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A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease
There is an unmet need for effective new and innovative treatments for asthma. It is becoming increasingly evident that bacterial stimulation can have beneficial effects at attenuating allergic airway disease through immune modulation. Our aim was to test the ability of a novel inactivated microbe-d...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062168/ https://www.ncbi.nlm.nih.gov/pubmed/27734946 http://dx.doi.org/10.1038/srep35338 |
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author | Bazett, Mark Biala, Agnieszka Huff, Ryan D. Bosiljcic, Momir Gunn, Hal Kalyan, Shirin Hirota, Jeremy A. |
author_facet | Bazett, Mark Biala, Agnieszka Huff, Ryan D. Bosiljcic, Momir Gunn, Hal Kalyan, Shirin Hirota, Jeremy A. |
author_sort | Bazett, Mark |
collection | PubMed |
description | There is an unmet need for effective new and innovative treatments for asthma. It is becoming increasingly evident that bacterial stimulation can have beneficial effects at attenuating allergic airway disease through immune modulation. Our aim was to test the ability of a novel inactivated microbe-derived therapeutic based on Klebsiella (KB) in a model of allergic airway disease in mice. BALB/c mice were exposed intranasally to house dust mite (HDM) for two weeks. Mice were treated prophylactically via subcutaneous route with either KB or placebo for one week prior to HDM exposure and throughout the two week exposure period. 24 hours after the last exposure, lungs were analysed for inflammatory cell infiltrate, gene expression, cytokine levels, goblet cell metaplasia, and serum was analysed for allergen-specific serum IgE levels. HDM exposed mice developed goblet cell hyperplasia, elevated allergen-specific serum IgE, airway eosinophilia, and a concomitant increase in T(H)2 cytokines including IL-4, IL-13 and IL-5. Treatment with KB attenuated HDM-mediated airway eosinophilia, total bronchoalveolar lavage (BAL) cell numbers, BAL T(H)2 cytokine production, and goblet cell metaplasia. Our prophylactic intervention study illustrates the potential of subcutaneous treatment with bacterial derived biologics as a promising approach for allergic airway disease treatment. |
format | Online Article Text |
id | pubmed-5062168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50621682016-10-24 A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease Bazett, Mark Biala, Agnieszka Huff, Ryan D. Bosiljcic, Momir Gunn, Hal Kalyan, Shirin Hirota, Jeremy A. Sci Rep Article There is an unmet need for effective new and innovative treatments for asthma. It is becoming increasingly evident that bacterial stimulation can have beneficial effects at attenuating allergic airway disease through immune modulation. Our aim was to test the ability of a novel inactivated microbe-derived therapeutic based on Klebsiella (KB) in a model of allergic airway disease in mice. BALB/c mice were exposed intranasally to house dust mite (HDM) for two weeks. Mice were treated prophylactically via subcutaneous route with either KB or placebo for one week prior to HDM exposure and throughout the two week exposure period. 24 hours after the last exposure, lungs were analysed for inflammatory cell infiltrate, gene expression, cytokine levels, goblet cell metaplasia, and serum was analysed for allergen-specific serum IgE levels. HDM exposed mice developed goblet cell hyperplasia, elevated allergen-specific serum IgE, airway eosinophilia, and a concomitant increase in T(H)2 cytokines including IL-4, IL-13 and IL-5. Treatment with KB attenuated HDM-mediated airway eosinophilia, total bronchoalveolar lavage (BAL) cell numbers, BAL T(H)2 cytokine production, and goblet cell metaplasia. Our prophylactic intervention study illustrates the potential of subcutaneous treatment with bacterial derived biologics as a promising approach for allergic airway disease treatment. Nature Publishing Group 2016-10-13 /pmc/articles/PMC5062168/ /pubmed/27734946 http://dx.doi.org/10.1038/srep35338 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bazett, Mark Biala, Agnieszka Huff, Ryan D. Bosiljcic, Momir Gunn, Hal Kalyan, Shirin Hirota, Jeremy A. A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
title | A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
title_full | A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
title_fullStr | A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
title_full_unstemmed | A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
title_short | A novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
title_sort | novel microbe-based treatment that attenuates the inflammatory profile in a mouse model of allergic airway disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062168/ https://www.ncbi.nlm.nih.gov/pubmed/27734946 http://dx.doi.org/10.1038/srep35338 |
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