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Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity
β-Glucan is a polysaccharide that can be extracted from fungal cell walls. Wellmune WGP(®), a preparation of β-1,3/1,6-glucans, is a dietary supplement that has immunomodulating properties. Here we investigated the effect WGP had on a mouse model of asthma. OVA-induced asthma in mice is characterize...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916077/ https://www.ncbi.nlm.nih.gov/pubmed/27390655 http://dx.doi.org/10.1186/s40064-016-2501-1 |
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author | Burg, Ashley R. Quigley, Laura Jones, Adam V. O’Connor, Geraldine M. Boelte, Kimberly McVicar, Daniel W. Orr, Selinda J. |
author_facet | Burg, Ashley R. Quigley, Laura Jones, Adam V. O’Connor, Geraldine M. Boelte, Kimberly McVicar, Daniel W. Orr, Selinda J. |
author_sort | Burg, Ashley R. |
collection | PubMed |
description | β-Glucan is a polysaccharide that can be extracted from fungal cell walls. Wellmune WGP(®), a preparation of β-1,3/1,6-glucans, is a dietary supplement that has immunomodulating properties. Here we investigated the effect WGP had on a mouse model of asthma. OVA-induced asthma in mice is characterized by infiltration of eosinophils into the lung, production of Th2 cytokines and IgE. Daily oral administration of WGP (400 µg) significantly reduced the influx of eosinophils into the lungs of OVA-challenged mice compared to control mice. In addition, WGP inhibited pulmonary production of Th2 cytokines (IL-4, IL-5, IL-13), however serum IgE levels were unaffected by WGP treatment. These data indicate that WGP could potentially be useful as an oral supplement for some asthma patients, however, it would need to be combined with therapies that target other aspects of the disease such as IgE levels. As such, further studies that examine the potential of WGP in combination with other therapies should be explored. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-016-2501-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4916077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49160772016-07-07 Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity Burg, Ashley R. Quigley, Laura Jones, Adam V. O’Connor, Geraldine M. Boelte, Kimberly McVicar, Daniel W. Orr, Selinda J. Springerplus Research β-Glucan is a polysaccharide that can be extracted from fungal cell walls. Wellmune WGP(®), a preparation of β-1,3/1,6-glucans, is a dietary supplement that has immunomodulating properties. Here we investigated the effect WGP had on a mouse model of asthma. OVA-induced asthma in mice is characterized by infiltration of eosinophils into the lung, production of Th2 cytokines and IgE. Daily oral administration of WGP (400 µg) significantly reduced the influx of eosinophils into the lungs of OVA-challenged mice compared to control mice. In addition, WGP inhibited pulmonary production of Th2 cytokines (IL-4, IL-5, IL-13), however serum IgE levels were unaffected by WGP treatment. These data indicate that WGP could potentially be useful as an oral supplement for some asthma patients, however, it would need to be combined with therapies that target other aspects of the disease such as IgE levels. As such, further studies that examine the potential of WGP in combination with other therapies should be explored. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-016-2501-1) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-06-21 /pmc/articles/PMC4916077/ /pubmed/27390655 http://dx.doi.org/10.1186/s40064-016-2501-1 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Burg, Ashley R. Quigley, Laura Jones, Adam V. O’Connor, Geraldine M. Boelte, Kimberly McVicar, Daniel W. Orr, Selinda J. Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity |
title | Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity |
title_full | Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity |
title_fullStr | Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity |
title_full_unstemmed | Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity |
title_short | Orally administered β-glucan attenuates the Th2 response in a model of airway hypersensitivity |
title_sort | orally administered β-glucan attenuates the th2 response in a model of airway hypersensitivity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916077/ https://www.ncbi.nlm.nih.gov/pubmed/27390655 http://dx.doi.org/10.1186/s40064-016-2501-1 |
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