Positive selection of an H2-M3 restricted T cell receptor

被引:38
作者
Berg, RE
Princiotta, MF
Irion, S
Moticka, JA
Dahl, KR
Staerz, UD [1 ]
机构
[1] Natl Jewish Med & Res Ctr, Dept Med, Denver, CO 80206 USA
[2] Univ Colorado, Hlth Sci Ctr, Ctr Canc, Denver, CO 80220 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80220 USA
关键词
D O I
10.1016/S1074-7613(00)80079-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymocytes are positively selected for alpha beta T cell antigen receptors (TCR) that recognize antigen in conjunction with self-major histocompatibility complex (MHC) molecules. MHC bound peptides participate in positive selection; however, their role has remained controversial. A TCR transgenic mouse was established using a TCR restricted to the MHC class Ib molecule, H2-M3. Having defined H2-M3 as the positively selecting MHC molecule, the severely limited number of H2-M3 binding peptides allowed us to characterize an NADH dehydrogenase subunit 1 (ND1)-derived peptide as the physiological ligand of positive selection. This peptide bears no apparent sequence homology to the cognate peptide, is expressed ubiquitously, and yet does not interfere with peripheral T cells. Our studies also suggest that positive selection becomes promiscuous at high epitope densities.
引用
收藏
页码:33 / 43
页数:11
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