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Compartment differences of inflammatory activity in chronic obstructive pulmonary disease

BACKGROUND: Chronic obstructive pulmonary disease (COPD) is associated with local and systemic inflammation. The knowledge of interaction and co-variation of the inflammatory responses in different compartments is meagre. METHOD: Healthy controls (n = 23), smokers with (n = 28) and without (n = 29)...

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Autores principales: Ji, Jie, von Schéele, Ida, Bergström, Jan, Billing, Bo, Dahlén, Barbro, Lantz, Ann-Sofie, Larsson, Kjell, Palmberg, Lena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243731/
https://www.ncbi.nlm.nih.gov/pubmed/25155252
http://dx.doi.org/10.1186/s12931-014-0104-3
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author Ji, Jie
von Schéele, Ida
Bergström, Jan
Billing, Bo
Dahlén, Barbro
Lantz, Ann-Sofie
Larsson, Kjell
Palmberg, Lena
author_facet Ji, Jie
von Schéele, Ida
Bergström, Jan
Billing, Bo
Dahlén, Barbro
Lantz, Ann-Sofie
Larsson, Kjell
Palmberg, Lena
author_sort Ji, Jie
collection PubMed
description BACKGROUND: Chronic obstructive pulmonary disease (COPD) is associated with local and systemic inflammation. The knowledge of interaction and co-variation of the inflammatory responses in different compartments is meagre. METHOD: Healthy controls (n = 23), smokers with (n = 28) and without (n = 29) COPD performed spirometry and dental examinations. Saliva, induced sputum, bronchoalveolar lavage (BAL) fluid and serum were collected. Inflammatory markers were assessed in all compartments using ELISA, flow cytometry and RT-PCR. RESULTS: Negative correlations between lung function and saliva IL-8 and matrix metalloproteinase-9 (MMP-9) were found in smokers with COPD. IL-8 and MMP-9 in saliva correlated positively with periodontal disease as assessed by gingival bleeding in non-smokers. Tumor necrosis factor-α (TNF-α) in saliva, serum and TNF-α mRNA expression on macrophages in BAL-fluid were lower in smokers than in non-smokers. There were positive correlations between soluble TNF-α receptor 1 (sTNFR1) and soluble TNF-α receptor 2 (sTNFR2) in sputum, BAL-fluid and serum in all groups. Sputum interleukin-8 (IL-8) or interleukin-6 (IL-6) was positively correlated with sTNFR1 or sTNFR2 in non-smokers and with sTNFR2 in COPD. CONCLUSION: Saliva which is convenient to collect and analyse, may be suitable for biomarker assessment of disease activity in COPD. An attenuated TNF-α expression was demonstrated by both protein and mRNA analyses in different compartments suggesting that TNF-α response is altered in moderate and severe COPD. Shedding of TNFR1 or TNFR2 is similarly regulated irrespective of airflow limitation.
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spelling pubmed-42437312014-11-26 Compartment differences of inflammatory activity in chronic obstructive pulmonary disease Ji, Jie von Schéele, Ida Bergström, Jan Billing, Bo Dahlén, Barbro Lantz, Ann-Sofie Larsson, Kjell Palmberg, Lena Respir Res Research BACKGROUND: Chronic obstructive pulmonary disease (COPD) is associated with local and systemic inflammation. The knowledge of interaction and co-variation of the inflammatory responses in different compartments is meagre. METHOD: Healthy controls (n = 23), smokers with (n = 28) and without (n = 29) COPD performed spirometry and dental examinations. Saliva, induced sputum, bronchoalveolar lavage (BAL) fluid and serum were collected. Inflammatory markers were assessed in all compartments using ELISA, flow cytometry and RT-PCR. RESULTS: Negative correlations between lung function and saliva IL-8 and matrix metalloproteinase-9 (MMP-9) were found in smokers with COPD. IL-8 and MMP-9 in saliva correlated positively with periodontal disease as assessed by gingival bleeding in non-smokers. Tumor necrosis factor-α (TNF-α) in saliva, serum and TNF-α mRNA expression on macrophages in BAL-fluid were lower in smokers than in non-smokers. There were positive correlations between soluble TNF-α receptor 1 (sTNFR1) and soluble TNF-α receptor 2 (sTNFR2) in sputum, BAL-fluid and serum in all groups. Sputum interleukin-8 (IL-8) or interleukin-6 (IL-6) was positively correlated with sTNFR1 or sTNFR2 in non-smokers and with sTNFR2 in COPD. CONCLUSION: Saliva which is convenient to collect and analyse, may be suitable for biomarker assessment of disease activity in COPD. An attenuated TNF-α expression was demonstrated by both protein and mRNA analyses in different compartments suggesting that TNF-α response is altered in moderate and severe COPD. Shedding of TNFR1 or TNFR2 is similarly regulated irrespective of airflow limitation. BioMed Central 2014-08-26 2014 /pmc/articles/PMC4243731/ /pubmed/25155252 http://dx.doi.org/10.1186/s12931-014-0104-3 Text en © Ji et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ji, Jie
von Schéele, Ida
Bergström, Jan
Billing, Bo
Dahlén, Barbro
Lantz, Ann-Sofie
Larsson, Kjell
Palmberg, Lena
Compartment differences of inflammatory activity in chronic obstructive pulmonary disease
title Compartment differences of inflammatory activity in chronic obstructive pulmonary disease
title_full Compartment differences of inflammatory activity in chronic obstructive pulmonary disease
title_fullStr Compartment differences of inflammatory activity in chronic obstructive pulmonary disease
title_full_unstemmed Compartment differences of inflammatory activity in chronic obstructive pulmonary disease
title_short Compartment differences of inflammatory activity in chronic obstructive pulmonary disease
title_sort compartment differences of inflammatory activity in chronic obstructive pulmonary disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243731/
https://www.ncbi.nlm.nih.gov/pubmed/25155252
http://dx.doi.org/10.1186/s12931-014-0104-3
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