Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of TH17 cell immunity

肠道调节性T细胞选择性产生IL-27,从而实现对TH17细胞免疫的肠道特异性调节。

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作者:Chia-Hao Lin ,Cheng-Jang Wu ,Sunglim Cho ,Rasika Patkar ,William J Huth ,Ling-Li Lin ,Mei-Chi Chen ,Elisabeth Israelsson ,Joanne Betts ,Magdalena Niedzielska ,Shefali A Patel ,Han G Duong ,Romana R Gerner ,Chia-Yun Hsu ,Matthew Catley ,Rose A Maciewicz ,Hiutung Chu ,Manuela Raffatellu ,John T Chang ,Li-Fan Lu

Abstract

Regulatory T cells (Treg cells) are instrumental in establishing immunological tolerance. However, the precise effector mechanisms by which Treg cells control a specific type of immune response in a given tissue remains unresolved. By simultaneously studying Treg cells from different tissue origins under systemic autoimmunity, in the present study we show that interleukin (IL)-27 is specifically produced by intestinal Treg cells to regulate helper T17 cell (TH17 cell) immunity. Selectively increased intestinal TH17 cell responses in mice with Treg cell-specific IL-27 ablation led to exacerbated intestinal inflammation and colitis-associated cancer, but also helped protect against enteric bacterial infection. Furthermore, single-cell transcriptomic analysis has identified a CD83+CD62Llo Treg cell subset that is distinct from previously characterized intestinal Treg cell populations as the main IL-27 producers. Collectively, our study uncovers a new Treg cell suppression mechanism crucial for controlling a specific type of immune response in a particular tissue and provides further mechanistic insights into tissue-specific Treg cell-mediated immune regulation.

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