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Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function

BACKGROUND: Inhaled corticosteroid use is associated with increased rates of pneumonia in COPD patients. The underlying mechanism is unknown, although recent data suggest that pneumonia is more frequent in patients treated with fluticasone propionate (FP) than budesonide. Macrophages and neutrophils...

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Autores principales: Belchamber, Kylie BR, Thomas, Catherine MR, Dunne, Amy E, Barnes, Peter J, Donnelly, Louise E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147211/
https://www.ncbi.nlm.nih.gov/pubmed/30271135
http://dx.doi.org/10.2147/COPD.S169337
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author Belchamber, Kylie BR
Thomas, Catherine MR
Dunne, Amy E
Barnes, Peter J
Donnelly, Louise E
author_facet Belchamber, Kylie BR
Thomas, Catherine MR
Dunne, Amy E
Barnes, Peter J
Donnelly, Louise E
author_sort Belchamber, Kylie BR
collection PubMed
description BACKGROUND: Inhaled corticosteroid use is associated with increased rates of pneumonia in COPD patients. The underlying mechanism is unknown, although recent data suggest that pneumonia is more frequent in patients treated with fluticasone propionate (FP) than budesonide. Macrophages and neutrophils from COPD patients are deficient in clearing bacteria, and this might explain increased bacterial colonization in COPD. Inhaled corticosteroid may further suppress this response; therefore, we examined the effect of FP and budesonide on phagocytosis of common respiratory pathogens by monocyte-derived macrophages (MDMs) and neutrophils. METHODS: MDMs from COPD patients (n=20–24) were preincubated with FP or budesonide for 1 or 18 hours, after which phagocytosis of fluorescently labeled inert beads or heat-killed Haemophilus influenzae/Streptococcus pneumoniae were measured fluorimetrically after 1 or 4 hours. Additionally, CXCL8, IL6, and TNFα concentrations in supernatants by ELISA, MDM-scavenger-receptor expression by flow cytometry, and MDM ability to kill bacteria were measured. Neutrophils from COPD patients (n=8) were preincubated with corticosteroids for 1 hour and bacteria phagocytosis measured by flow cytometry. RESULTS: After 1 hour’s preincubation, neither corticosteroid altered MDM phagocytosis of beads or H. influenzae; however, budesonide (10(−7) M) increased S. pneumoniae phagocytosis by 23% (P<0.05). After 18 hours’ preincubation, neither corticosteroid altered MDM phagocytosis of any prey, although H. influenzae phagocytosis by budesonide was significantly greater compared to FP at 10(−6) and 10(−5) M (P<0.05). The 1-hour preincubation with either corticosteroid inhibited bacteria-induced CXCL8 release (at 10(−7) and 10(−5) M, P<0.05); however, this effect was lost at 18-hour preincubation. There was no change in receptor expression, bacterial killing, or neutrophil phagocytosis by either corticosteroid. CONCLUSION: These data suggest that dissolved FP and budesonide do not have an overall effect on MDM or neutrophil phagocytosis of bacteria.
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spelling pubmed-61472112018-09-28 Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function Belchamber, Kylie BR Thomas, Catherine MR Dunne, Amy E Barnes, Peter J Donnelly, Louise E Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Inhaled corticosteroid use is associated with increased rates of pneumonia in COPD patients. The underlying mechanism is unknown, although recent data suggest that pneumonia is more frequent in patients treated with fluticasone propionate (FP) than budesonide. Macrophages and neutrophils from COPD patients are deficient in clearing bacteria, and this might explain increased bacterial colonization in COPD. Inhaled corticosteroid may further suppress this response; therefore, we examined the effect of FP and budesonide on phagocytosis of common respiratory pathogens by monocyte-derived macrophages (MDMs) and neutrophils. METHODS: MDMs from COPD patients (n=20–24) were preincubated with FP or budesonide for 1 or 18 hours, after which phagocytosis of fluorescently labeled inert beads or heat-killed Haemophilus influenzae/Streptococcus pneumoniae were measured fluorimetrically after 1 or 4 hours. Additionally, CXCL8, IL6, and TNFα concentrations in supernatants by ELISA, MDM-scavenger-receptor expression by flow cytometry, and MDM ability to kill bacteria were measured. Neutrophils from COPD patients (n=8) were preincubated with corticosteroids for 1 hour and bacteria phagocytosis measured by flow cytometry. RESULTS: After 1 hour’s preincubation, neither corticosteroid altered MDM phagocytosis of beads or H. influenzae; however, budesonide (10(−7) M) increased S. pneumoniae phagocytosis by 23% (P<0.05). After 18 hours’ preincubation, neither corticosteroid altered MDM phagocytosis of any prey, although H. influenzae phagocytosis by budesonide was significantly greater compared to FP at 10(−6) and 10(−5) M (P<0.05). The 1-hour preincubation with either corticosteroid inhibited bacteria-induced CXCL8 release (at 10(−7) and 10(−5) M, P<0.05); however, this effect was lost at 18-hour preincubation. There was no change in receptor expression, bacterial killing, or neutrophil phagocytosis by either corticosteroid. CONCLUSION: These data suggest that dissolved FP and budesonide do not have an overall effect on MDM or neutrophil phagocytosis of bacteria. Dove Medical Press 2018-09-17 /pmc/articles/PMC6147211/ /pubmed/30271135 http://dx.doi.org/10.2147/COPD.S169337 Text en © 2018 Belchamber et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Belchamber, Kylie BR
Thomas, Catherine MR
Dunne, Amy E
Barnes, Peter J
Donnelly, Louise E
Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function
title Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function
title_full Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function
title_fullStr Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function
title_full_unstemmed Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function
title_short Comparison of fluticasone propionate and budesonide on COPD macrophage and neutrophil function
title_sort comparison of fluticasone propionate and budesonide on copd macrophage and neutrophil function
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147211/
https://www.ncbi.nlm.nih.gov/pubmed/30271135
http://dx.doi.org/10.2147/COPD.S169337
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