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Cocoa Diet and Antibody Immune Response in Preclinical Studies

The ability of cocoa to interact with the immune system in vitro and in vivo has been described. In the latter context, a cocoa-enriched diet in healthy rats was able to modify the immune system’s functionality. This fact could be observed in the composition and functionality of lymphoid tissues, su...

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Autores principales: Camps-Bossacoma, Mariona, Massot-Cladera, Malen, Abril-Gil, Mar, Franch, Angels, Pérez-Cano, Francisco J., Castell, Margarida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484773/
https://www.ncbi.nlm.nih.gov/pubmed/28702458
http://dx.doi.org/10.3389/fnut.2017.00028
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author Camps-Bossacoma, Mariona
Massot-Cladera, Malen
Abril-Gil, Mar
Franch, Angels
Pérez-Cano, Francisco J.
Castell, Margarida
author_facet Camps-Bossacoma, Mariona
Massot-Cladera, Malen
Abril-Gil, Mar
Franch, Angels
Pérez-Cano, Francisco J.
Castell, Margarida
author_sort Camps-Bossacoma, Mariona
collection PubMed
description The ability of cocoa to interact with the immune system in vitro and in vivo has been described. In the latter context, a cocoa-enriched diet in healthy rats was able to modify the immune system’s functionality. This fact could be observed in the composition and functionality of lymphoid tissues, such as the thymus, spleen, and lymph nodes. Consequently, immune effector mechanisms, such as antibody synthesis, were modified. A cocoa-enriched diet in young rats was able to attenuate the serum levels of immunoglobulin (Ig) G, IgM, and IgA and also the intestinal IgM and IgA secretion. Moreover, in immunized rats, the intake of cocoa decreased specific IgG1, IgG2a, IgG2c, and IgM concentrations in serum. This immune-regulator potential was then tested in disease models in which antibodies play a pathogenic role. A cocoa-enriched diet was able to partially prevent the synthesis of autoantibodies in a model of autoimmune arthritis in rats and was also able to protect against IgE and T helper 2-related antibody synthesis in two rat models of allergy. Likewise, a cocoa-enriched diet prevented an oral sensitization process in young rats. In this review, we will focus on the influence of cocoa on the acquired branch of the immune function. Therefore, we will focus on how a cocoa diet influences lymphocyte function both in the systemic and intestinal immune system. Likewise, its potential role in preventing some antibody-induced immune diseases is also included. Although further studies must characterize the particular cocoa components responsible for such effects and nutritional studies in humans need to be carried out, cocoa has potential as a nutraceutical agent in some hypersensitivity status.
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spelling pubmed-54847732017-07-12 Cocoa Diet and Antibody Immune Response in Preclinical Studies Camps-Bossacoma, Mariona Massot-Cladera, Malen Abril-Gil, Mar Franch, Angels Pérez-Cano, Francisco J. Castell, Margarida Front Nutr Nutrition The ability of cocoa to interact with the immune system in vitro and in vivo has been described. In the latter context, a cocoa-enriched diet in healthy rats was able to modify the immune system’s functionality. This fact could be observed in the composition and functionality of lymphoid tissues, such as the thymus, spleen, and lymph nodes. Consequently, immune effector mechanisms, such as antibody synthesis, were modified. A cocoa-enriched diet in young rats was able to attenuate the serum levels of immunoglobulin (Ig) G, IgM, and IgA and also the intestinal IgM and IgA secretion. Moreover, in immunized rats, the intake of cocoa decreased specific IgG1, IgG2a, IgG2c, and IgM concentrations in serum. This immune-regulator potential was then tested in disease models in which antibodies play a pathogenic role. A cocoa-enriched diet was able to partially prevent the synthesis of autoantibodies in a model of autoimmune arthritis in rats and was also able to protect against IgE and T helper 2-related antibody synthesis in two rat models of allergy. Likewise, a cocoa-enriched diet prevented an oral sensitization process in young rats. In this review, we will focus on the influence of cocoa on the acquired branch of the immune function. Therefore, we will focus on how a cocoa diet influences lymphocyte function both in the systemic and intestinal immune system. Likewise, its potential role in preventing some antibody-induced immune diseases is also included. Although further studies must characterize the particular cocoa components responsible for such effects and nutritional studies in humans need to be carried out, cocoa has potential as a nutraceutical agent in some hypersensitivity status. Frontiers Media S.A. 2017-06-27 /pmc/articles/PMC5484773/ /pubmed/28702458 http://dx.doi.org/10.3389/fnut.2017.00028 Text en Copyright © 2017 Camps-Bossacoma, Massot-Cladera, Abril-Gil, Franch, Pérez-Cano and Castell. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Camps-Bossacoma, Mariona
Massot-Cladera, Malen
Abril-Gil, Mar
Franch, Angels
Pérez-Cano, Francisco J.
Castell, Margarida
Cocoa Diet and Antibody Immune Response in Preclinical Studies
title Cocoa Diet and Antibody Immune Response in Preclinical Studies
title_full Cocoa Diet and Antibody Immune Response in Preclinical Studies
title_fullStr Cocoa Diet and Antibody Immune Response in Preclinical Studies
title_full_unstemmed Cocoa Diet and Antibody Immune Response in Preclinical Studies
title_short Cocoa Diet and Antibody Immune Response in Preclinical Studies
title_sort cocoa diet and antibody immune response in preclinical studies
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484773/
https://www.ncbi.nlm.nih.gov/pubmed/28702458
http://dx.doi.org/10.3389/fnut.2017.00028
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