T interaction in the generation of cytotoxic T lymphocytes to alloantigens.

作者信息

Corley R B, Switzer K A, Hudson D E, Cooley M A

出版信息

J Exp Med. 1980 May 1;151(5):1125-38. doi: 10.1084/jem.151.5.1125.

Abstract

The interaction of T helper (Th) cells with syngeneic and allogeneic cytotoxic T lymphocyte precursors (CTL.P) has been investigated. Unprimed and mixed lymphocyte culture-primed peripheral T cells were used as a source of Th. Thymocytes, which depend upon exogenous Th cells for activation, were used as a source of cytotoxic precursors. Data is presented that demonstrates that at least two pathways of T-T interaction can lead to the activation of cytotoxic lymphocytes. The first is an allogeneic effect, in which Th cells recognize and respond to alloantigens expressed on CTL.P. The second is the interaction of Th cells with syngeneic CTL.P, in which both cell types are thought to respond to alloantigens on stimulator cells. The latter interaction can be shown to be restricted by H-2-linked determinants when primed Th cells are used and allogeneic effects against thymocytes are minimized. Restricted interactions between unprimed Th cells and thymocyte CTL.P have never been observed. Mechanisms that may explain the difference between the interaction of unprimed and primed Th cells with CTL.P are discussed.

摘要

已对辅助性T(Th)细胞与同基因和异基因细胞毒性T淋巴细胞前体(CTL.P)之间的相互作用进行了研究。未致敏的和经混合淋巴细胞培养致敏的外周T细胞被用作Th细胞的来源。依赖外源性Th细胞激活的胸腺细胞被用作细胞毒性前体的来源。所呈现的数据表明,至少两条T细胞与T细胞相互作用的途径可导致细胞毒性淋巴细胞的激活。第一条是异基因效应,其中Th细胞识别并响应CTL.P上表达的同种异体抗原。第二条是Th细胞与同基因CTL.P的相互作用,其中两种细胞类型都被认为对刺激细胞上的同种异体抗原作出反应。当使用致敏的Th细胞且对胸腺细胞的异基因效应最小化时,后一种相互作用可显示受H-2连锁决定簇的限制。从未观察到未致敏的Th细胞与胸腺细胞CTL.P之间的限制性相互作用。讨论了可能解释未致敏和致敏的Th细胞与CTL.P相互作用差异的机制。

相似文献

本文引用的文献

9
Induction of secondary cytotoxic T-lymphocytes in vitro does not require cell proliferation.
Proc Soc Exp Biol Med. 1976 Feb;151(2):348-50. doi: 10.3181/00379727-151-39207.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验