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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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