CD8+ recent thymic emigrants home to and efficiently repopulate the small intestine epithelium

被引:87
作者
Staton, TL
Habtezion, A
Winslow, MM
Sato, T
Love, PE
Butcher, EC [1 ]
机构
[1] Stanford Univ, Sch Med, Program Immunol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Lab Immunol & Vasc Biol, Stanford, CA 94305 USA
[3] Vet Affairs Palo Alto Hlth Care Syst, Ctr Mol Biol & Med, Palo Alto, CA 94304 USA
[4] NICHHD, Lab Mammalian Genes & Dev, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1038/ni1319
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Prevailing knowledge dictates that naive ab T cells require activation in lymphoid tissues before differentiating into effector or memory T cells capable of trafficking to nonlymphoid tissues. Here we demonstrate that CD8(+) recent thymic emigrants (RTEs) migrated directly into the small intestine. CCR9, CCL25 and alpha(4)beta(7) integrin were required for gut entry of CD8(+) RTEs. After T cell receptor stimulation, intestinal CD8+ RTEs proliferated and acquired a surface phenotype resembling that of intraepithelial lymphocytes. CD8(+) RTEs efficiently populated the gut of lymphotoxin-alpha-deficient mice, which lack lymphoid organs. These studies challenge the present understanding of naive alpha beta T cell trafficking and suggest that RTEs may be involved in maintaining a diverse immune repertoire at mucosal surfaces.
引用
收藏
页码:482 / 488
页数:7
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