T-CELL RECEPTOR ANTAGONIST PEPTIDES INDUCE POSITIVE SELECTION

被引:2417
作者
HOGQUIST, KA
JAMESON, SC
HEATH, WR
HOWARD, JL
BEVAN, MJ
CARBONE, FR
机构
[1] UNIV WASHINGTON,HOWARD HUGHES MED INST,DEPT IMMUNOL,SEATTLE,WA 98195
[2] ROYAL MELBOURNE HOSP,WALTER & ELIZA HALL INST MED RES,PARKVILLE,VIC 3050,AUSTRALIA
[3] MONASH UNIV,SCH MED,DEPT PATHOL & IMMUNOL,PRAHRAN,VIC 3181,AUSTRALIA
关键词
D O I
10.1016/0092-8674(94)90169-4
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
We have used organ culture of fetal thymic lobes from T cell receptor (TCR) transgenic beta2M(-/-) mice to study the role of peptides in positive selection. The TCR used was from a CD8+ T cell specific for ovalbumin 257-264 in the context of K(b). Several peptides with the ability to induce positive selection were identified. These peptide-selected thymocytes have the same phenotype as mature CD8+ T cells and can respond to antigen. Those peptides with the ability to induce positive selection were all variants of the antigenic peptide and were identified as TCR antagonist peptides for this receptor. One peptide tested, E1, induced positive selection on the beta2M(-/-) background but negative selection on the beta2M(+/-) background. These results show that the process of positive selection is exquisitely peptide specific and sensitive to extremely low ligand density and support the notion that low efficacy ligands mediate positive selection.
引用
收藏
页码:17 / 27
页数:11
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