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微生物T细胞促细胞分裂剂对MHC I类限制性CD8+细胞毒性T淋巴细胞的激活作用。对靶细胞MHC II类表达及应答T细胞Vβ使用情况的依赖性。

Activation of MHC class I-restricted CD8+ CTL by microbial T cell mitogens. Dependence upon MHC class II expression of the target cells and V beta usage of the responder T cells.

作者信息

Herrmann T, Maryanski J L, Romero P, Fleischer B, MacDonald H R

机构信息

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

出版信息

J Immunol. 1990 Feb 15;144(4):1181-6.

PMID:1968075
Abstract

The T cell response to microbial T cell mitogens (MTM) such as enterotoxins from Staphylococcus aureus (SE) and the soluble mitogen from Mycoplasma arthritidis, resemble the minor lymphocyte stimulatory locus (Mls) response in several aspects. An important feature of the Mls response is it restriction to CD4+ cells. This study demonstrates that in contrast to Mls, the MTM response includes both CD4+ and CD8+ subsets. Both CD4+ and CD8+ cells expanded in IL-2 after stimulation with SEB showed preferential expression of T cell receptors bearing V beta 8 domains. Mouse and human target cells could be lysed in the presence of MTM both by MTM-stimulated CD8+ lymphocytes and by MHC class I-restricted CTL clones of defined Ag specificity. MTM-induced lysis required the expression of MHC class II, but not class I Ag, on the target cells. Inhibition studies of SEB and Ag-dependent cytolysis by CTL clones underlined the crucial role of CD3 and LFA-1 in both instances, but showed CD8 dependence only for AG-dependent cytolysis. Together these findings suggest important differences between the putative MTM-mediated interaction of TCR with MHC molecules and the classical TCR/MHC interaction involved in MHC-restricted Ag recognition.

摘要

T细胞对微生物T细胞促有丝分裂原(MTM)的反应,如金黄色葡萄球菌肠毒素(SE)和关节炎支原体的可溶性促有丝分裂原,在几个方面类似于次要淋巴细胞刺激位点(Mls)反应。Mls反应的一个重要特征是它对CD4 +细胞的限制。本研究表明,与Mls不同,MTM反应包括CD4 +和CD8 +亚群。用SEB刺激后,CD4 +和CD8 +细胞在IL-2中均有扩增,显示出携带Vβ8结构域的T细胞受体的优先表达。MTM刺激的CD8 +淋巴细胞和具有确定抗原特异性的MHC I类限制性CTL克隆均可在MTM存在的情况下裂解小鼠和人类靶细胞。MTM诱导的裂解需要靶细胞上表达MHC II类分子,而不是I类抗原。对SEB和CTL克隆的抗原依赖性细胞溶解的抑制研究强调了CD3和LFA-1在这两种情况下的关键作用,但仅显示CD8对抗原依赖性细胞溶解的依赖性。这些发现共同表明,推测的MTM介导的TCR与MHC分子的相互作用与参与MHC限制性抗原识别的经典TCR / MHC相互作用之间存在重要差异。

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