HUMAN B7-1 (CD80) AND B7-2 (CD86) BIND WITH SIMILAR AVIDITIES BUT DISTINCT KINETICS TO CD28 AND CTLA-4 RECEPTORS

被引:838
作者
LINSLEY, PS
GREENE, JL
BRADY, W
BAJORATH, J
LEDBETTER, JA
PEACH, R
机构
[1] Bristol-Myers Squibb, Pharmaceutical Research Institute, Seattle, WA 98121
关键词
D O I
10.1016/S1074-7613(94)80021-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B7-0 or B7-2 (CD86) is a T cell costimulatory molecule that binds the same receptors (CD28 and CTLA-4) as B7-1 (CD80), but shares with it only similar to 25% sequence identity and is expressed earlier during an immune response. Here we show that human CD86 maintains similar (within similar to 2- to 3-fold) overall receptor binding and T cell costimulatory properties as CD80. However, CD80 and CD86 did not bind equivalently to CTLA-4: CD80 bound Y100A, a form of CTLA4lg with a mutation in the CDR3-like region, >200-fold better than did CD86; inhibition of CD80-mediated cellular responses required similar to 100-fold lower CTLA4lg concentrations; and CD80-CTLA4lg complexes dissociated 5- to 8-fold more slowly. Thus, CD80 and CD86 utilize different binding determinants and have different kinetics of binding to CD28 and CTLA-4.
引用
收藏
页码:793 / 801
页数:9
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