Pennock Nathan D, Qian Yamin, Ishihara Kazumi, Nakamura Yamami, Cross Eric, Sakaguchi Shimon, White Jason T
Department of Radiation Medicine, Oregon Health & Science University, Portland, OR 97239, USA.
Department of Experimental Immunology, Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan.
Cell Rep. 2025 Jun 24;44(6):115791. doi: 10.1016/j.celrep.2025.115791. Epub 2025 Jun 6.
Thymic selection predisposes naive T cells to particular outcomes when challenged later with cognate antigen, whether the antigen is self or foreign. This suggests that there is an inherent heterogeneity of functioning among T cells within the naive population (both CD4 and CD8), and that each T cell, as part of its thymic development, is given a certain "programming" that will affect its eventual fate decisions. In this project, we looked at the primary effects of this thymic imprinting on the conversion of naive CD4 T cells into Tregs. Furthermore, using an induced-Treg-reporter system, we examine the impact of thymic imprinted heterogeneity on effector functionality and identity stability. We report that naive T cell differential responsivity to cytokines leads to the observed difference in Treg induction and that the Tregs induced from T cells of different self-affinities maintain a heterogeneity of effector function and identity.
胸腺选择使初始T细胞在随后受到同源抗原(无论该抗原是自身还是外来的)刺激时倾向于特定的结果。这表明在初始群体(CD4和CD8)中的T细胞之间存在功能上的固有异质性,并且每个T细胞作为其胸腺发育的一部分,会被赋予某种“编程”,这将影响其最终的命运决定。在本项目中,我们研究了这种胸腺印记对初始CD4 T细胞转化为调节性T细胞(Tregs)的主要影响。此外,我们使用诱导性Treg报告系统,研究了胸腺印记异质性对效应器功能和身份稳定性的影响。我们报告称,初始T细胞对细胞因子的不同反应性导致了在Treg诱导中观察到的差异,并且从具有不同自身亲和力的T细胞诱导产生的Tregs保持了效应器功能和身份的异质性。