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Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells

BACKGROUND: There have been few reports on the role of Fc receptors (FcRs) and immunoglobulin G (IgG) in asthma. The purpose of this study is to clarify the role of inhibitory FcRs and antigen presenting cells (APCs) in pathogenesis of asthma and to evaluate antigen-transporting and presenting capac...

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Autores principales: Ishikawa, Yumiko, Kobayashi, Kazuyuki, Yamamoto, Masatsugu, Nakata, Kyosuke, Takagawa, Tetsuya, Funada, Yasuhiro, Kotani, Yoshikazu, Karasuyama, Hajime, Yoshida, Masaru, Nishimura, Yoshihiro
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079623/
https://www.ncbi.nlm.nih.gov/pubmed/21477339
http://dx.doi.org/10.1186/1465-9921-12-42
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author Ishikawa, Yumiko
Kobayashi, Kazuyuki
Yamamoto, Masatsugu
Nakata, Kyosuke
Takagawa, Tetsuya
Funada, Yasuhiro
Kotani, Yoshikazu
Karasuyama, Hajime
Yoshida, Masaru
Nishimura, Yoshihiro
author_facet Ishikawa, Yumiko
Kobayashi, Kazuyuki
Yamamoto, Masatsugu
Nakata, Kyosuke
Takagawa, Tetsuya
Funada, Yasuhiro
Kotani, Yoshikazu
Karasuyama, Hajime
Yoshida, Masaru
Nishimura, Yoshihiro
author_sort Ishikawa, Yumiko
collection PubMed
description BACKGROUND: There have been few reports on the role of Fc receptors (FcRs) and immunoglobulin G (IgG) in asthma. The purpose of this study is to clarify the role of inhibitory FcRs and antigen presenting cells (APCs) in pathogenesis of asthma and to evaluate antigen-transporting and presenting capacity by APCs in the tracheobronchial mucosa. METHODS: In FcγRIIB deficient (KO) and C57BL/6 (WT) mice, the effects of intratracheal instillation of antigen-specific IgG were analysed using the model with sensitization and airborne challenge with ovalbumin (OVA). Thoracic lymph nodes instilled with fluorescein-conjugated OVA were analysed by fluorescence microscopy. Moreover, we analysed the CD11c(+ )MHC class II(+ )cells which intaken fluorescein-conjugated OVA in thoracic lymph nodes by flow cytometry. Also, lung-derived CD11c(+ )APCs were analysed by flow cytometry. Effects of anti-OVA IgG1 on bone marrow dendritic cells (BMDCs) in vitro were also analysed. Moreover, in FcγRIIB KO mice intravenously transplanted dendritic cells (DCs) differentiated from BMDCs of WT mice, the effects of intratracheal instillation of anti-OVA IgG were evaluated by bronchoalveolar lavage (BAL). RESULTS: In WT mice, total cells and eosinophils in BAL fluid reduced after instillation with anti-OVA IgG1. Anti-OVA IgG1 suppressed airway inflammation in hyperresponsiveness and histology. In addition, the number of the fluorescein-conjugated OVA in CD11c(+ )MHC class II(+ )cells of thoracic lymph nodes with anti-OVA IgG1 instillation decreased compared with PBS. Also, MHC class II expression on lung-derived CD11c(+ )APCs with anti-OVA IgG1 instillation reduced. Moreover, in vitro, we showed that BMDCs with anti-OVA IgG1 significantly decreased the T cell proliferation. Finally, we demonstrated that the lacking effects of anti-OVA IgG1 on airway inflammation on FcγRIIB KO mice were restored with WT-derived BMDCs transplanted intravenously. CONCLUSION: Antigen-specific IgG ameliorates allergic airway inflammation via FcγRIIB on DCs.
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spelling pubmed-30796232011-04-20 Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells Ishikawa, Yumiko Kobayashi, Kazuyuki Yamamoto, Masatsugu Nakata, Kyosuke Takagawa, Tetsuya Funada, Yasuhiro Kotani, Yoshikazu Karasuyama, Hajime Yoshida, Masaru Nishimura, Yoshihiro Respir Res Research BACKGROUND: There have been few reports on the role of Fc receptors (FcRs) and immunoglobulin G (IgG) in asthma. The purpose of this study is to clarify the role of inhibitory FcRs and antigen presenting cells (APCs) in pathogenesis of asthma and to evaluate antigen-transporting and presenting capacity by APCs in the tracheobronchial mucosa. METHODS: In FcγRIIB deficient (KO) and C57BL/6 (WT) mice, the effects of intratracheal instillation of antigen-specific IgG were analysed using the model with sensitization and airborne challenge with ovalbumin (OVA). Thoracic lymph nodes instilled with fluorescein-conjugated OVA were analysed by fluorescence microscopy. Moreover, we analysed the CD11c(+ )MHC class II(+ )cells which intaken fluorescein-conjugated OVA in thoracic lymph nodes by flow cytometry. Also, lung-derived CD11c(+ )APCs were analysed by flow cytometry. Effects of anti-OVA IgG1 on bone marrow dendritic cells (BMDCs) in vitro were also analysed. Moreover, in FcγRIIB KO mice intravenously transplanted dendritic cells (DCs) differentiated from BMDCs of WT mice, the effects of intratracheal instillation of anti-OVA IgG were evaluated by bronchoalveolar lavage (BAL). RESULTS: In WT mice, total cells and eosinophils in BAL fluid reduced after instillation with anti-OVA IgG1. Anti-OVA IgG1 suppressed airway inflammation in hyperresponsiveness and histology. In addition, the number of the fluorescein-conjugated OVA in CD11c(+ )MHC class II(+ )cells of thoracic lymph nodes with anti-OVA IgG1 instillation decreased compared with PBS. Also, MHC class II expression on lung-derived CD11c(+ )APCs with anti-OVA IgG1 instillation reduced. Moreover, in vitro, we showed that BMDCs with anti-OVA IgG1 significantly decreased the T cell proliferation. Finally, we demonstrated that the lacking effects of anti-OVA IgG1 on airway inflammation on FcγRIIB KO mice were restored with WT-derived BMDCs transplanted intravenously. CONCLUSION: Antigen-specific IgG ameliorates allergic airway inflammation via FcγRIIB on DCs. BioMed Central 2011 2011-04-10 /pmc/articles/PMC3079623/ /pubmed/21477339 http://dx.doi.org/10.1186/1465-9921-12-42 Text en Copyright ©2011 Ishikawa et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ishikawa, Yumiko
Kobayashi, Kazuyuki
Yamamoto, Masatsugu
Nakata, Kyosuke
Takagawa, Tetsuya
Funada, Yasuhiro
Kotani, Yoshikazu
Karasuyama, Hajime
Yoshida, Masaru
Nishimura, Yoshihiro
Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells
title Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells
title_full Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells
title_fullStr Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells
title_full_unstemmed Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells
title_short Antigen-Specific IgG ameliorates allergic airway inflammation via Fcγ receptor IIB on dendritic cells
title_sort antigen-specific igg ameliorates allergic airway inflammation via fcγ receptor iib on dendritic cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079623/
https://www.ncbi.nlm.nih.gov/pubmed/21477339
http://dx.doi.org/10.1186/1465-9921-12-42
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