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葡萄球菌肠毒素A对同种异体刺激的HLA-DQ和DP特异性T细胞的抑制作用。

Inhibition of allostimulated HLA-DQ and DP-specific T cells by staphylococcal enterotoxin A.

作者信息

Masewicz S, Ledbetter J A, Martin P, Mickelson E, Hansen J A, Odum N

机构信息

Human Immunogenetics Program, Fred Hutchinson Cancer Research Center, Seattle, Washington.

出版信息

Hum Immunol. 1993 Mar;36(3):142-8. doi: 10.1016/0198-8859(93)90117-j.

Abstract

Bacterial superantigens have two immunologically important features. They bind MHC class II molecules and stimulate T cells bearing certain V beta TCR phenotypes. Superantigens such as SEA, SEB, and TSST bind to each of the three HLA class II isotypes (DR, DQ, and DP). Allotypic variation seems to play an important role in superantigen binding to class II molecules, but the functional implications of these differences remain largely unknown. In the present investigation, we studied the effects of SEA, SEB, and TSST on allostimulation of HLA-DR-, DQ-, and DP-allospecific T-cell clones. To avoid direct stimulation of T-cell responses by the superantigens, SEA and/or SEB nonresponsive T-cell clones were selected. We show that SEA strongly inhibited DQ- and DP-specific T-cell responses. In contrast, SEB and TSST had only weak inhibitory effects. DR-specific T-cell responses were unaffected or only weakly inhibited by the superantigens tested. The inhibition appeared not to be due to induction of cytotoxicity or suppression of either T cells or EBV-LCLs by SEA. In conclusion, the bacterial superantigen SEA can block alloantigen-specific stimulation of T clones in vitro. These results suggest that SEA binds to certain MHC class II molecules in a way that prevents MHC-TCR interactions.

摘要

细菌超抗原具有两个重要的免疫学特性。它们能结合II类主要组织相容性复合体(MHC)分子,并刺激带有特定VβTCR表型的T细胞。诸如SEA、SEB和TSST等超抗原可与三种HLA II类同种异型分子(DR、DQ和DP)中的每一种结合。同种异型变异似乎在超抗原与II类分子的结合中起重要作用,但这些差异的功能意义仍 largely未知。在本研究中,我们研究了SEA、SEB和TSST对HLA-DR、DQ和DP同种异体特异性T细胞克隆的同种异体刺激作用。为避免超抗原直接刺激T细胞反应,我们选择了对SEA和/或SEB无反应的T细胞克隆。我们发现SEA强烈抑制DQ和DP特异性T细胞反应。相比之下,SEB和TSST的抑制作用较弱。所测试的超抗原对DR特异性T细胞反应无影响或仅有微弱抑制作用。这种抑制作用似乎不是由于SEA诱导细胞毒性或抑制T细胞或EBV-LCLs所致。总之,细菌超抗原SEA在体外可阻断T克隆的同种异体抗原特异性刺激。这些结果表明,SEA以一种阻止MHC-TCR相互作用的方式与某些II类MHC分子结合。

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