Fuller B, Lefrançois L
Division of Rheumatic Diseases, University of Connecticut Health Center, Farmington 06030, USA.
J Immunol. 1995 Sep 15;155(6):2808-11.
We have examined whether the thymus can produce immature T cell precursors for subsequent positive selection in the periphery. Using the intestine as a model system, we demonstrate that extrathymic MHC class I molecules positively select thymus-derived TCR-alpha beta CD8+ intestinal intraepithelial lymphocytes. Grafting of MHC class I+ thymus onto MHC class I- hosts resulted in the generation of donor and host-derived CD4-CD8+ T cells in lymph node, but few TCR-alpha beta CD4-CD8+ intraepithelial lymphocytes. The results indicate that the intestine can act as a site of positive selection for thymus-derived T cells. Bone marrow reconstitution studies demonstrated that non-hematopoietic, radiation-resistant cells, perhaps intestinal epithelial cells, were responsible for extrathymic positive selection of thymus-derived T cells. These findings demonstrate that the thymus can support organ-specific immunity via provision of targeted precursor populations.
我们研究了胸腺是否能产生未成熟的T细胞前体,以便在周围组织中进行后续的阳性选择。以肠道作为模型系统,我们证明胸腺外的MHC I类分子可对源自胸腺的TCR-αβ CD8+肠道上皮内淋巴细胞进行阳性选择。将MHC I类阳性胸腺移植到MHC I类阴性宿主上,导致在淋巴结中产生供体和宿主来源的CD4-CD8+ T细胞,但TCR-αβ CD4-CD8+上皮内淋巴细胞很少。结果表明,肠道可作为源自胸腺的T细胞进行阳性选择的场所。骨髓重建研究表明,非造血、抗辐射细胞,可能是肠道上皮细胞,负责对源自胸腺的T细胞进行胸腺外阳性选择。这些发现表明,胸腺可通过提供靶向性前体细胞群来支持器官特异性免疫。