How the T cell repertoire becomes peptide and MHC specific

被引:252
作者
Huseby, ES
White, J
Crawford, F
Vass, T
Becker, D
Pinilla, C
Marrack, P [1 ]
Kappler, JW
机构
[1] Natl Jewish Med & Res Ctr, Howard Hughes Med Inst, Denver, CO 80206 USA
[2] Natl Jewish Med & Res Ctr, Integrated Dept Immunol, Denver, CO 80206 USA
[3] Torrey Pines Inst Mol Studies, San Diego, CA 92121 USA
[4] Univ Colorado, Ctr Hlth Sci, Dept Biochem & Mol Genet, Denver, CO 80206 USA
[5] Univ Colorado, Ctr Hlth Sci, Dept Med, Denver, CO 80206 USA
[6] Univ Colorado, Ctr Hlth Sci, Dept Pharmacol, Denver, CO 80206 USA
关键词
D O I
10.1016/j.cell.2005.05.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T cells bearing up T cell receptors (TCRs) recognize antigens in the form of peptides bound to class I or class II major histocompatibility proteins (MHC). TCRs on mature T cells are usually very specific for both peptide and MHC class and allele. They are picked out from a precursor population in the thymus by MHC-driven positive and negative selection. Here we show that the pool of T cells initially positively selected in the thymus contains many T cells that are very crossreactive for peptide and MHC and that subsequent negative selection establishes the MHC-restriction and peptide specificity of peripheral T cells. Our results also suggest that germline-encoded TCR variable elements have an inherent predisposition to react with features shared by all MHC proteins.
引用
收藏
页码:247 / 260
页数:14
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