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Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells

The gut–liver axis is increasingly considered to play a vital part in the progression of chronic inflammatory gut and liver diseases. Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-dept...

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Autores principales: Atif, Muhammad, Warner, Suz, Oo, Ye H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097019/
https://www.ncbi.nlm.nih.gov/pubmed/30027532
http://dx.doi.org/10.1007/s12072-018-9882-x
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author Atif, Muhammad
Warner, Suz
Oo, Ye H.
author_facet Atif, Muhammad
Warner, Suz
Oo, Ye H.
author_sort Atif, Muhammad
collection PubMed
description The gut–liver axis is increasingly considered to play a vital part in the progression of chronic inflammatory gut and liver diseases. Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-depth the roles of regulatory T cells (Tregs) and mucosal-associated invariant T cells (MAITs) within the context of inflammatory bowel disease, primary sclerosing cholangitis, and non-alcoholic steatohepatitis. Tregs are crucial in maintaining peripheral tolerance and preventing autoimmunity. MAIT cells have a unique ability to rapidly recognize microbial metabolites and mount a local immune response and act as a ‘biliary firewall’ at the gut and biliary epithelial barrier. We also outline how current knowledge can be exploited to develop novel therapies to control the propagation of chronic gut- and liver-related inflammatory and autoimmune conditions. We specifically focus on the nature of the Tregs’ cell therapy product and outline an adjunctive role for low-dose IL-2. All in all, it is clear that translational immunology is at crucial crossroads. The success of ongoing clinical trials in cellular therapies for inflammatory gut and liver conditions could revolutionize the treatment of these conditions and the lives of our patients in the coming years. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12072-018-9882-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60970192018-08-24 Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells Atif, Muhammad Warner, Suz Oo, Ye H. Hepatol Int Review Article The gut–liver axis is increasingly considered to play a vital part in the progression of chronic inflammatory gut and liver diseases. Hence, a detailed understanding of the local and systemic regulatory mechanisms is crucial to develop novel therapeutic approaches. In this review, we discuss in-depth the roles of regulatory T cells (Tregs) and mucosal-associated invariant T cells (MAITs) within the context of inflammatory bowel disease, primary sclerosing cholangitis, and non-alcoholic steatohepatitis. Tregs are crucial in maintaining peripheral tolerance and preventing autoimmunity. MAIT cells have a unique ability to rapidly recognize microbial metabolites and mount a local immune response and act as a ‘biliary firewall’ at the gut and biliary epithelial barrier. We also outline how current knowledge can be exploited to develop novel therapies to control the propagation of chronic gut- and liver-related inflammatory and autoimmune conditions. We specifically focus on the nature of the Tregs’ cell therapy product and outline an adjunctive role for low-dose IL-2. All in all, it is clear that translational immunology is at crucial crossroads. The success of ongoing clinical trials in cellular therapies for inflammatory gut and liver conditions could revolutionize the treatment of these conditions and the lives of our patients in the coming years. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12072-018-9882-x) contains supplementary material, which is available to authorized users. Springer India 2018-07-19 /pmc/articles/PMC6097019/ /pubmed/30027532 http://dx.doi.org/10.1007/s12072-018-9882-x Text en © The Author(s) 2018, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review Article
Atif, Muhammad
Warner, Suz
Oo, Ye H.
Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
title Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
title_full Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
title_fullStr Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
title_full_unstemmed Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
title_short Linking the gut and liver: crosstalk between regulatory T cells and mucosa-associated invariant T cells
title_sort linking the gut and liver: crosstalk between regulatory t cells and mucosa-associated invariant t cells
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097019/
https://www.ncbi.nlm.nih.gov/pubmed/30027532
http://dx.doi.org/10.1007/s12072-018-9882-x
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