The expanding B7 superfamily: Increasing complexity in costimulatory signals regulating T cell function

被引:339
作者
Coyle, AJ [1 ]
Gutierrez-Ramos, JC [1 ]
机构
[1] Millennium PHarmaceut Inc, Inflammat Div, Cambridge, MA 02139 USA
关键词
D O I
10.1038/85251
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Upon encounter with specific antigen, naive T helper precursor (THP) cells become activated,This event is regulated not only by engagement of the T cell receptor (TCR) with peptide presented in the context of major histocompatibility complex (MHC) class II molecules but by a number of costimulatory signals, CD28 engagement by B7-1 and B7-2 on resting THP cells provides a critical signal for initial cell cycle progression, interleukin 2 production and clonal expansion. However, largely as a consequence of the unraveling of the human genome, it is becoming clear that B7-1 and B7-2 are part of a larger family of related counter-receptors that play an essential role in regulating the fate of primed, rather then vesting,THP cells,These molecules play an important sequential role and act, together with B7-1- and B7-2-primed T cells, in the acquisition of effector function and/or tolerance induction.
引用
收藏
页码:203 / 209
页数:7
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