CD28-B7 INTERACTIONS IN T-CELL ACTIVATION

被引:300
作者
ALLISON, JP [1 ]
机构
[1] UNIV CALIF BERKELEY,CANC RES LAB,BERKELEY,CA 94720
关键词
D O I
10.1016/0952-7915(94)90120-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous work has shown that optimal activation of CD4(+) T cells requires co-stimulatory signals in addition to the primary signal provided by the antigen receptor. Recent work has demonstrated that CD28 is the primary co-stimulatory signal receptor for T cells, and B7 its natural ligand on antigen presenting cells. In the past year, it has become clear that the importance of CD28-mediated co-stimulatory signals extends to virtually all T-cell subsets. In addition, the existence of multiple ligands that are differentially expressed on antigen-presenting cells has been documented. The picture that is emerging is of a complex and dynamic interplay of co-stimulatory molecules on both the T cell and the antigen-presenting cell that serves to regulate activation. This offers novel approaches to the manipulation of immune responses in vivo.
引用
收藏
页码:414 / 419
页数:6
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