Staton Tracy L, Habtezion Aida, Winslow Monte M, Sato Tohru, Love Paul E, Butcher Eugene C
Program in Immunology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305, USA.
Nat Immunol. 2006 May;7(5):482-8. doi: 10.1038/ni1319. Epub 2006 Apr 2.
Prevailing knowledge dictates that naive alphabeta 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 alphabeta T cell trafficking and suggest that RTEs may be involved in maintaining a diverse immune repertoire at mucosal surfaces.
目前的知识表明,未成熟的αβ T细胞在分化为能够迁移到非淋巴组织的效应T细胞或记忆T细胞之前,需要在淋巴组织中被激活。在此,我们证明CD8(+)近期胸腺迁出细胞(RTEs)可直接迁移至小肠。CCR9、CCL25和α(4)β(7)整合素是CD8(+) RTEs进入肠道所必需的。在T细胞受体受到刺激后,肠道中的CD8(+) RTEs发生增殖,并获得了类似于上皮内淋巴细胞的表面表型。CD8(+) RTEs能够有效地在缺乏淋巴器官的淋巴毒素-α缺陷小鼠的肠道中定植。这些研究对目前关于未成熟αβ T细胞迁移的认识提出了挑战,并表明RTEs可能参与维持黏膜表面多样化的免疫库。