Inhibition of thymocyte positive selection by natural MHC: peptide ligands

被引:0
|
作者
Tourne, S
Kouskoff, V
Ho, W
Davis, M
Benoist, C
Mathis, D
机构
[1] IGMBC, CNRS, INSERM, ULP, F-67404 Illkirch Graffenstaden, France
[2] Stanford Univ, Sch Med, Beckman Ctr, HHMI Res Labs, Stanford, CA 94305 USA
关键词
T cell differentiation; TCR transgenic mouse; antagonism; invariant chain;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The 3A9 transgenic mouse line carries the rearranged TCR genes from a T cell hybridoma that recognizes hen egg lysozyme peptide 46-61 in the context of MHC class II A(k) molecules. As expected, positive selection of immature 3A9 thymocytes to become mature CD4(+) 8(-) T cells was efficient on the "selecting" CBA (H-2(k)) genetic background but not on the "non-selecting" C57BL/6 (H-2(b)) background. Surprisingly, positive selection was also inefficient on the CBA x C57BL/6 F1 background (H-2(kb)). We present evidence that expression of A(beta)(b) molecules on thymus epithelium (in conjunction with A(alpha)(b) or A(u)(k) molecules) inhibits the positive selection of 3A9 thymocytes mediated by A(alpha)(k):A(beta)(k) complexes, in a process evocative of peptide antagonism of mature T cells.
引用
收藏
页码:394 / 402
页数:9
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