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Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice
Emerging evidence suggests that autoimmune processes are implicated in the pathogenesis of chronic obstructive pulmonary disease (COPD). In this study, we assessed the expression of B‐cell activating factor (BAFF) in smokers, and investigated the functional importance of BAFF in the induction and ma...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210376/ https://www.ncbi.nlm.nih.gov/pubmed/28039405 http://dx.doi.org/10.14814/phy2.13057 |
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author | Morissette, Mathieu C. Gao, Yang Shen, Pamela Thayaparan, Danya Bérubé, Jean‐Christophe Paré, Peter D. Brandsma, Corry‐Anke Hao, Ke Bossé, Yohan Ettinger, Rachel Herbst, Ronald Humbles, Alison A. Kolbeck, Roland Zhong, Nanshan Chen, Rongchang Stämpfli, Martin R. |
author_facet | Morissette, Mathieu C. Gao, Yang Shen, Pamela Thayaparan, Danya Bérubé, Jean‐Christophe Paré, Peter D. Brandsma, Corry‐Anke Hao, Ke Bossé, Yohan Ettinger, Rachel Herbst, Ronald Humbles, Alison A. Kolbeck, Roland Zhong, Nanshan Chen, Rongchang Stämpfli, Martin R. |
author_sort | Morissette, Mathieu C. |
collection | PubMed |
description | Emerging evidence suggests that autoimmune processes are implicated in the pathogenesis of chronic obstructive pulmonary disease (COPD). In this study, we assessed the expression of B‐cell activating factor (BAFF) in smokers, and investigated the functional importance of BAFF in the induction and maintenance of cigarette smoke‐induced pulmonary antinuclear antibodies (ANA) and tertiary lymphoid tissues (TLTs) using a preclinical mouse model. We observed that BAFF levels were elevated in smokers and mice exposed to cigarette smoke. In mice, BAFF expression was rapidly induced in the lungs following 4 days of cigarette smoke exposure and remained elevated following 8 and 24 weeks of exposure. Alveolar macrophages were the major source of BAFF. Blockade of BAFF using a BAFF receptor‐Fc (BAFFR‐Fc) construct prevented pulmonary ANA and TLT formation when delivered concurrent with cigarette smoke exposure. Under these conditions, no impact on lung inflammation was observed. However, administration of BAFFR‐Fc following smoking cessation markedly reduced the number of TLTs and ANA levels and, of note, reduced pulmonary neutrophilia. Altogether, this study shows for the first time a central role of BAFF in the induction and maintenance of cigarette smoke‐induced pulmonary ANA and suggests that BAFF blockade following smoking cessation could have beneficial effects on persistent inflammatory processes. In this study, we assessed the expression of B‐cell activating factor (BAFF) in smokers, and investigated the functional importance of BAFF in the induction and maintenance of cigarette smoke‐induced pulmonary antinuclear antibodies (ANA) and tertiary lymphoid tissues (TLTs) using a preclinical mouse model. Data presented show that BAFF plays a central role in the induction and maintenance of cigarette smoke‐induced pulmonary ANA and suggest a therapeutic potential for BAFF blockade in limiting autoimmune processes associated with smoking. |
format | Online Article Text |
id | pubmed-5210376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52103762017-01-05 Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice Morissette, Mathieu C. Gao, Yang Shen, Pamela Thayaparan, Danya Bérubé, Jean‐Christophe Paré, Peter D. Brandsma, Corry‐Anke Hao, Ke Bossé, Yohan Ettinger, Rachel Herbst, Ronald Humbles, Alison A. Kolbeck, Roland Zhong, Nanshan Chen, Rongchang Stämpfli, Martin R. Physiol Rep Original Research Emerging evidence suggests that autoimmune processes are implicated in the pathogenesis of chronic obstructive pulmonary disease (COPD). In this study, we assessed the expression of B‐cell activating factor (BAFF) in smokers, and investigated the functional importance of BAFF in the induction and maintenance of cigarette smoke‐induced pulmonary antinuclear antibodies (ANA) and tertiary lymphoid tissues (TLTs) using a preclinical mouse model. We observed that BAFF levels were elevated in smokers and mice exposed to cigarette smoke. In mice, BAFF expression was rapidly induced in the lungs following 4 days of cigarette smoke exposure and remained elevated following 8 and 24 weeks of exposure. Alveolar macrophages were the major source of BAFF. Blockade of BAFF using a BAFF receptor‐Fc (BAFFR‐Fc) construct prevented pulmonary ANA and TLT formation when delivered concurrent with cigarette smoke exposure. Under these conditions, no impact on lung inflammation was observed. However, administration of BAFFR‐Fc following smoking cessation markedly reduced the number of TLTs and ANA levels and, of note, reduced pulmonary neutrophilia. Altogether, this study shows for the first time a central role of BAFF in the induction and maintenance of cigarette smoke‐induced pulmonary ANA and suggests that BAFF blockade following smoking cessation could have beneficial effects on persistent inflammatory processes. In this study, we assessed the expression of B‐cell activating factor (BAFF) in smokers, and investigated the functional importance of BAFF in the induction and maintenance of cigarette smoke‐induced pulmonary antinuclear antibodies (ANA) and tertiary lymphoid tissues (TLTs) using a preclinical mouse model. Data presented show that BAFF plays a central role in the induction and maintenance of cigarette smoke‐induced pulmonary ANA and suggest a therapeutic potential for BAFF blockade in limiting autoimmune processes associated with smoking. John Wiley and Sons Inc. 2016-12-30 /pmc/articles/PMC5210376/ /pubmed/28039405 http://dx.doi.org/10.14814/phy2.13057 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Morissette, Mathieu C. Gao, Yang Shen, Pamela Thayaparan, Danya Bérubé, Jean‐Christophe Paré, Peter D. Brandsma, Corry‐Anke Hao, Ke Bossé, Yohan Ettinger, Rachel Herbst, Ronald Humbles, Alison A. Kolbeck, Roland Zhong, Nanshan Chen, Rongchang Stämpfli, Martin R. Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
title | Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
title_full | Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
title_fullStr | Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
title_full_unstemmed | Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
title_short | Role of BAFF in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
title_sort | role of baff in pulmonary autoantibody responses induced by chronic cigarette smoke exposure in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210376/ https://www.ncbi.nlm.nih.gov/pubmed/28039405 http://dx.doi.org/10.14814/phy2.13057 |
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