SELECTIVE EXPANSION OF T-CELLS EXPRESSING V-BETA-2 IN TOXIC SHOCK SYNDROME

被引:336
作者
CHOI, YW
LAFFERTY, JA
CLEMENTS, JR
TODD, JK
GELFAND, EW
KAPPLER, J
MARRACK, P
KOTZIN, BL
机构
[1] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT PEDIAT,DIV BASIC SCI,1400 JACKSON ST,DENVER,CO 80206
[2] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT MED,DENVER,CO 80206
[3] NATL JEWISH CTR IMMUNOL & RESP MED,HOWARD HUGHES MED INST,DENVER,CO 80206
[4] UNIV COLORADO,HLTH SCI CTR,DEPT MED,DENVER,CO 80262
[5] UNIV COLORADO,HLTH SCI CTR,DEPT MICROBIOL IMMUNOL,DENVER,CO 80262
[6] UNIV COLORADO,HLTH SCI CTR,DEPT BIOCHEM,DENVER,CO 80262
[7] UNIV COLORADO,HLTH SCI CTR,DEPT BIOPHYS & GENET,DENVER,CO 80262
[8] CHILDRENS HOSP,KEMPE RES CTR,DENVER,CO 80218
关键词
D O I
10.1084/jem.172.3.981
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infection with Staphylococcus aureus and the production of toxic shock syndrome toxin-1 (TSST1) have been implicated in the pathogenesis of toxic shock syndrome. Previous in vitro studies have demonstrated that TSST1 is a powerful but selective stimulator of human T cells, and that the majority of activated cells express the TCR Vβ2 gene segment. We therefore studied patients with toxic shock syndrome using a modification of the PCR to determine if expansion of Vβ2+ T cells is a marker of the in vivo disease process. Five of eight patients studied demonstrated markedly elevated levels of circulating Vβ2+ T cells, whereas none showed significantly elevated levels of T cells expressing other Vβ gene segments. The results suggest that toxin-mediated T cell activation, which involves a large fraction of the human T cell repertoire, may be critical in the pathogenesis of this disease. © 1990, Rockefeller University Press., All rights reserved.
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页码:981 / 984
页数:4
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