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Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD
BACKGROUND: The link between long-term ICS therapy and respiratory infection in COPD patients is controversial. We investigated the effect of long-term use of inhaled corticosteroid on Toll like receptor 2 (TLR2) expression in induced sputum from COPD patients. METHODS: 51 patients were divided into...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733430/ https://www.ncbi.nlm.nih.gov/pubmed/27234389 http://dx.doi.org/10.1186/2213-0802-1-7 |
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author | Zhu, Haixing Shi, Yuheng Tang, Wei Shi, Guocao Wan, Huanyin |
author_facet | Zhu, Haixing Shi, Yuheng Tang, Wei Shi, Guocao Wan, Huanyin |
author_sort | Zhu, Haixing |
collection | PubMed |
description | BACKGROUND: The link between long-term ICS therapy and respiratory infection in COPD patients is controversial. We investigated the effect of long-term use of inhaled corticosteroid on Toll like receptor 2 (TLR2) expression in induced sputum from COPD patients. METHODS: 51 patients were divided into two groups according to their treatment history: long-term ICS treatment group (patients who have used ICS (equivalent to Fluticasone Propionate (FP) ≥ 500 ug/day for more than 1 year) (n = 21) and ICS naive group (who have never routinely used ICS before, n = 29). In their induced sputum, we tested TLR2 extracellular and intracellular expression on macrophages using flowcytometry. TLR2 and tumor necrosis factor αmRNA expression were also evaluated by real-time PCR. RESULTS: TLR2 extracellular expression on the macrophages from induced sputum in long-term ICS treatment group was lower than the ICS naïve group (13.69% ± 1.17% vs 20.12% ± 4.37%, p = 0.019). TLR2 intracellular expression in the macrophages, the TLR2 and TNFαmRNA in the induced sputum also showed a trend towards decreased endpoint in ICS long-term treatment group compare to ICS naïve group but did not reach significance. TLR2 extracellular and TLR2 intracellular expression were strongly related (r = 0.645, p = P = 0.017) as well as TNFαmRNA and TLR2 mRNA expression (r = 0.894, p = 0.0001). CONCLUSION: Long-term use of ICS may have negative influence on TLR2 expression in the airway of severe COPD patient. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2213-0802-1-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6733430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-67334302019-09-09 Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD Zhu, Haixing Shi, Yuheng Tang, Wei Shi, Guocao Wan, Huanyin Transl Respir Med Research BACKGROUND: The link between long-term ICS therapy and respiratory infection in COPD patients is controversial. We investigated the effect of long-term use of inhaled corticosteroid on Toll like receptor 2 (TLR2) expression in induced sputum from COPD patients. METHODS: 51 patients were divided into two groups according to their treatment history: long-term ICS treatment group (patients who have used ICS (equivalent to Fluticasone Propionate (FP) ≥ 500 ug/day for more than 1 year) (n = 21) and ICS naive group (who have never routinely used ICS before, n = 29). In their induced sputum, we tested TLR2 extracellular and intracellular expression on macrophages using flowcytometry. TLR2 and tumor necrosis factor αmRNA expression were also evaluated by real-time PCR. RESULTS: TLR2 extracellular expression on the macrophages from induced sputum in long-term ICS treatment group was lower than the ICS naïve group (13.69% ± 1.17% vs 20.12% ± 4.37%, p = 0.019). TLR2 intracellular expression in the macrophages, the TLR2 and TNFαmRNA in the induced sputum also showed a trend towards decreased endpoint in ICS long-term treatment group compare to ICS naïve group but did not reach significance. TLR2 extracellular and TLR2 intracellular expression were strongly related (r = 0.645, p = P = 0.017) as well as TNFαmRNA and TLR2 mRNA expression (r = 0.894, p = 0.0001). CONCLUSION: Long-term use of ICS may have negative influence on TLR2 expression in the airway of severe COPD patient. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2213-0802-1-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-03-19 /pmc/articles/PMC6733430/ /pubmed/27234389 http://dx.doi.org/10.1186/2213-0802-1-7 Text en © Zhu et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. 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 Zhu, Haixing Shi, Yuheng Tang, Wei Shi, Guocao Wan, Huanyin Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD |
title | Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD |
title_full | Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD |
title_fullStr | Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD |
title_full_unstemmed | Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD |
title_short | Inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with COPD |
title_sort | inhaled corticosteroid influence toll like receptor 2 expression in induced sputum from patients with copd |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733430/ https://www.ncbi.nlm.nih.gov/pubmed/27234389 http://dx.doi.org/10.1186/2213-0802-1-7 |
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