Alanio Cécile, Barreira da Silva Rosa, Michonneau David, Bousso Philippe, Ingersoll Molly A, Albert Matthew L
Laboratory of Dendritic Cell Immunology, Institut Pasteur, 75015 Paris, France.
Inserm U1223, 75015 Paris, France.
J Immunol. 2018 Jan 1;200(1):139-146. doi: 10.4049/jimmunol.1700564. Epub 2017 Nov 29.
The preimmune repertoire consists of mature T lymphocytes that have not yet been stimulated in the periphery. Memory phenotype (MP) cells have been reported as part of the preimmune repertoire (i.e., T cells bearing memory markers despite lack of engagement with cognate Ag); however, little is known about their trafficking and function. In this study, we hypothesized that MP cells, naive to TCR stimulation, constitute a transient population that traffics to tissues during development. Using mutant and transgenic animals with a monospecific TCR, we discovered increased numbers of MP CD8 T cells circulating in nonimmunized and mice compared with wild-type animals. Phenotypic differences included decreased numbers of preimmune MP Ag-specific T cells in the skin and thymus and a distinct pattern of activation upon TCR engagement. Our results show for the first time, to our knowledge, an important role for CXCR3 and CXCL10 in the tissue distribution of preimmune MP cells.
免疫前库由尚未在外周受到刺激的成熟T淋巴细胞组成。记忆表型(MP)细胞已被报道为免疫前库的一部分(即尽管未与同源抗原接触,但带有记忆标记的T细胞);然而,对其迁移和功能知之甚少。在本研究中,我们假设对TCR刺激无反应的MP细胞构成了一个在发育过程中迁移到组织的短暂群体。使用具有单特异性TCR的突变和转基因动物,我们发现与野生型动物相比,未免疫的小鼠和[此处原文缺失相关描述]中循环的MP CD8 T细胞数量增加。表型差异包括皮肤和胸腺中免疫前MP抗原特异性T细胞数量减少以及TCR激活后独特的激活模式。据我们所知,我们的结果首次表明CXCR3和CXCL10在免疫前MP细胞的组织分布中起重要作用。