Co-stimulatory members of the TNFR family: Keys to effective T-cell immunity?

被引:740
作者
Croft, M [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Mol Immunol, San Diego, CA 92121 USA
关键词
D O I
10.1038/nri1148
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Interactions between co-stimulatory ligands and their receptors are crucial for the activation of T cells, the prevention of tolerance and the development of T-cell immunity. It is now evident that members of the immunoglobulin-like CD28-B7 co-stimulatory family cannot fully account for an effective long-lasting T-cell response or the generation of memory T cells. Several members of the tumour-necrosis factor receptor (TNFR) superfamily - OX40, 4-1BB, CD27, CD30 and HVEM (herpes-virus entry mediator) - are poised to deliver co-stimulatory signals both early and late after encounter with antigen. The roles of these molecules in initiating and sustaining the T-cell response and in promoting long-lived immunity are discussed.
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页码:609 / 620
页数:12
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