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The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma

Allergic asthma is a chronic airway disorder characterized by airway inflammation, mucus hypersecretion, and airway hyperresponsiveness (AHR). A murine model of asthma was used to examine the antiasthmatic effect of inhaled inactived Mycobacterium phlei (M. phlei). AHR, neutrophil levels, eosinophil...

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Autores principales: Ming, Moyu, Li, Chaoqian, Luo, Zhixi, Lv, Shengqiu, Sun, Qixiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364862/
https://www.ncbi.nlm.nih.gov/pubmed/28035388
http://dx.doi.org/10.3892/mmr.2016.6087
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author Ming, Moyu
Li, Chaoqian
Luo, Zhixi
Lv, Shengqiu
Sun, Qixiang
author_facet Ming, Moyu
Li, Chaoqian
Luo, Zhixi
Lv, Shengqiu
Sun, Qixiang
author_sort Ming, Moyu
collection PubMed
description Allergic asthma is a chronic airway disorder characterized by airway inflammation, mucus hypersecretion, and airway hyperresponsiveness (AHR). A murine model of asthma was used to examine the antiasthmatic effect of inhaled inactived Mycobacterium phlei (M. phlei). AHR, neutrophil levels, eosinophil levels and levels of interleukin (IL)-17 and IL-23 receptor (IL-23R) were monitored. The results demonstrated that inactivated M. phlei alleviates the IL-17+γδT cell-mediated immune response and attenuates airway inflammation and airway hyperresponsiveness in the asthmatic murine lung, partially through inhibiting the expression of IL-23R. In conclusion, inactivated M. phlei may be an effective antiasthmatic treatment, regulating IL-17-producing γδT (IL-17+γδT) cell-mediated airway inflammation and airway hyperresponsiveness to relieve the symptoms of mice with asthma.
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spelling pubmed-53648622017-05-15 The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma Ming, Moyu Li, Chaoqian Luo, Zhixi Lv, Shengqiu Sun, Qixiang Mol Med Rep Articles Allergic asthma is a chronic airway disorder characterized by airway inflammation, mucus hypersecretion, and airway hyperresponsiveness (AHR). A murine model of asthma was used to examine the antiasthmatic effect of inhaled inactived Mycobacterium phlei (M. phlei). AHR, neutrophil levels, eosinophil levels and levels of interleukin (IL)-17 and IL-23 receptor (IL-23R) were monitored. The results demonstrated that inactivated M. phlei alleviates the IL-17+γδT cell-mediated immune response and attenuates airway inflammation and airway hyperresponsiveness in the asthmatic murine lung, partially through inhibiting the expression of IL-23R. In conclusion, inactivated M. phlei may be an effective antiasthmatic treatment, regulating IL-17-producing γδT (IL-17+γδT) cell-mediated airway inflammation and airway hyperresponsiveness to relieve the symptoms of mice with asthma. D.A. Spandidos 2017-02 2016-12-29 /pmc/articles/PMC5364862/ /pubmed/28035388 http://dx.doi.org/10.3892/mmr.2016.6087 Text en Copyright: © Ming et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Ming, Moyu
Li, Chaoqian
Luo, Zhixi
Lv, Shengqiu
Sun, Qixiang
The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma
title The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma
title_full The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma
title_fullStr The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma
title_full_unstemmed The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma
title_short The effect of inhaled inactived Mycobacterium phlei as a treatment for asthma
title_sort effect of inhaled inactived mycobacterium phlei as a treatment for asthma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364862/
https://www.ncbi.nlm.nih.gov/pubmed/28035388
http://dx.doi.org/10.3892/mmr.2016.6087
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