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Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD

PURPOSE: This study aimed to measure the serum levels of interleukin (IL)-17, IL-10, and IL-35 in patients with stable chronic obstructive pulmonary disease (COPD) and disclose the correlations between their expression levels and clinical factors of patients. METHODS: A total of 75 patients with sta...

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Autores principales: Jiang, Shenghua, Shan, Fenglian, Zhang, Youwen, Jiang, Luning, Cheng, Zhaozhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108328/
https://www.ncbi.nlm.nih.gov/pubmed/30154651
http://dx.doi.org/10.2147/COPD.S167192
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author Jiang, Shenghua
Shan, Fenglian
Zhang, Youwen
Jiang, Luning
Cheng, Zhaozhong
author_facet Jiang, Shenghua
Shan, Fenglian
Zhang, Youwen
Jiang, Luning
Cheng, Zhaozhong
author_sort Jiang, Shenghua
collection PubMed
description PURPOSE: This study aimed to measure the serum levels of interleukin (IL)-17, IL-10, and IL-35 in patients with stable chronic obstructive pulmonary disease (COPD) and disclose the correlations between their expression levels and clinical factors of patients. METHODS: A total of 75 patients with stable COPD (47 males and 28 females) and 30 healthy controls (15 males and 15 females) were included in this study. The serum levels of IL-17, IL-10, and IL-35 were determined by enzyme-linked immunosorbent assay. The correlations between their expression levels and clinical factors of patients were determined using linear regression methods. RESULTS: The serum level of IL-17 was upregulated in stable COPD, and increased IL-17 expression was positively correlated with the Global Initiative for Chronic Obstructive Lung Disease (GOLD) grading, modified Medical Research Council (mMRC) score, and long clinical history (P<0.05), but negatively correlated with the pulmonary function (P<0.05) of patients. The serum levels of IL-10 and IL-35 were downregulated in stable COPD, and decreased IL-10 and IL-35 levels negatively correlated with the smoking status, GOLD grading, mMRC score, and long clinical history (P<0.05), but positively correlated with the pulmonary function (P<0.05) of patients. Moreover, the level of IL-17 negatively correlated with IL-10 and IL-35, but IL-10 positively correlated with IL-35. CONCLUSION: The serum levels of IL-17, IL-10, and IL-35 correlated with the clinical factors of COPD, indicating that they can serve as indicators to estimate the progression of COPD.
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spelling pubmed-61083282018-08-28 Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD Jiang, Shenghua Shan, Fenglian Zhang, Youwen Jiang, Luning Cheng, Zhaozhong Int J Chron Obstruct Pulmon Dis Original Research PURPOSE: This study aimed to measure the serum levels of interleukin (IL)-17, IL-10, and IL-35 in patients with stable chronic obstructive pulmonary disease (COPD) and disclose the correlations between their expression levels and clinical factors of patients. METHODS: A total of 75 patients with stable COPD (47 males and 28 females) and 30 healthy controls (15 males and 15 females) were included in this study. The serum levels of IL-17, IL-10, and IL-35 were determined by enzyme-linked immunosorbent assay. The correlations between their expression levels and clinical factors of patients were determined using linear regression methods. RESULTS: The serum level of IL-17 was upregulated in stable COPD, and increased IL-17 expression was positively correlated with the Global Initiative for Chronic Obstructive Lung Disease (GOLD) grading, modified Medical Research Council (mMRC) score, and long clinical history (P<0.05), but negatively correlated with the pulmonary function (P<0.05) of patients. The serum levels of IL-10 and IL-35 were downregulated in stable COPD, and decreased IL-10 and IL-35 levels negatively correlated with the smoking status, GOLD grading, mMRC score, and long clinical history (P<0.05), but positively correlated with the pulmonary function (P<0.05) of patients. Moreover, the level of IL-17 negatively correlated with IL-10 and IL-35, but IL-10 positively correlated with IL-35. CONCLUSION: The serum levels of IL-17, IL-10, and IL-35 correlated with the clinical factors of COPD, indicating that they can serve as indicators to estimate the progression of COPD. Dove Medical Press 2018-08-20 /pmc/articles/PMC6108328/ /pubmed/30154651 http://dx.doi.org/10.2147/COPD.S167192 Text en © 2018 Jiang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Jiang, Shenghua
Shan, Fenglian
Zhang, Youwen
Jiang, Luning
Cheng, Zhaozhong
Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD
title Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD
title_full Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD
title_fullStr Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD
title_full_unstemmed Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD
title_short Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD
title_sort increased serum il-17 and decreased serum il-10 and il-35 levels correlate with the progression of copd
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108328/
https://www.ncbi.nlm.nih.gov/pubmed/30154651
http://dx.doi.org/10.2147/COPD.S167192
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