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IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity

Previous mouse and clinical studies demonstrate a link between Th2 intestinal inflammation and induction of the effector phase of food allergy. However, the mechanism by which sensitization and mast cell responses occurs is largely unknown. We demonstrate that interleukin (IL)-9 has an important rol...

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Autores principales: Forbes, Elizabeth E., Groschwitz, Katherine, Abonia, J. Pablo, Brandt, Eric B., Cohen, Elizabeth, Blanchard, Carine, Ahrens, Richard, Seidu, Luqman, McKenzie, Andrew, Strait, Richard, Finkelman, Fred D., Foster, Paul S., Matthaei, Klaus I., Rothenberg, Marc E., Hogan, Simon P.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292227/
https://www.ncbi.nlm.nih.gov/pubmed/18378796
http://dx.doi.org/10.1084/jem.20071046
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author Forbes, Elizabeth E.
Groschwitz, Katherine
Abonia, J. Pablo
Brandt, Eric B.
Cohen, Elizabeth
Blanchard, Carine
Ahrens, Richard
Seidu, Luqman
McKenzie, Andrew
Strait, Richard
Finkelman, Fred D.
Foster, Paul S.
Matthaei, Klaus I.
Rothenberg, Marc E.
Hogan, Simon P.
author_facet Forbes, Elizabeth E.
Groschwitz, Katherine
Abonia, J. Pablo
Brandt, Eric B.
Cohen, Elizabeth
Blanchard, Carine
Ahrens, Richard
Seidu, Luqman
McKenzie, Andrew
Strait, Richard
Finkelman, Fred D.
Foster, Paul S.
Matthaei, Klaus I.
Rothenberg, Marc E.
Hogan, Simon P.
author_sort Forbes, Elizabeth E.
collection PubMed
description Previous mouse and clinical studies demonstrate a link between Th2 intestinal inflammation and induction of the effector phase of food allergy. However, the mechanism by which sensitization and mast cell responses occurs is largely unknown. We demonstrate that interleukin (IL)-9 has an important role in this process. IL-9–deficient mice fail to develop experimental oral antigen–induced intestinal anaphylaxis, and intestinal IL-9 overexpression induces an intestinal anaphylaxis phenotype (intestinal mastocytosis, intestinal permeability, and intravascular leakage). In addition, intestinal IL-9 overexpression predisposes to oral antigen sensitization, which requires mast cells and increased intestinal permeability. These observations demonstrate a central role for IL-9 and mast cells in experimental intestinal permeability in oral antigen sensitization and suggest that IL-9–mediated mast cell responses have an important role in food allergy.
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spelling pubmed-22922272008-10-14 IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity Forbes, Elizabeth E. Groschwitz, Katherine Abonia, J. Pablo Brandt, Eric B. Cohen, Elizabeth Blanchard, Carine Ahrens, Richard Seidu, Luqman McKenzie, Andrew Strait, Richard Finkelman, Fred D. Foster, Paul S. Matthaei, Klaus I. Rothenberg, Marc E. Hogan, Simon P. J Exp Med Articles Previous mouse and clinical studies demonstrate a link between Th2 intestinal inflammation and induction of the effector phase of food allergy. However, the mechanism by which sensitization and mast cell responses occurs is largely unknown. We demonstrate that interleukin (IL)-9 has an important role in this process. IL-9–deficient mice fail to develop experimental oral antigen–induced intestinal anaphylaxis, and intestinal IL-9 overexpression induces an intestinal anaphylaxis phenotype (intestinal mastocytosis, intestinal permeability, and intravascular leakage). In addition, intestinal IL-9 overexpression predisposes to oral antigen sensitization, which requires mast cells and increased intestinal permeability. These observations demonstrate a central role for IL-9 and mast cells in experimental intestinal permeability in oral antigen sensitization and suggest that IL-9–mediated mast cell responses have an important role in food allergy. The Rockefeller University Press 2008-04-14 /pmc/articles/PMC2292227/ /pubmed/18378796 http://dx.doi.org/10.1084/jem.20071046 Text en Copyright © 2008, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Forbes, Elizabeth E.
Groschwitz, Katherine
Abonia, J. Pablo
Brandt, Eric B.
Cohen, Elizabeth
Blanchard, Carine
Ahrens, Richard
Seidu, Luqman
McKenzie, Andrew
Strait, Richard
Finkelman, Fred D.
Foster, Paul S.
Matthaei, Klaus I.
Rothenberg, Marc E.
Hogan, Simon P.
IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
title IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
title_full IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
title_fullStr IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
title_full_unstemmed IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
title_short IL-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
title_sort il-9– and mast cell–mediated intestinal permeability predisposes to oral antigen hypersensitivity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292227/
https://www.ncbi.nlm.nih.gov/pubmed/18378796
http://dx.doi.org/10.1084/jem.20071046
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