ON THE COMPLEXITY OF SELF

被引:256
作者
RUDENSKY, AY
RATH, S
PRESTONHURLBURT, P
MURPHY, DB
JANEWAY, CA
机构
[1] YALE UNIV,SCH MED,IMMUNOBIOL SECT,NEW HAVEN,CT 06510
[2] HOWARD HUGHES MED INST,NEW HAVEN,CT 06510
关键词
D O I
10.1038/353660a0
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
SELF peptides bound to self major histocompatibility complex (MHC) molecules have been implicated both in positive 1,2 and in negative 3,4 selection of T cells during intrathymic development. We report here that the novel MHC-restricted monoclonal antibody Y-Ae (ref. 5) detects the MHC class II bound form of a major self peptide 6. Y-Ae binds approximately 12% of the relevant MHC class II molecules on self antigen presenting cells. The peptide detected by Y-Ae is one of several major peptides eluted from the MHC molecule 6. These data suggest that self peptides presented by self MHC class II molecules at densities sufficient to signal a CD4 T cell are of very limited complexity. Furthermore, as Y-Ae stains antigen presenting cells that mediate negative selection but not thymic cortical epithelial cells 5 that drive positive selection 3, differential expression of self peptide:self MHC class II complexes may be a key feature of intrathymic selection.
引用
收藏
页码:660 / 662
页数:3
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