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

Christopher R. Shaler, Alexandra A. Parco, Wael Elhenawy, Jasmeen Dourka, Jennifer Jury, Elena F. Verdu and Brian K. Coombes ()
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Christopher R. Shaler: McMaster University
Alexandra A. Parco: McMaster University
Wael Elhenawy: McMaster University
Jasmeen Dourka: McMaster University
Jennifer Jury: Farncombe Family Digestive Health Research Institute
Elena F. Verdu: Farncombe Family Digestive Health Research Institute
Brian K. Coombes: McMaster University

Nature Communications, 2021, vol. 12, issue 1, 1-17

Abstract: Abstract 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.

Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26992-4

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DOI: 10.1038/s41467-021-26992-4

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