Awasthi Amit, Carrier Yijun, Peron Jean P S, Bettelli Estelle, Kamanaka Masahito, Flavell Richard A, Kuchroo Vijay K, Oukka Mohamed, Weiner Howard L
Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Cambridge, Massachusetts 02139, USA.
Nat Immunol. 2007 Dec;8(12):1380-9. doi: 10.1038/ni1541. Epub 2007 Nov 11.
Regulatory T cells (T(reg) cells) expressing the transcription factor Foxp3 are key in maintaining the balance of immune homeostasis. However, distinct induced T regulatory type 1 (Tr1) cells that lack Foxp3 expression also regulate T cell function, mainly by producing the immunosuppressive cytokine interleukin 10 (IL-10). However, the factors required for the induction of IL-10-producing suppressive T cells are not fully understood. Here we demonstrate that dendritic cells modified by T(reg) cells induced the generation of IL-10-producing Tr1 cells. The differentiation of naive CD4+ T cells into IL-10-producing cells was mediated by IL-27 produced by the T(reg) cell-modified dendritic cells, and transforming growth factor-beta amplified the generation of induced IL-10+ Tr1 cells by IL-27. Thus, IL-27 and transforming growth factor-beta promote the generation of IL-10-producing Tr1 cells.
表达转录因子Foxp3的调节性T细胞(T(reg)细胞)对于维持免疫稳态平衡至关重要。然而,缺乏Foxp3表达的不同诱导性1型调节性T细胞(Tr1细胞)也主要通过产生免疫抑制细胞因子白细胞介素10(IL-10)来调节T细胞功能。然而,诱导产生IL-10的抑制性T细胞所需的因素尚未完全明确。在此,我们证明经T(reg)细胞修饰的树突状细胞可诱导产生IL-10的Tr1细胞的生成。幼稚CD4+ T细胞向产生IL-10细胞的分化由经T(reg)细胞修饰的树突状细胞产生的IL-27介导,而转化生长因子-β通过IL-27放大了诱导性IL-10+ Tr1细胞的生成。因此,IL-27和转化生长因子-β促进了产生IL-10的Tr1细胞的生成。