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Impaired macrophage phagocytosis of bacteria in severe asthma

BACKGROUND: Bacteria are frequently cultured from sputum samples of severe asthma patients suggesting a defect in bacterial clearance from the airway. We measured the capacity of macrophages from patients with asthma to phagocytose bacteria. METHODS: Phagocytosis of fluorescently-labelled polystyren...

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Autores principales: Liang, Zhike, Zhang, Qingling, Thomas, Catherine MR, Chana, Kirandeep K, Gibeon, David, Barnes, Peter J, Chung, Kian Fan, Bhavsar, Pankaj K, Donnelly, Louise E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086996/
https://www.ncbi.nlm.nih.gov/pubmed/24972601
http://dx.doi.org/10.1186/1465-9921-15-72
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author Liang, Zhike
Zhang, Qingling
Thomas, Catherine MR
Chana, Kirandeep K
Gibeon, David
Barnes, Peter J
Chung, Kian Fan
Bhavsar, Pankaj K
Donnelly, Louise E
author_facet Liang, Zhike
Zhang, Qingling
Thomas, Catherine MR
Chana, Kirandeep K
Gibeon, David
Barnes, Peter J
Chung, Kian Fan
Bhavsar, Pankaj K
Donnelly, Louise E
author_sort Liang, Zhike
collection PubMed
description BACKGROUND: Bacteria are frequently cultured from sputum samples of severe asthma patients suggesting a defect in bacterial clearance from the airway. We measured the capacity of macrophages from patients with asthma to phagocytose bacteria. METHODS: Phagocytosis of fluorescently-labelled polystyrene beads, Haemophilus influenzae or Staphylococcus aureus by broncholaveolar lavage alveolar macrophages (AM) and by monocyte-derived macrophages (MDM) from non-asthmatics, mild-moderate and severe asthmatic patients was assessed using fluorimetry. RESULTS: There were no differences in phagocytosis of polystyrene beads by AMs or MDMs from any of the subject groups. There was reduced phagocytosis of Haemophilus influenzae and Staphylococcus aureus in MDMs from patients with severe asthma compared to non-severe asthma (p < 0.05 and p < 0.01, respectively) and healthy subjects (p < 0.01and p < 0.001, respectively). Phagocytosis of Haemophilus influenzae and Staphylococcus aureus by AM was also reduced in severe asthma compared to normal subjects (p < 0.05). Dexamethasone and formoterol did not suppress phagocytosis of bacteria by MDMs from any of the groups. CONCLUSIONS: Persistence of bacteria in the lower airways may result partly from a reduced phagocytic capacity of macrophages for bacteria. This may contribute to increased exacerbations, airway colonization and persistence of inflammation.
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spelling pubmed-40869962014-07-09 Impaired macrophage phagocytosis of bacteria in severe asthma Liang, Zhike Zhang, Qingling Thomas, Catherine MR Chana, Kirandeep K Gibeon, David Barnes, Peter J Chung, Kian Fan Bhavsar, Pankaj K Donnelly, Louise E Respir Res Research BACKGROUND: Bacteria are frequently cultured from sputum samples of severe asthma patients suggesting a defect in bacterial clearance from the airway. We measured the capacity of macrophages from patients with asthma to phagocytose bacteria. METHODS: Phagocytosis of fluorescently-labelled polystyrene beads, Haemophilus influenzae or Staphylococcus aureus by broncholaveolar lavage alveolar macrophages (AM) and by monocyte-derived macrophages (MDM) from non-asthmatics, mild-moderate and severe asthmatic patients was assessed using fluorimetry. RESULTS: There were no differences in phagocytosis of polystyrene beads by AMs or MDMs from any of the subject groups. There was reduced phagocytosis of Haemophilus influenzae and Staphylococcus aureus in MDMs from patients with severe asthma compared to non-severe asthma (p < 0.05 and p < 0.01, respectively) and healthy subjects (p < 0.01and p < 0.001, respectively). Phagocytosis of Haemophilus influenzae and Staphylococcus aureus by AM was also reduced in severe asthma compared to normal subjects (p < 0.05). Dexamethasone and formoterol did not suppress phagocytosis of bacteria by MDMs from any of the groups. CONCLUSIONS: Persistence of bacteria in the lower airways may result partly from a reduced phagocytic capacity of macrophages for bacteria. This may contribute to increased exacerbations, airway colonization and persistence of inflammation. BioMed Central 2014 2014-06-27 /pmc/articles/PMC4086996/ /pubmed/24972601 http://dx.doi.org/10.1186/1465-9921-15-72 Text en Copyright © 2014 Liang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 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
Liang, Zhike
Zhang, Qingling
Thomas, Catherine MR
Chana, Kirandeep K
Gibeon, David
Barnes, Peter J
Chung, Kian Fan
Bhavsar, Pankaj K
Donnelly, Louise E
Impaired macrophage phagocytosis of bacteria in severe asthma
title Impaired macrophage phagocytosis of bacteria in severe asthma
title_full Impaired macrophage phagocytosis of bacteria in severe asthma
title_fullStr Impaired macrophage phagocytosis of bacteria in severe asthma
title_full_unstemmed Impaired macrophage phagocytosis of bacteria in severe asthma
title_short Impaired macrophage phagocytosis of bacteria in severe asthma
title_sort impaired macrophage phagocytosis of bacteria in severe asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086996/
https://www.ncbi.nlm.nih.gov/pubmed/24972601
http://dx.doi.org/10.1186/1465-9921-15-72
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