Immune Tolerance Laboratory, Faculty of Medicine, University of New South Wales, Sydney, Australia.
Curr Opin Immunol. 2011 Oct;23(5):641-7. doi: 10.1016/j.coi.2011.07.012. Epub 2011 Aug 11.
Effector T cells have functional subpopulations with distinct cytokine, cytokine receptor, chemokine receptor and transcription factors. We review how activation of antigen specific Treg induces expression of cytokines, cytokine receptors and chemokine receptors depending upon the effector lineage they are activated by. Activated Treg express receptors that are directly related to the effector T cell lineage. Other classes of Treg are induced in the periphery from effector lineage CD4(+)CD25(-)FOXP3(-)CD127(high)T cells, either by IL-10 or TGF-β or by association with activated CD4(+)CD25(+)FOXP3(+)Treg. Thus Treg are produced and adapt to the specific immune inflammatory environment they are activated within. Activated Treg produce different molecules to mediate suppression, which are tailored to the immune response they are activated by and control.
效应 T 细胞具有功能亚群,这些亚群具有不同的细胞因子、细胞因子受体、趋化因子受体和转录因子。我们回顾了抗原特异性 Treg 的激活如何根据其被激活的效应谱系诱导细胞因子、细胞因子受体和趋化因子受体的表达。激活的 Treg 表达与效应 T 细胞谱系直接相关的受体。其他类型的 Treg 在外周从效应谱系 CD4(+)CD25(-)FOXP3(-)CD127(high)T 细胞中被诱导产生,要么通过 IL-10 或 TGF-β,要么通过与激活的 CD4(+)CD25(+)FOXP3(+)Treg 结合。因此,Treg 是在它们被激活的特定免疫炎症环境中产生和适应的。激活的 Treg 产生不同的分子来介导抑制,这些分子针对它们被激活的免疫反应进行了调整和控制。