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Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food
The increasing prevalence of food allergies has been linked to reduced commensal microbial diversity. In this article, we describe two features of allergy-protective Clostridia that contribute to their beneficial effects. Some Clostridial taxa bear flagella (a ligand for TLR5) and produce indole (a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10697505/ https://www.ncbi.nlm.nih.gov/pubmed/37742185 http://dx.doi.org/10.1016/j.celrep.2023.113153 |
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author | Kemter, Andrea M. Patry, Robert T. Arnold, Jack Hesser, Lauren A. Campbell, Evelyn Ionescu, Edward Mimee, Mark Wang, Shan Nagler, Cathryn R. |
author_facet | Kemter, Andrea M. Patry, Robert T. Arnold, Jack Hesser, Lauren A. Campbell, Evelyn Ionescu, Edward Mimee, Mark Wang, Shan Nagler, Cathryn R. |
author_sort | Kemter, Andrea M. |
collection | PubMed |
description | The increasing prevalence of food allergies has been linked to reduced commensal microbial diversity. In this article, we describe two features of allergy-protective Clostridia that contribute to their beneficial effects. Some Clostridial taxa bear flagella (a ligand for TLR5) and produce indole (a ligand for the aryl hydrocarbon receptor [AhR]). Lysates and flagella from a Clostridia consortium induced interleukin-22 (IL-22) secretion from ileal explants. IL-22 production is abrogated in explants from mice in which TLR5 or MyD88 signaling is deficient either globally or conditionally in CD11c(+) antigen-presenting cells. AhR signaling in RORγt(+) cells is necessary for the induction of IL-22. Mice deficient in AhR in RORγt(+) cells exhibit increased intestinal permeability and are more susceptible to an anaphylactic response to food. Our findings implicate TLR5 and AhR signaling in a molecular mechanism by which commensal Clostridia protect against allergic responses to food. |
format | Online Article Text |
id | pubmed-10697505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-106975052023-12-05 Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food Kemter, Andrea M. Patry, Robert T. Arnold, Jack Hesser, Lauren A. Campbell, Evelyn Ionescu, Edward Mimee, Mark Wang, Shan Nagler, Cathryn R. Cell Rep Article The increasing prevalence of food allergies has been linked to reduced commensal microbial diversity. In this article, we describe two features of allergy-protective Clostridia that contribute to their beneficial effects. Some Clostridial taxa bear flagella (a ligand for TLR5) and produce indole (a ligand for the aryl hydrocarbon receptor [AhR]). Lysates and flagella from a Clostridia consortium induced interleukin-22 (IL-22) secretion from ileal explants. IL-22 production is abrogated in explants from mice in which TLR5 or MyD88 signaling is deficient either globally or conditionally in CD11c(+) antigen-presenting cells. AhR signaling in RORγt(+) cells is necessary for the induction of IL-22. Mice deficient in AhR in RORγt(+) cells exhibit increased intestinal permeability and are more susceptible to an anaphylactic response to food. Our findings implicate TLR5 and AhR signaling in a molecular mechanism by which commensal Clostridia protect against allergic responses to food. 2023-10-31 2023-09-25 /pmc/articles/PMC10697505/ /pubmed/37742185 http://dx.doi.org/10.1016/j.celrep.2023.113153 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Kemter, Andrea M. Patry, Robert T. Arnold, Jack Hesser, Lauren A. Campbell, Evelyn Ionescu, Edward Mimee, Mark Wang, Shan Nagler, Cathryn R. Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food |
title | Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food |
title_full | Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food |
title_fullStr | Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food |
title_full_unstemmed | Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food |
title_short | Commensal bacteria signal through TLR5 and AhR to improve barrier integrity and prevent allergic responses to food |
title_sort | commensal bacteria signal through tlr5 and ahr to improve barrier integrity and prevent allergic responses to food |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10697505/ https://www.ncbi.nlm.nih.gov/pubmed/37742185 http://dx.doi.org/10.1016/j.celrep.2023.113153 |
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