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Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts

Crohn’s disease is an inflammatory disease of the gastrointestinal tract characterized by an aberrant response to microbial and environmental triggers. This includes an altered microbiome dominated by Enterobacteriaceae and in particular adherent-invasive E. coli (AIEC). Clinical evidence implicates...

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Autores principales: Shaler, Christopher R., Parco, Alexandra A., Elhenawy, Wael, Dourka, Jasmeen, Jury, Jennifer, Verdu, Elena F., Coombes, Brian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602651/
https://www.ncbi.nlm.nih.gov/pubmed/34795263
http://dx.doi.org/10.1038/s41467-021-26992-4
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author Shaler, Christopher R.
Parco, Alexandra A.
Elhenawy, Wael
Dourka, Jasmeen
Jury, Jennifer
Verdu, Elena F.
Coombes, Brian K.
author_facet Shaler, Christopher R.
Parco, Alexandra A.
Elhenawy, Wael
Dourka, Jasmeen
Jury, Jennifer
Verdu, Elena F.
Coombes, Brian K.
author_sort Shaler, Christopher R.
collection PubMed
description Crohn’s disease is an inflammatory disease of the gastrointestinal tract characterized by an aberrant response to microbial and environmental triggers. This includes an altered microbiome dominated by Enterobacteriaceae and in particular adherent-invasive E. coli (AIEC). Clinical evidence implicates periods of psychological stress in Crohn’s disease exacerbation, and disturbances in the gut microbiome might contribute to the pathogenic mechanism. Here we show that stress-exposed mice develop ileal dysbiosis, dominated by the expansion of Enterobacteriaceae. In an AIEC colonisation model, stress-induced glucocorticoids promote apoptosis of CD45(+)CD90(+) cells that normally produce IL-22, a cytokine that is essential for the maintenance of ileal mucosal barrier integrity. Blockade of glucocorticoid signaling or administration of recombinant IL-22 restores mucosal immunity, prevents ileal dysbiosis, and blocks AIEC expansion. We conclude that psychological stress impairs IL-22-driven protective immunity in the gut, which creates a favorable niche for the expansion of pathobionts that have been implicated in Crohn’s disease. Importantly, this work also shows that immunomodulation can counteract the negative effects of psychological stress on gut immunity and hence disease-associated dysbiosis.
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spelling pubmed-86026512021-12-03 Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts Shaler, Christopher R. Parco, Alexandra A. Elhenawy, Wael Dourka, Jasmeen Jury, Jennifer Verdu, Elena F. Coombes, Brian K. Nat Commun Article Crohn’s disease is an inflammatory disease of the gastrointestinal tract characterized by an aberrant response to microbial and environmental triggers. This includes an altered microbiome dominated by Enterobacteriaceae and in particular adherent-invasive E. coli (AIEC). Clinical evidence implicates periods of psychological stress in Crohn’s disease exacerbation, and disturbances in the gut microbiome might contribute to the pathogenic mechanism. Here we show that stress-exposed mice develop ileal dysbiosis, dominated by the expansion of Enterobacteriaceae. In an AIEC colonisation model, stress-induced glucocorticoids promote apoptosis of CD45(+)CD90(+) cells that normally produce IL-22, a cytokine that is essential for the maintenance of ileal mucosal barrier integrity. Blockade of glucocorticoid signaling or administration of recombinant IL-22 restores mucosal immunity, prevents ileal dysbiosis, and blocks AIEC expansion. We conclude that psychological stress impairs IL-22-driven protective immunity in the gut, which creates a favorable niche for the expansion of pathobionts that have been implicated in Crohn’s disease. Importantly, this work also shows that immunomodulation can counteract the negative effects of psychological stress on gut immunity and hence disease-associated dysbiosis. Nature Publishing Group UK 2021-11-18 /pmc/articles/PMC8602651/ /pubmed/34795263 http://dx.doi.org/10.1038/s41467-021-26992-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shaler, Christopher R.
Parco, Alexandra A.
Elhenawy, Wael
Dourka, Jasmeen
Jury, Jennifer
Verdu, Elena F.
Coombes, Brian K.
Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts
title Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts
title_full Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts
title_fullStr Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts
title_full_unstemmed Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts
title_short Psychological stress impairs IL22-driven protective gut mucosal immunity against colonising pathobionts
title_sort psychological stress impairs il22-driven protective gut mucosal immunity against colonising pathobionts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602651/
https://www.ncbi.nlm.nih.gov/pubmed/34795263
http://dx.doi.org/10.1038/s41467-021-26992-4
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