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The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease

Viral infection is a common trigger for acute exacerbations of chronic obstructive pulmonary disease (AECOPD). The aim of this study is to investigate the expression of cytokines in AECOPD. Patients with AECOPD requiring hospitalization were recruited. Meanwhile healthy volunteers of similar age tha...

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Autores principales: Zheng, Jingtong, Shi, Yue, Xiong, Lingxin, Zhang, Weijie, Li, Ying, Gibson, Peter G., Simpson, Jodie L., Zhang, Chao, Lu, Junying, Sai, Jingying, Wang, Guoqiang, Wang, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352889/
https://www.ncbi.nlm.nih.gov/pubmed/28352642
http://dx.doi.org/10.1155/2017/8539294
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author Zheng, Jingtong
Shi, Yue
Xiong, Lingxin
Zhang, Weijie
Li, Ying
Gibson, Peter G.
Simpson, Jodie L.
Zhang, Chao
Lu, Junying
Sai, Jingying
Wang, Guoqiang
Wang, Fang
author_facet Zheng, Jingtong
Shi, Yue
Xiong, Lingxin
Zhang, Weijie
Li, Ying
Gibson, Peter G.
Simpson, Jodie L.
Zhang, Chao
Lu, Junying
Sai, Jingying
Wang, Guoqiang
Wang, Fang
author_sort Zheng, Jingtong
collection PubMed
description Viral infection is a common trigger for acute exacerbations of chronic obstructive pulmonary disease (AECOPD). The aim of this study is to investigate the expression of cytokines in AECOPD. Patients with AECOPD requiring hospitalization were recruited. Meanwhile healthy volunteers of similar age that accepted routine check-ups and showed no clinical symptoms of inflammatory diseases were also recruited. Induced sputum and serum were collected. Induced sputum of participants was processed and tested for thirteen viruses and bacteria. Forty cytokines were assayed in serum using the Quantibody Human Inflammation Array 3 (Ray Biotech, Inc.). The most common virus detected in virus positive AECOPD (VP) was influenza A (16%). No virus was found in controls. Circulating levels of IL-6, TNF-α, and MCP-1 were elevated in VP and coinfection subjects (p < 0.05), while the levels of 37 other cytokines showed no difference, compared with virus negative groups and controls (p > 0.05). Additionally, VP patients were less likely to have received influenza vaccination. VP patients had a systemic inflammation response involving IL-6, TNF-α, and MCP-1 which may be due to virus-induced activation of macrophages. There are important opportunities for further investigating AECOPD mechanisms and for the development of better strategies in the management and prevention of virus-related AECOPD.
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spelling pubmed-53528892017-03-28 The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease Zheng, Jingtong Shi, Yue Xiong, Lingxin Zhang, Weijie Li, Ying Gibson, Peter G. Simpson, Jodie L. Zhang, Chao Lu, Junying Sai, Jingying Wang, Guoqiang Wang, Fang J Immunol Res Research Article Viral infection is a common trigger for acute exacerbations of chronic obstructive pulmonary disease (AECOPD). The aim of this study is to investigate the expression of cytokines in AECOPD. Patients with AECOPD requiring hospitalization were recruited. Meanwhile healthy volunteers of similar age that accepted routine check-ups and showed no clinical symptoms of inflammatory diseases were also recruited. Induced sputum and serum were collected. Induced sputum of participants was processed and tested for thirteen viruses and bacteria. Forty cytokines were assayed in serum using the Quantibody Human Inflammation Array 3 (Ray Biotech, Inc.). The most common virus detected in virus positive AECOPD (VP) was influenza A (16%). No virus was found in controls. Circulating levels of IL-6, TNF-α, and MCP-1 were elevated in VP and coinfection subjects (p < 0.05), while the levels of 37 other cytokines showed no difference, compared with virus negative groups and controls (p > 0.05). Additionally, VP patients were less likely to have received influenza vaccination. VP patients had a systemic inflammation response involving IL-6, TNF-α, and MCP-1 which may be due to virus-induced activation of macrophages. There are important opportunities for further investigating AECOPD mechanisms and for the development of better strategies in the management and prevention of virus-related AECOPD. Hindawi 2017 2017-03-02 /pmc/articles/PMC5352889/ /pubmed/28352642 http://dx.doi.org/10.1155/2017/8539294 Text en Copyright © 2017 Jingtong Zheng et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zheng, Jingtong
Shi, Yue
Xiong, Lingxin
Zhang, Weijie
Li, Ying
Gibson, Peter G.
Simpson, Jodie L.
Zhang, Chao
Lu, Junying
Sai, Jingying
Wang, Guoqiang
Wang, Fang
The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease
title The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease
title_full The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease
title_fullStr The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease
title_full_unstemmed The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease
title_short The Expression of IL-6, TNF-α, and MCP-1 in Respiratory Viral Infection in Acute Exacerbations of Chronic Obstructive Pulmonary Disease
title_sort expression of il-6, tnf-α, and mcp-1 in respiratory viral infection in acute exacerbations of chronic obstructive pulmonary disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352889/
https://www.ncbi.nlm.nih.gov/pubmed/28352642
http://dx.doi.org/10.1155/2017/8539294
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