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Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity.
Lin, Chia-Hao; Wu, Cheng-Jang; Cho, Sunglim; Patkar, Rasika; Lin, Ling-Li; Chen, Mei-Chi; Israelsson, Elisabeth; Betts, Joanne; Niedzielska, Magdalena; Patel, Shefali A; Duong, Han G; Gerner, Romana R; Hsu, Chia-Yun; Catley, Matthew; Maciewicz, Rose A; Chu, Hiutung; Raffatellu, Manuela; Chang, John T; Lu, Li-Fan.
Afiliação
  • Lin CH; School of Biological Sciences, University of California, San Diego, La Jolla, California , CA, USA.
  • Wu CJ; School of Biological Sciences, University of California, San Diego, La Jolla, California , CA, USA.
  • Cho S; School of Biological Sciences, University of California, San Diego, La Jolla, California , CA, USA.
  • Patkar R; School of Biological Sciences, University of California, San Diego, La Jolla, California , CA, USA.
  • Lin LL; School of Biological Sciences, University of California, San Diego, La Jolla, California , CA, USA.
  • Chen MC; School of Biological Sciences, University of California, San Diego, La Jolla, California , CA, USA.
  • Israelsson E; Bioscience, Translational Science and Experimental Medicine, Research and Early Development, Respiratory & Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Betts J; Bioscience, Translational Science and Experimental Medicine, Research and Early Development, Respiratory & Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Niedzielska M; Bioscience, Research and Early Development, Respiratory & Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Patel SA; Department of Medicine, University of California, San Diego, La Jolla, CA, USA.
  • Duong HG; Department of Medicine, University of California, San Diego, La Jolla, CA, USA.
  • Gerner RR; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA, USA.
  • Hsu CY; Department of Pathology, University of California San Diego, La Jolla, CA, USA.
  • Catley M; Bioscience, Research and Early Development, Respiratory & Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Maciewicz RA; Bioscience, Research and Early Development, Respiratory & Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Chu H; Department of Pathology, University of California San Diego, La Jolla, CA, USA.
  • Raffatellu M; Chiba University-UC San Diego Center for Mucosal Immunology, Allergy, and Vaccines (CU-UCSD cMAV), La Jolla, CA 92093, USA.
  • Chang JT; Center for Microbiome Innovation, University of California, San Diego, La Jolla, CA, USA.
  • Lu LF; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA, USA.
bioRxiv ; 2023 Feb 21.
Article em En | MEDLINE | ID: mdl-36865314
ABSTRACT
Regulatory T (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, here we show that IL-27 is specifically produced by intestinal Treg cells to regulate Th17 immunity. Selectively increased intestinal Th17 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+TCF1+ Treg cell subset that is distinct from previously characterized intestinal Treg cell populations as the main IL-27 producers. Collectively, our study uncovers a novel 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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos