Enhanced activation of circulating plasmacytoid dendritic cells in patients with Chronic Obstructive Pulmonary Disease and experimental smoking-induced emphysema

Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and its role in smoking related-Chronic Obstructive Pulmonary Disease (COPD) remain largely unknown. The aim of this study was analyzed the phenot...

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Published inClinical immunology (Orlando, Fla.) Vol. 195; pp. 107 - 118
Main Authors Qiu, Shi-lin, Kuang, Liang-jian, Tang, Qi-ya, Duan, Min-chao, Bai, Jing, He, Zhi-yi, Zhang, Jian-quan, Li, Mei-hua, Deng, Jing-min, Liu, Guang-nan, Zhong, Xiao-ning
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LanguageEnglish
Published United States Elsevier Inc 01.10.2018
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Abstract Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and its role in smoking related-Chronic Obstructive Pulmonary Disease (COPD) remain largely unknown. The aim of this study was analyzed the phenotype of circulating pDCs and the expression of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells in patients with COPD by using multi-colour flow cytometry. The cytokine profiles in peripheral blood from all subjects were measured by ELISA. The influence of cigarette smoke on pDCs was evaluated in an experimental mouse model of emphysema. Circulating pDCs in patients with COPD and in mice exposed to cigarette smoke expressed high levels of co-stimulatory molecules CD40 or CD86 accompanied by exaggerated IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells. In vitro, cigarette smoke directly promoted pDCs maturation and release of IFN-α, IL-6 and IL-12, subsequently inducing differentiation of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells from mouse naïve CD8+T cells. These data suggested that circulating pDCs display an enhanced activation phenotype in patients with COPD and in experimental smoking mouse model of emphysema, which might contribute to exaggerated IFN-γ producing CD8+T and IL-17-producing CD8+T cell-mediated immune responses. •Circulating pDCs in patients with COPD and in experimental smoking mouse model of emphysema exhibited an enhanced activation phenotype.•IFN-γ producing CD8+T cells (Tc1) and IL-17-producing CD8+T cells (Tc17) both were exaggerated in patients with COPD and in mice exposed to cigarette smoke.•Cigarette smoke directly promoted pDCs maturation and the secretion of a series pro-inflammatory cytokine in vitro.•Cigarette smoke extract treated pDCs were sufficient to induced differentiation of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells by mouse naïve CD8+T cells in vitro.
AbstractList Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and its role in smoking related-Chronic Obstructive Pulmonary Disease (COPD) remain largely unknown. The aim of this study was analyzed the phenotype of circulating pDCs and the expression of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells in patients with COPD by using multi-colour flow cytometry. The cytokine profiles in peripheral blood from all subjects were measured by ELISA. The influence of cigarette smoke on pDCs was evaluated in an experimental mouse model of emphysema. Circulating pDCs in patients with COPD and in mice exposed to cigarette smoke expressed high levels of co-stimulatory molecules CD40 or CD86 accompanied by exaggerated IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells. In vitro, cigarette smoke directly promoted pDCs maturation and release of IFN-α, IL-6 and IL-12, subsequently inducing differentiation of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells from mouse naïve CD8+T cells. These data suggested that circulating pDCs display an enhanced activation phenotype in patients with COPD and in experimental smoking mouse model of emphysema, which might contribute to exaggerated IFN-γ producing CD8+T and IL-17-producing CD8+T cell-mediated immune responses. •Circulating pDCs in patients with COPD and in experimental smoking mouse model of emphysema exhibited an enhanced activation phenotype.•IFN-γ producing CD8+T cells (Tc1) and IL-17-producing CD8+T cells (Tc17) both were exaggerated in patients with COPD and in mice exposed to cigarette smoke.•Cigarette smoke directly promoted pDCs maturation and the secretion of a series pro-inflammatory cytokine in vitro.•Cigarette smoke extract treated pDCs were sufficient to induced differentiation of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells by mouse naïve CD8+T cells in vitro.
Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and its role in smoking related-Chronic Obstructive Pulmonary Disease (COPD) remain largely unknown. The aim of this study was analyzed the phenotype of circulating pDCs and the expression of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells in patients with COPD by using multi-colour flow cytometry. The cytokine profiles in peripheral blood from all subjects were measured by ELISA. The influence of cigarette smoke on pDCs was evaluated in an experimental mouse model of emphysema. Circulating pDCs in patients with COPD and in mice exposed to cigarette smoke expressed high levels of co-stimulatory molecules CD40 or CD86 accompanied by exaggerated IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells. In vitro, cigarette smoke directly promoted pDCs maturation and release of IFN-α, IL-6 and IL-12, subsequently inducing differentiation of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells from mouse naïve CD8+T cells. These data suggested that circulating pDCs display an enhanced activation phenotype in patients with COPD and in experimental smoking mouse model of emphysema, which might contribute to exaggerated IFN-γ producing CD8+T and IL-17-producing CD8+T cell-mediated immune responses.Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and its role in smoking related-Chronic Obstructive Pulmonary Disease (COPD) remain largely unknown. The aim of this study was analyzed the phenotype of circulating pDCs and the expression of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells in patients with COPD by using multi-colour flow cytometry. The cytokine profiles in peripheral blood from all subjects were measured by ELISA. The influence of cigarette smoke on pDCs was evaluated in an experimental mouse model of emphysema. Circulating pDCs in patients with COPD and in mice exposed to cigarette smoke expressed high levels of co-stimulatory molecules CD40 or CD86 accompanied by exaggerated IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells. In vitro, cigarette smoke directly promoted pDCs maturation and release of IFN-α, IL-6 and IL-12, subsequently inducing differentiation of IFN-γ producing CD8+T cells and IL-17-producing CD8+T cells from mouse naïve CD8+T cells. These data suggested that circulating pDCs display an enhanced activation phenotype in patients with COPD and in experimental smoking mouse model of emphysema, which might contribute to exaggerated IFN-γ producing CD8+T and IL-17-producing CD8+T cell-mediated immune responses.
Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and its role in smoking related-Chronic Obstructive Pulmonary Disease (COPD) remain largely unknown. The aim of this study was analyzed the phenotype of circulating pDCs and the expression of IFN-γ producing CD8 T cells and IL-17-producing CD8 T cells in patients with COPD by using multi-colour flow cytometry. The cytokine profiles in peripheral blood from all subjects were measured by ELISA. The influence of cigarette smoke on pDCs was evaluated in an experimental mouse model of emphysema. Circulating pDCs in patients with COPD and in mice exposed to cigarette smoke expressed high levels of co-stimulatory molecules CD40 or CD86 accompanied by exaggerated IFN-γ producing CD8 T cells and IL-17-producing CD8 T cells. In vitro, cigarette smoke directly promoted pDCs maturation and release of IFN-α, IL-6 and IL-12, subsequently inducing differentiation of IFN-γ producing CD8 T cells and IL-17-producing CD8 T cells from mouse naïve CD8 T cells. These data suggested that circulating pDCs display an enhanced activation phenotype in patients with COPD and in experimental smoking mouse model of emphysema, which might contribute to exaggerated IFN-γ producing CD8 T and IL-17-producing CD8 T cell-mediated immune responses.
Author Qiu, Shi-lin
Tang, Qi-ya
Kuang, Liang-jian
Duan, Min-chao
He, Zhi-yi
Li, Mei-hua
Liu, Guang-nan
Bai, Jing
Deng, Jing-min
Zhong, Xiao-ning
Zhang, Jian-quan
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  givenname: Mei-hua
  surname: Li
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  givenname: Jing-min
  surname: Deng
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  surname: Zhong
  fullname: Zhong, Xiao-ning
  email: xnzhong101@sina.com
  organization: Department of Respiratory Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29127016$$D View this record in MEDLINE/PubMed
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Keywords Smoking mouse model of emphysema
IL-17-producing CD8+T cells
IFN-γ producing CD8+T cells
Plasmacytoid dendritic cells(pDCs)
COPD
IL-17-producing CD8(+)T cells
IFN-γ producing CD8(+)T cells
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Snippet Plasmacytoid dendritic cells (pDCs) are key cells bridging the innate with adaptive immunity. However, the phenotypic characteristics of circulating pDCs and...
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SubjectTerms COPD
IFN-γ producing CD8+ T cells
IL-17-producing CD8+ T cells
Plasmacytoid dendritic cells(pDCs)
Smoking mouse model of emphysema
Title Enhanced activation of circulating plasmacytoid dendritic cells in patients with Chronic Obstructive Pulmonary Disease and experimental smoking-induced emphysema
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https://dx.doi.org/10.1016/j.clim.2017.11.003
https://www.ncbi.nlm.nih.gov/pubmed/29127016
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