Th17 Cells Express Interleukin-10 Receptor and Are Controlled by Foxp3⁻ and Foxp3⁺ Regulatory CD4⁺ T Cells in an Interleukin-10-Dependent Manner

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• 作者：Samuel Huber¹ ; ³ ; ¹¹ ; Nicola Gagliani⁴ ; ⁵ ; ¹¹ ; Enric Esplugues¹ ; ⁶ ; ⁷ ; ¹¹ ; William O'Connor Jr.¹ ; Francis  ; J. Huber¹ ; Ashutosh Chaudhry⁸ ; Masahito Kamanaka¹ ; Yasushi Kobayashi¹ ; Carmen  ; J. Booth² ; Alexander  ; Y. Rudensky⁸ ; Maria  ; Grazia Roncarolo⁵ ; ⁹ ; Manuela Battaglia⁴ ; Richard  ; A. Flavell¹ ; ¹⁰ ; ^{richard.flavell@yale.edu"" rel=""nofollow}
• 刊名：Immunity
• 出版年：2011
• 出版时间：22 April 2011
• 年：2011
• 卷：34
• 期：4
• 页码：554-565
• 全文大小：1904 K

文摘

Summary

T helper 17 (Th17) cells are important for host defense against extracellular microorganisms. However, they are also implicated in autoimmune and chronic inflammatory diseases, and as such need to be tightly regulated. The mechanisms that directly control committed pathogenic Th17 cells in vivo remain unclear. We showed here that IL-17A-producing CD4⁺ T cells expressed interleukin-10 receptor α (IL-10Rα) in vivo. Importantly, T cell-specific blockade of IL-10 signaling led to a selective increase of IL-17A⁺IFN-γ⁻ (Th17) and IL-17A⁺IFN-γ⁺ (Th17+Th1) CD4⁺ T cells during intestinal inflammation in the small intestine. CD4⁺Foxp3⁻ IL-10-producing (Tr1) cells and CD4⁺Foxp3⁺ regulatory (Treg) cells were able to control Th17 and Th17+Th1 cells in an IL-10-dependent manner in vivo. Lastly, IL-10 treatment of mice with established colitis decreased Th17 and Th17+Th1 cell frequencies via direct signaling in T cells. Thus, IL-10 signaling directly suppresses Th17 and Th17+Th1 cells.