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Peyer's Patches: The Immune Sensors of the Intestine

The gut-associated lymphoid tissue (GALT) consists of isolated or aggregated lymphoid follicles forming Peyer's patches (PPs). By their ability to transport luminal antigens and bacteria, PPs can be considered as the immune sensors of the intestine. PPs functions like induction of immune tolera...

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Detalles Bibliográficos
Autores principales: Jung, Camille, Hugot, Jean-Pierre, Barreau, Frédérick
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004000/
https://www.ncbi.nlm.nih.gov/pubmed/21188221
http://dx.doi.org/10.4061/2010/823710
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author Jung, Camille
Hugot, Jean-Pierre
Barreau, Frédérick
author_facet Jung, Camille
Hugot, Jean-Pierre
Barreau, Frédérick
author_sort Jung, Camille
collection PubMed
description The gut-associated lymphoid tissue (GALT) consists of isolated or aggregated lymphoid follicles forming Peyer's patches (PPs). By their ability to transport luminal antigens and bacteria, PPs can be considered as the immune sensors of the intestine. PPs functions like induction of immune tolerance or defense against pathogens result from the complex interplay between immune cells located in the lymphoid follicles and the follicle-associated epithelium. This crosstalk seems to be regulated by pathogen recognition receptors, especially Nod2. Although TLR exerts a limited role in PP homeotasis, Nod2 regulates the number, size, and T-cell composition of PPs, in response to the gut flora. In turn, CD4(+) T-cells present in the PP are able to modulate the paracellular and transcellular permeabilities. Two human disorders, Crohn's disease and graft-versus-host disease are thought to be driven by an abnormal response toward the commensal flora. They have been associated with NOD2 mutations and PP dysfunction.
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spelling pubmed-30040002010-12-23 Peyer's Patches: The Immune Sensors of the Intestine Jung, Camille Hugot, Jean-Pierre Barreau, Frédérick Int J Inflam Review Article The gut-associated lymphoid tissue (GALT) consists of isolated or aggregated lymphoid follicles forming Peyer's patches (PPs). By their ability to transport luminal antigens and bacteria, PPs can be considered as the immune sensors of the intestine. PPs functions like induction of immune tolerance or defense against pathogens result from the complex interplay between immune cells located in the lymphoid follicles and the follicle-associated epithelium. This crosstalk seems to be regulated by pathogen recognition receptors, especially Nod2. Although TLR exerts a limited role in PP homeotasis, Nod2 regulates the number, size, and T-cell composition of PPs, in response to the gut flora. In turn, CD4(+) T-cells present in the PP are able to modulate the paracellular and transcellular permeabilities. Two human disorders, Crohn's disease and graft-versus-host disease are thought to be driven by an abnormal response toward the commensal flora. They have been associated with NOD2 mutations and PP dysfunction. SAGE-Hindawi Access to Research 2010-09-19 /pmc/articles/PMC3004000/ /pubmed/21188221 http://dx.doi.org/10.4061/2010/823710 Text en Copyright © 2010 Camille Jung et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Jung, Camille
Hugot, Jean-Pierre
Barreau, Frédérick
Peyer's Patches: The Immune Sensors of the Intestine
title Peyer's Patches: The Immune Sensors of the Intestine
title_full Peyer's Patches: The Immune Sensors of the Intestine
title_fullStr Peyer's Patches: The Immune Sensors of the Intestine
title_full_unstemmed Peyer's Patches: The Immune Sensors of the Intestine
title_short Peyer's Patches: The Immune Sensors of the Intestine
title_sort peyer's patches: the immune sensors of the intestine
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004000/
https://www.ncbi.nlm.nih.gov/pubmed/21188221
http://dx.doi.org/10.4061/2010/823710
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