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CD8 + T细胞对Mls-1a编码的决定簇进行克隆性应答。

CD8+ T cells respond clonally to Mls-1a-encoded determinants.

作者信息

MacDonald H R, Lees R K, Chvatchko Y

机构信息

Ludwig Institute for Cancer Research, Lausanne Branch, Epalinges, Switzerland.

出版信息

J Exp Med. 1990 Apr 1;171(4):1381-6. doi: 10.1084/jem.171.4.1381.

Abstract

T cell responses to the product of the minor lymphocyte stimulatory locus Mls-1a involve the selective use of TCR V beta domains (especially V beta 6 and V beta 8.1) and are generally considered to be restricted to the CD4+ mature subset. We show here that CD8+ (presumably MHC class I-restricted) T cells bearing V beta 6 or V beta 8.1 also respond preferentially to Mls-1a determinants either in vitro (in mixed leukocyte cultures) or in vivo (in an adoptive transfer system). In vitro responses of both CD4+ V beta 6+ and CD8+ V beta 6+ cells to Mls-1a were dependent upon the MHC haplotype of the stimulator cells, with I-E+ (H-2d or H-2k) alleles being much more stimulatory than I-E- (H-2q). These data strengthen the analogy between Mls gene products and other MHC class II-dependent superantigens such as the bacterial enterotoxins.

摘要

T细胞对次要淋巴细胞刺激位点Mls-1a产物的反应涉及TCR Vβ结构域(特别是Vβ6和Vβ8.1)的选择性使用,通常被认为仅限于CD4+成熟亚群。我们在此表明,携带Vβ6或Vβ8.1的CD8+(可能受MHC I类限制)T细胞在体外(混合淋巴细胞培养中)或体内(过继转移系统中)也优先对Mls-1a决定簇作出反应。CD4+ Vβ6+和CD8+ Vβ6+细胞对Mls-1a的体外反应取决于刺激细胞的MHC单倍型,I-E+(H-2d或H-2k)等位基因比I-E-(H-2q)更具刺激作用。这些数据强化了Mls基因产物与其他MHC II类依赖性超抗原(如细菌肠毒素)之间的相似性。

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