Wang Baomei, Primeau Tina M, Myers Nancy, Rohrs Henry W, Gross Michael L, Lybarger Lonnie, Hansen Ted H, Connolly Janet M
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Science. 2009 Nov 6;326(5954):871-4. doi: 10.1126/science.1177627.
Pathogen recognition by T cells is dependent on their exquisite specificity for self-major histocompatibility complex (MHC) molecules presenting a bound peptide. Although this specificity results from positive and negative selection of developing T cells in the thymus, the relative contribution of these two processes remains controversial. To address the relation between the selecting peptide-MHC complex and the specificity of mature T cells, we generated transgenic mice that express a single peptide-MHC class I complex. We demonstrate that positive selection of CD8 T cells in these mice results in an MHC-specific repertoire. Although selection on a single complex is peptide promiscuous, mature T cells are highly peptide specific. Thus, positive selection imparts MHC and peptide specificity on the peripheral CD8 T cell repertoire.
T细胞对病原体的识别依赖于它们对呈递结合肽的自身主要组织相容性复合体(MHC)分子的高度特异性。尽管这种特异性源于胸腺中发育中的T细胞的阳性和阴性选择,但这两个过程的相对贡献仍存在争议。为了研究选择肽-MHC复合体与成熟T细胞特异性之间的关系,我们构建了表达单一肽-MHC I类复合体的转基因小鼠。我们证明,这些小鼠中CD8 T细胞的阳性选择导致了MHC特异性库的形成。尽管在单一复合体上的选择对肽具有混杂性,但成熟T细胞对肽具有高度特异性。因此,阳性选择赋予外周CD8 T细胞库MHC和肽的特异性。