Co-inhibitory molecules of the B7-CD28 family in the control of T-cell immunity

被引:1077
作者
Chen, LP [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21287 USA
关键词
D O I
10.1038/nri1349
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Co-signalling molecules are cell-surface glycoproteins that can direct, modulate and fine-tune T-cell receptor (TCR) signals. On the basis of their functional outcome, co-signalling molecules can be divided into co-stimulators and co-inhibitors, which promote or suppress T-cell activation, respectively. By expression at the appropriate time and location, co-signalling molecules positively and negatively control the priming, growth, differentiation and functional maturation of a T-cell response. We are now beginning to understand the power of co-inhibitors in the context of lymphocyte homeostasis and the pathogenesis of human diseases. In this article, I focus on several newly described co-inhibitory pathways in the B7-CD28 family.
引用
收藏
页码:336 / 347
页数:12
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