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Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity

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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980002/
https://www.ncbi.nlm.nih.gov/pubmed/36865314
http://dx.doi.org/10.1101/2023.02.20.529261
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author 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
author_facet 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
author_sort Lin, Chia-Hao
collection PubMed
description 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.
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spelling pubmed-99800022023-03-03 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 bioRxiv Article 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. Cold Spring Harbor Laboratory 2023-02-21 /pmc/articles/PMC9980002/ /pubmed/36865314 http://dx.doi.org/10.1101/2023.02.20.529261 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
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
Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity
title Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity
title_full Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity
title_fullStr Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity
title_full_unstemmed Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity
title_short Selective IL-27 production by intestinal regulatory T cells permits gut-specific regulation of Th17 immunity
title_sort selective il-27 production by intestinal regulatory t cells permits gut-specific regulation of th17 immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980002/
https://www.ncbi.nlm.nih.gov/pubmed/36865314
http://dx.doi.org/10.1101/2023.02.20.529261
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