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Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo

Eosinophils natively inhabit the small intestine, but a functional role for them there has remained elusive. Here, we show that eosinophil-deficient mice were protected from induction of Th2-mediated peanut food allergy and anaphylaxis, and Th2 priming was restored by reconstitution with il4(+/+) or...

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Autores principales: Chu, Derek K., Jimenez-Saiz, Rodrigo, Verschoor, Christopher P., Walker, Tina D., Goncharova, Susanna, Llop-Guevara, Alba, Shen, Pamela, Gordon, Melissa E., Barra, Nicole G., Bassett, Jennifer D., Kong, Joshua, Fattouh, Ramzi, McCoy, Kathy D., Bowdish, Dawn M., Erjefält, Jonas S., Pabst, Oliver, Humbles, Alison A., Kolbeck, Roland, Waserman, Susan, Jordana, Manel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113937/
https://www.ncbi.nlm.nih.gov/pubmed/25071163
http://dx.doi.org/10.1084/jem.20131800
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author Chu, Derek K.
Jimenez-Saiz, Rodrigo
Verschoor, Christopher P.
Walker, Tina D.
Goncharova, Susanna
Llop-Guevara, Alba
Shen, Pamela
Gordon, Melissa E.
Barra, Nicole G.
Bassett, Jennifer D.
Kong, Joshua
Fattouh, Ramzi
McCoy, Kathy D.
Bowdish, Dawn M.
Erjefält, Jonas S.
Pabst, Oliver
Humbles, Alison A.
Kolbeck, Roland
Waserman, Susan
Jordana, Manel
author_facet Chu, Derek K.
Jimenez-Saiz, Rodrigo
Verschoor, Christopher P.
Walker, Tina D.
Goncharova, Susanna
Llop-Guevara, Alba
Shen, Pamela
Gordon, Melissa E.
Barra, Nicole G.
Bassett, Jennifer D.
Kong, Joshua
Fattouh, Ramzi
McCoy, Kathy D.
Bowdish, Dawn M.
Erjefält, Jonas S.
Pabst, Oliver
Humbles, Alison A.
Kolbeck, Roland
Waserman, Susan
Jordana, Manel
author_sort Chu, Derek K.
collection PubMed
description Eosinophils natively inhabit the small intestine, but a functional role for them there has remained elusive. Here, we show that eosinophil-deficient mice were protected from induction of Th2-mediated peanut food allergy and anaphylaxis, and Th2 priming was restored by reconstitution with il4(+/+) or il4(−/−) eosinophils. Eosinophils controlled CD103(+) dendritic cell (DC) activation and migration from the intestine to draining lymph nodes, events necessary for Th2 priming. Eosinophil activation in vitro and in vivo led to degranulation of eosinophil peroxidase, a granule protein whose enzymatic activity promoted DC activation in mice and humans in vitro, and intestinal and extraintestinal mouse DC activation and mobilization to lymph nodes in vivo. Further, eosinophil peroxidase enhanced responses to ovalbumin seen after immunization. Thus, eosinophils can be critical contributors to the intestinal immune system, and granule-mediated shaping of DC responses can promote both intestinal and extraintestinal adaptive immunity.
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spelling pubmed-41139372015-01-28 Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo Chu, Derek K. Jimenez-Saiz, Rodrigo Verschoor, Christopher P. Walker, Tina D. Goncharova, Susanna Llop-Guevara, Alba Shen, Pamela Gordon, Melissa E. Barra, Nicole G. Bassett, Jennifer D. Kong, Joshua Fattouh, Ramzi McCoy, Kathy D. Bowdish, Dawn M. Erjefält, Jonas S. Pabst, Oliver Humbles, Alison A. Kolbeck, Roland Waserman, Susan Jordana, Manel J Exp Med Article Eosinophils natively inhabit the small intestine, but a functional role for them there has remained elusive. Here, we show that eosinophil-deficient mice were protected from induction of Th2-mediated peanut food allergy and anaphylaxis, and Th2 priming was restored by reconstitution with il4(+/+) or il4(−/−) eosinophils. Eosinophils controlled CD103(+) dendritic cell (DC) activation and migration from the intestine to draining lymph nodes, events necessary for Th2 priming. Eosinophil activation in vitro and in vivo led to degranulation of eosinophil peroxidase, a granule protein whose enzymatic activity promoted DC activation in mice and humans in vitro, and intestinal and extraintestinal mouse DC activation and mobilization to lymph nodes in vivo. Further, eosinophil peroxidase enhanced responses to ovalbumin seen after immunization. Thus, eosinophils can be critical contributors to the intestinal immune system, and granule-mediated shaping of DC responses can promote both intestinal and extraintestinal adaptive immunity. The Rockefeller University Press 2014-07-28 /pmc/articles/PMC4113937/ /pubmed/25071163 http://dx.doi.org/10.1084/jem.20131800 Text en © 2014 Chu et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Article
Chu, Derek K.
Jimenez-Saiz, Rodrigo
Verschoor, Christopher P.
Walker, Tina D.
Goncharova, Susanna
Llop-Guevara, Alba
Shen, Pamela
Gordon, Melissa E.
Barra, Nicole G.
Bassett, Jennifer D.
Kong, Joshua
Fattouh, Ramzi
McCoy, Kathy D.
Bowdish, Dawn M.
Erjefält, Jonas S.
Pabst, Oliver
Humbles, Alison A.
Kolbeck, Roland
Waserman, Susan
Jordana, Manel
Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo
title Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo
title_full Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo
title_fullStr Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo
title_full_unstemmed Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo
title_short Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo
title_sort indigenous enteric eosinophils control dcs to initiate a primary th2 immune response in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113937/
https://www.ncbi.nlm.nih.gov/pubmed/25071163
http://dx.doi.org/10.1084/jem.20131800
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