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Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases
BACKGROUND: Exposure to inhaled endotoxins (lipopolysaccharides, LPS) of Gram-negative bacteria commonly found in indoor environments and assessed in secondary tobacco smoke, has been associated with airway inflammation and asthma exacerbation. The bronchoalveolar lavage fluid (BALf) from patients w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551689/ https://www.ncbi.nlm.nih.gov/pubmed/23259971 http://dx.doi.org/10.1186/2049-6958-7-54 |
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author | Szponar, Bogumiła Larsson, Lennart Domagała-Kulawik, Joanna |
author_facet | Szponar, Bogumiła Larsson, Lennart Domagała-Kulawik, Joanna |
author_sort | Szponar, Bogumiła |
collection | PubMed |
description | BACKGROUND: Exposure to inhaled endotoxins (lipopolysaccharides, LPS) of Gram-negative bacteria commonly found in indoor environments and assessed in secondary tobacco smoke, has been associated with airway inflammation and asthma exacerbation. The bronchoalveolar lavage fluid (BALf) from patients with interstitial lung diseases (sarcoidosis, lung fibrosis, smoking-related ILD, eosinophilic disorders) was analyzed for the markers of lipopolysaccharide (LPS, endotoxin). METHODS: BALf was obtained from patients with diffuse lung diseases: idiopathic pulmonary fibrosis (n = 42), sarcoidosis (n = 22), smoking-related-ILD (n = 11) and eosinophilic disorders (n = 8). Total cell count and differential cell count were performed. In addition, samples were analyzed for 3-hydroxy fatty acids (3-OHFAs) of 10–18 carbon chain lengths, as markers of LPS, by gas chromatography-tandem mass spectrometry. RESULTS: The highest LPS concentration was found in patients with eosinophilic disorders and the lowest in patients with sarcoidosis (p< 0.05) followed by the lung fibrosis and the sr-ILD patients. The difference between LPS in BALf with extremely high eosinophil proportion (> 25%) and those with lower proportion was also significant (p = 0.014). A significant correlation was found between LPS and eosinophils, but not between LPS and lymphocytes, neutrophils, or macrophages count. CONCLUSIONS: A positive relationship of LPS and eosinophilic pulmonary disorders may be linked to a persistent eosinophil activation mediated by Th2 pathway: chronic endotoxin exposure would intensify Th2 pathway resulting in fibrosis and, at the same time, eosinophil stimulation, and hence in eosinophilic pulmonary disorders. |
format | Online Article Text |
id | pubmed-3551689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35516892013-01-24 Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases Szponar, Bogumiła Larsson, Lennart Domagała-Kulawik, Joanna Multidiscip Respir Med Original Research Article BACKGROUND: Exposure to inhaled endotoxins (lipopolysaccharides, LPS) of Gram-negative bacteria commonly found in indoor environments and assessed in secondary tobacco smoke, has been associated with airway inflammation and asthma exacerbation. The bronchoalveolar lavage fluid (BALf) from patients with interstitial lung diseases (sarcoidosis, lung fibrosis, smoking-related ILD, eosinophilic disorders) was analyzed for the markers of lipopolysaccharide (LPS, endotoxin). METHODS: BALf was obtained from patients with diffuse lung diseases: idiopathic pulmonary fibrosis (n = 42), sarcoidosis (n = 22), smoking-related-ILD (n = 11) and eosinophilic disorders (n = 8). Total cell count and differential cell count were performed. In addition, samples were analyzed for 3-hydroxy fatty acids (3-OHFAs) of 10–18 carbon chain lengths, as markers of LPS, by gas chromatography-tandem mass spectrometry. RESULTS: The highest LPS concentration was found in patients with eosinophilic disorders and the lowest in patients with sarcoidosis (p< 0.05) followed by the lung fibrosis and the sr-ILD patients. The difference between LPS in BALf with extremely high eosinophil proportion (> 25%) and those with lower proportion was also significant (p = 0.014). A significant correlation was found between LPS and eosinophils, but not between LPS and lymphocytes, neutrophils, or macrophages count. CONCLUSIONS: A positive relationship of LPS and eosinophilic pulmonary disorders may be linked to a persistent eosinophil activation mediated by Th2 pathway: chronic endotoxin exposure would intensify Th2 pathway resulting in fibrosis and, at the same time, eosinophil stimulation, and hence in eosinophilic pulmonary disorders. BioMed Central 2012-12-22 /pmc/articles/PMC3551689/ /pubmed/23259971 http://dx.doi.org/10.1186/2049-6958-7-54 Text en Copyright ©2012 Szponar 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 | Original Research Article Szponar, Bogumiła Larsson, Lennart Domagała-Kulawik, Joanna Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
title | Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
title_full | Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
title_fullStr | Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
title_full_unstemmed | Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
title_short | Endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
title_sort | endotoxin markers in bronchoalveolar lavage fluid of patients with interstitial lung diseases |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551689/ https://www.ncbi.nlm.nih.gov/pubmed/23259971 http://dx.doi.org/10.1186/2049-6958-7-54 |
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