超抗原
CD8型
细胞毒性T细胞
肠毒素
T细胞
生物
免疫学
CD28
分子生物学
抗原
细胞生物学
免疫系统
生物化学
基因
体外
大肠杆菌
作者
Chikara Takahashi,Robert S. Mittler,Anthony T. Vella
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1999-05-01
卷期号:162 (9): 5037-5040
被引量:378
标识
DOI:10.4049/jimmunol.162.9.5037
摘要
Abstract After recognition of Ag/MHC and ligation of a costimulatory molecule, resting T cells will clonally expand and then delete to very low levels. Previously, it was shown that deletion can be prevented by coinjection of cytokines or proinflammatory agents such as adjuvants. Here, we demonstrate that ligation of 4-1BB blocks deletion of superantigen-activated T cells in the absence of adjuvant or additional cytokine treatment. Nearly 10 times as many staphylococcal enterotoxin A-specific T cells were detected in the spleens of mice injected 21 days previously with staphylococcal enterotoxin A and an agonist anti-4-1BB Ab compared with mice given staphylococcal enterotoxin A and a control IgG. Even though both CD4- and CD8-activated T cells expressed 4-1BB, a higher proportion of CD8 T cells were rescued compared CD4 T cells. These data suggest that although 4-1BB provides costimulation, it may also promote long-term T cell survival.
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