CPTP, Université de Toulouse, CNRS, Inserm, UPS, Toulouse, France.
Protein Cell. 2018 Apr;9(4):322-332. doi: 10.1007/s13238-017-0425-3. Epub 2017 May 24.
Immunosuppressive regulatory T lymphocytes (Treg) expressing the transcription factor Foxp3 play a vital role in the maintenance of tolerance of the immune-system to self and innocuous non-self. Most Treg that are critical for the maintenance of tolerance to self, develop as an independent T-cell lineage from common T cell precursors in the thymus. In this organ, their differentiation requires signals from the T cell receptor for antigen, from co-stimulatory molecules, as well as from cytokine-receptors. Here we focus on the cytokines implicated in thymic development of Treg, with a particular emphasis on the roles of interleukin-2 (IL-2) and IL-15. The more recently appreciated involvement of TGF-β in thymic Treg development is also briefly discussed. Finally, we discuss how cytokine-dependence of Treg development allows for temporal, quantitative, and potentially qualitative modulation of this process.
表达转录因子 Foxp3 的免疫抑制调节性 T 淋巴细胞(Treg)在维持免疫系统对自身和无害非自身的耐受性方面发挥着至关重要的作用。大多数对于维持对自身的耐受性至关重要的 Treg,是从胸腺中的共同 T 细胞前体中独立分化出来的 T 细胞谱系。在这个器官中,它们的分化需要来自抗原的 T 细胞受体、共刺激分子以及细胞因子受体的信号。在这里,我们重点介绍了与 Treg 胸腺发育相关的细胞因子,特别强调了白细胞介素 2(IL-2)和白细胞介素 15(IL-15)的作用。最近发现转化生长因子-β(TGF-β)也参与了胸腺 Treg 的发育,这也将在文中简要讨论。最后,我们讨论了 Treg 发育对细胞因子的依赖性如何允许对该过程进行时间、数量和潜在质量的调节。