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The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers

BACKGROUND: An association between innate immunity including Toll-like receptors (TLRs) and COPD is reported recently; TLR4 deficiency in lung can cause emphysema in animals, which is not evident in humans. We analyzed the association of TLR4 expression, airflow limitation and emphysema in smokers....

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Autores principales: Lee, Sei Won, Kim, Dal Rae, Kim, Tae Jung, Paik, Jin Ho, Chung, Jin-Haeng, Jheon, Sanghoon, Huh, Jin Won, Lee, Jae-Ho, Lee, Choon-Taek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546871/
https://www.ncbi.nlm.nih.gov/pubmed/23170858
http://dx.doi.org/10.1186/1465-9921-13-106
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author Lee, Sei Won
Kim, Dal Rae
Kim, Tae Jung
Paik, Jin Ho
Chung, Jin-Haeng
Jheon, Sanghoon
Huh, Jin Won
Lee, Jae-Ho
Lee, Choon-Taek
author_facet Lee, Sei Won
Kim, Dal Rae
Kim, Tae Jung
Paik, Jin Ho
Chung, Jin-Haeng
Jheon, Sanghoon
Huh, Jin Won
Lee, Jae-Ho
Lee, Choon-Taek
author_sort Lee, Sei Won
collection PubMed
description BACKGROUND: An association between innate immunity including Toll-like receptors (TLRs) and COPD is reported recently; TLR4 deficiency in lung can cause emphysema in animals, which is not evident in humans. We analyzed the association of TLR4 expression, airflow limitation and emphysema in smokers. METHODS: We enrolled patients of ≥40years old with smoking histories of ≥10 pack-years and who had undergone lung resection. We measured TLR4 expression in lung lysates. The severity of emphysema was evaluated on computed tomography. TLR4 expression was also evaluated immunohistochemically. RESULTS: In total, 53 patients were enrolled. Forced expiratory volume in one second per forced vital capacity (FEV(1)/FVC) increased (P=0.03) and emphysema score decreased (P=0.01) as TLR4 expression increased. These were still significant, in multiple regression analysis including sex, age, tuberculosis history, smoking history and inhaled corticosteroid (ICS) usage. We also classified patients as high, intermediate, and low expressers according to TLR4 expression. Although no differences in age, gender, tuberculosis, or smoking history were observed among the groups, emphysema severity increased significantly (P = 0.02) and FEV(1)/FVC decreased significantly (P = 0.006) in TLR4 low expresser. The difference in TLR4 expression based on immunohistochemistry was most prominent in bronchial and alveolar epithelial cells. CONCLUSION: Down-regulated TLR4 expression in lung was associated with emphysema and airflow limitation in smokers.
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spelling pubmed-35468712013-01-17 The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers Lee, Sei Won Kim, Dal Rae Kim, Tae Jung Paik, Jin Ho Chung, Jin-Haeng Jheon, Sanghoon Huh, Jin Won Lee, Jae-Ho Lee, Choon-Taek Respir Res Research BACKGROUND: An association between innate immunity including Toll-like receptors (TLRs) and COPD is reported recently; TLR4 deficiency in lung can cause emphysema in animals, which is not evident in humans. We analyzed the association of TLR4 expression, airflow limitation and emphysema in smokers. METHODS: We enrolled patients of ≥40years old with smoking histories of ≥10 pack-years and who had undergone lung resection. We measured TLR4 expression in lung lysates. The severity of emphysema was evaluated on computed tomography. TLR4 expression was also evaluated immunohistochemically. RESULTS: In total, 53 patients were enrolled. Forced expiratory volume in one second per forced vital capacity (FEV(1)/FVC) increased (P=0.03) and emphysema score decreased (P=0.01) as TLR4 expression increased. These were still significant, in multiple regression analysis including sex, age, tuberculosis history, smoking history and inhaled corticosteroid (ICS) usage. We also classified patients as high, intermediate, and low expressers according to TLR4 expression. Although no differences in age, gender, tuberculosis, or smoking history were observed among the groups, emphysema severity increased significantly (P = 0.02) and FEV(1)/FVC decreased significantly (P = 0.006) in TLR4 low expresser. The difference in TLR4 expression based on immunohistochemistry was most prominent in bronchial and alveolar epithelial cells. CONCLUSION: Down-regulated TLR4 expression in lung was associated with emphysema and airflow limitation in smokers. BioMed Central 2012 2012-11-21 /pmc/articles/PMC3546871/ /pubmed/23170858 http://dx.doi.org/10.1186/1465-9921-13-106 Text en Copyright ©2012 Lee 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
Lee, Sei Won
Kim, Dal Rae
Kim, Tae Jung
Paik, Jin Ho
Chung, Jin-Haeng
Jheon, Sanghoon
Huh, Jin Won
Lee, Jae-Ho
Lee, Choon-Taek
The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
title The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
title_full The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
title_fullStr The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
title_full_unstemmed The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
title_short The association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
title_sort association of down-regulated toll-like receptor 4 expression with airflow limitation and emphysema in smokers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546871/
https://www.ncbi.nlm.nih.gov/pubmed/23170858
http://dx.doi.org/10.1186/1465-9921-13-106
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