Institute for Immunology, Biomedical Center Munich (BMC), Ludwig Maximilians Universität, Planegg-Martinsried, Germany.
Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California Berkeley, Berkeley, CA, USA.
Nat Rev Immunol. 2019 Jan;19(1):7-18. doi: 10.1038/s41577-018-0083-6.
The diversion of MHC class II-restricted thymocytes into the regulatory T (T) cell lineage is driven by intrathymic encounter of agonist self-antigens in a similar manner to the clonal deletion of thymocytes. Somewhat paradoxically, it thus seems that the expression of an autoreactive T cell receptor is a shared characteristic of T cells that are subject to clonal deletion and T cells that are diverted into the T cell lineage. Here, we discuss how thymocyte-intrinsic and thymocyte-extrinsic determinants may specify the choice between these two fundamentally different T cell fates.
MHC Ⅱ类限制性胸腺细胞向调节性 T(Treg)细胞谱系的分化是由胸腺内与自身抗原的激动剂相互作用驱动的,其方式类似于胸腺细胞的克隆删除。有些矛盾的是,因此似乎表达自身反应性 T 细胞受体是受克隆删除和转向 T 细胞谱系的 T 细胞的共同特征。在这里,我们讨论了胸腺细胞内在和胸腺细胞外在决定因素如何决定这两种截然不同的 T 细胞命运之间的选择。