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Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells

PURPOSE: Bacillus Calmette-Guérin (BCG) is known to suppress the asthmatic responses in a murine model of asthma and to induce dendritic cells (DCs) maturation. Mature DCs play a crucial role in the differentiation of regulatory T cells (Tregs), which are known to regulate allergic inflammatory resp...

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Autores principales: Kim, Young-Joon, Kim, Ha-Jung, Kang, Mi-Jin, Yu, Ho-Sung, Seo, Ju-Hee, Kim, Hyung-Young, Park, Seoung-Ju, Lee, Yong-Chul, Hong, Soo-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021237/
https://www.ncbi.nlm.nih.gov/pubmed/24843794
http://dx.doi.org/10.4168/aair.2014.6.3.201
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author Kim, Young-Joon
Kim, Ha-Jung
Kang, Mi-Jin
Yu, Ho-Sung
Seo, Ju-Hee
Kim, Hyung-Young
Park, Seoung-Ju
Lee, Yong-Chul
Hong, Soo-Jong
author_facet Kim, Young-Joon
Kim, Ha-Jung
Kang, Mi-Jin
Yu, Ho-Sung
Seo, Ju-Hee
Kim, Hyung-Young
Park, Seoung-Ju
Lee, Yong-Chul
Hong, Soo-Jong
author_sort Kim, Young-Joon
collection PubMed
description PURPOSE: Bacillus Calmette-Guérin (BCG) is known to suppress the asthmatic responses in a murine model of asthma and to induce dendritic cells (DCs) maturation. Mature DCs play a crucial role in the differentiation of regulatory T cells (Tregs), which are known to regulate allergic inflammatory responses. To investigate whether BCG regulates Tregs in a DCs-mediated manner, we analyzed in a murine model of asthma. METHODS: BALB/c mice were injected intraperitoneally with BCG or intravenously with BCG-stimulated DCs and then sensitized and challenged with ovalbumin (OVA). Mice were analysed for bronchial hyperresponsiveness (BHR), the influx of inflammatory cells in the bronchoalveolar lavage (BAL) fluid, and histopathological changes in the lung. To identify the mechanisms, IgE, IgG(1) and IgG(2a) in the serum were analysed and the CD25(+) Tregs in the mice were depleted with anti-CD25 monoclonal antibody (mAb). RESULTS: BCG and the transfer of BCG-stimulated DCs both suppressed all aspects of the asthmatic responses, namely, BHR, the production of total IgE and OVA-specific IgE and IgGs, and pulmonary eosinophilic inflammation. Anti-CD25mAb treatment reversed these effects. CONCLUSIONS: BCG can attenuate the allergic inflammation in a mouse model of asthma by a Tregs-related mechanism that is mediated by DCs.
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spelling pubmed-40212372014-05-19 Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells Kim, Young-Joon Kim, Ha-Jung Kang, Mi-Jin Yu, Ho-Sung Seo, Ju-Hee Kim, Hyung-Young Park, Seoung-Ju Lee, Yong-Chul Hong, Soo-Jong Allergy Asthma Immunol Res Original Article PURPOSE: Bacillus Calmette-Guérin (BCG) is known to suppress the asthmatic responses in a murine model of asthma and to induce dendritic cells (DCs) maturation. Mature DCs play a crucial role in the differentiation of regulatory T cells (Tregs), which are known to regulate allergic inflammatory responses. To investigate whether BCG regulates Tregs in a DCs-mediated manner, we analyzed in a murine model of asthma. METHODS: BALB/c mice were injected intraperitoneally with BCG or intravenously with BCG-stimulated DCs and then sensitized and challenged with ovalbumin (OVA). Mice were analysed for bronchial hyperresponsiveness (BHR), the influx of inflammatory cells in the bronchoalveolar lavage (BAL) fluid, and histopathological changes in the lung. To identify the mechanisms, IgE, IgG(1) and IgG(2a) in the serum were analysed and the CD25(+) Tregs in the mice were depleted with anti-CD25 monoclonal antibody (mAb). RESULTS: BCG and the transfer of BCG-stimulated DCs both suppressed all aspects of the asthmatic responses, namely, BHR, the production of total IgE and OVA-specific IgE and IgGs, and pulmonary eosinophilic inflammation. Anti-CD25mAb treatment reversed these effects. CONCLUSIONS: BCG can attenuate the allergic inflammation in a mouse model of asthma by a Tregs-related mechanism that is mediated by DCs. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2014-05 2013-08-23 /pmc/articles/PMC4021237/ /pubmed/24843794 http://dx.doi.org/10.4168/aair.2014.6.3.201 Text en Copyright © 2014 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Young-Joon
Kim, Ha-Jung
Kang, Mi-Jin
Yu, Ho-Sung
Seo, Ju-Hee
Kim, Hyung-Young
Park, Seoung-Ju
Lee, Yong-Chul
Hong, Soo-Jong
Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells
title Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells
title_full Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells
title_fullStr Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells
title_full_unstemmed Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells
title_short Bacillus Calmette-Guérin Suppresses Asthmatic Responses via CD4(+)CD25(+) Regulatory T Cells and Dendritic Cells
title_sort bacillus calmette-guérin suppresses asthmatic responses via cd4(+)cd25(+) regulatory t cells and dendritic cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021237/
https://www.ncbi.nlm.nih.gov/pubmed/24843794
http://dx.doi.org/10.4168/aair.2014.6.3.201
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