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CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis

Monoclonal antibodies (mAb) have been shown effective in inducing immune tolerance in a range of animal models of autoimmunity, allergy, and transplantation. We investigated whether CD4-blockade, effective in inducing transplantation tolerance, could prevent systemic immune responses leading to anap...

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Detalles Bibliográficos
Autores principales: Duarte, Joana, Caridade, Marta, Graca, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341953/
https://www.ncbi.nlm.nih.gov/pubmed/22566846
http://dx.doi.org/10.3389/fimmu.2011.00056
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author Duarte, Joana
Caridade, Marta
Graca, Luis
author_facet Duarte, Joana
Caridade, Marta
Graca, Luis
author_sort Duarte, Joana
collection PubMed
description Monoclonal antibodies (mAb) have been shown effective in inducing immune tolerance in a range of animal models of autoimmunity, allergy, and transplantation. We investigated whether CD4-blockade, effective in inducing transplantation tolerance, could prevent systemic immune responses leading to anaphylaxis. We found that treatment with a non-depleting anti-CD4 mAb could prevent peanut-induced anaphylaxis following subsequent systemic exposure to crude peanut extract (CPE). Furthermore, the effect of CD4-blockade did not interfere with overall immune competence, as anti-CD4 treated mice remained fully competent to respond to unrelated antigens. Protection from anaphylaxis correlated with increased frequency of Foxp3(+) regulatory T cells (Treg), and was abrogated following Treg depletion. Taken together our data suggest that activation of T cells by CPE in presence of CD4-blockade leads to Treg expansion that can prevent peanut-induced anaphylaxis.
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spelling pubmed-33419532012-05-07 CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis Duarte, Joana Caridade, Marta Graca, Luis Front Immunol Immunology Monoclonal antibodies (mAb) have been shown effective in inducing immune tolerance in a range of animal models of autoimmunity, allergy, and transplantation. We investigated whether CD4-blockade, effective in inducing transplantation tolerance, could prevent systemic immune responses leading to anaphylaxis. We found that treatment with a non-depleting anti-CD4 mAb could prevent peanut-induced anaphylaxis following subsequent systemic exposure to crude peanut extract (CPE). Furthermore, the effect of CD4-blockade did not interfere with overall immune competence, as anti-CD4 treated mice remained fully competent to respond to unrelated antigens. Protection from anaphylaxis correlated with increased frequency of Foxp3(+) regulatory T cells (Treg), and was abrogated following Treg depletion. Taken together our data suggest that activation of T cells by CPE in presence of CD4-blockade leads to Treg expansion that can prevent peanut-induced anaphylaxis. Frontiers Research Foundation 2011-10-19 /pmc/articles/PMC3341953/ /pubmed/22566846 http://dx.doi.org/10.3389/fimmu.2011.00056 Text en Copyright © 2011 Duarte, Caridade and Graca. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Immunology
Duarte, Joana
Caridade, Marta
Graca, Luis
CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis
title CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis
title_full CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis
title_fullStr CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis
title_full_unstemmed CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis
title_short CD4-Blockade Can Induce Protection from Peanut-Induced Anaphylaxis
title_sort cd4-blockade can induce protection from peanut-induced anaphylaxis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341953/
https://www.ncbi.nlm.nih.gov/pubmed/22566846
http://dx.doi.org/10.3389/fimmu.2011.00056
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