Control of MHC restriction by TCR V-alpha CDR1 and CDR2

被引:143
作者
Sim, BC
Zerva, L
Greene, MI
Gascoigne, NRJ
机构
[1] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
[2] UNIV PENN, DEPT PATHOL, PHILADELPHIA, PA 19104 USA
关键词
D O I
10.1126/science.273.5277.963
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Individual T cell receptor (TCR) V-alpha elements are expressed preferentially in CD4 or CD8 peripheral T cell subsets. The closely related V(alpha)3.1 and V(alpha)3.2 elements show reciprocal selection into CD4 and CD8 subsets, respectively. Transgenic mice expressing site-directed mutants of a V alpha 3.1 gene were used to show that individual residues in either the complementarity-determining region 1 (CDR1) or CDR2 were sufficient to change selection from the CD4 subset to the CD8 subset. Thus, the germline-encoded V-alpha elements are a major influence on major histocompatibility class complex (MHC) restriction, most likely by a preferential interaction with one or the other class of MHC molecule.
引用
收藏
页码:963 / 966
页数:4
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