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Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma
Background and Objective: Airway macrophages perform the crucial functions of presenting antigens, clearing pathogens, and apoptotic cells. Macrophage phagocytosis is increased in adults with mild asthma and allergen exposure is known to activate macrophages. However, it is not clear whether the mec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082964/ https://www.ncbi.nlm.nih.gov/pubmed/30116724 http://dx.doi.org/10.3389/fped.2018.00206 |
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author | Kulkarni, Neeta Kantar, Ahmad Costella, Silvia Ragazzo, Vincenzo Piacentini, Giorgio Boner, Attilio O'Callaghan, Christopher |
author_facet | Kulkarni, Neeta Kantar, Ahmad Costella, Silvia Ragazzo, Vincenzo Piacentini, Giorgio Boner, Attilio O'Callaghan, Christopher |
author_sort | Kulkarni, Neeta |
collection | PubMed |
description | Background and Objective: Airway macrophages perform the crucial functions of presenting antigens, clearing pathogens, and apoptotic cells. Macrophage phagocytosis is increased in adults with mild asthma and allergen exposure is known to activate macrophages. However, it is not clear whether the mechanism behind this is due to a primary defect or environmental factors such as allergen or lipopolysaccaride (LPS) exposure. Our aim was to assess the phagocytic function of airway macrophages in children with mild to moderate asthma after residence in a low allergen\LPS environment at high altitude. Methods: Sputum induction was performed in children with asthma at baseline and after residence for a 3 weeks' period at a high-altitude asthma center that has very low ambient allergen levels. The markers of eosinophilic inflammation (including percentage of macrophage cytoplasm with red hue) and phagocytosis of fluorescein isothiocyanate-labeled, heat-killed Staphylococcus aureus by airway macrophages was analyzed. Internalized bacteria were quantified using confocal microscopy. Results: The median bacterial count [mean (standard deviation)] per macrophage was significantly lower [39.55 (4.51) vs. 73.26 (39.42) (p = 0.006)] after residence at high altitude. No association was observed between markers of eosinophilic inflammation and bacterial phagocytosis. Conclusions: The results suggest that the mechanism behind the enhanced phagocytosis of bacteria in childhood asthma may be secondary to allergen or possibly LPS exposure. |
format | Online Article Text |
id | pubmed-6082964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60829642018-08-16 Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma Kulkarni, Neeta Kantar, Ahmad Costella, Silvia Ragazzo, Vincenzo Piacentini, Giorgio Boner, Attilio O'Callaghan, Christopher Front Pediatr Pediatrics Background and Objective: Airway macrophages perform the crucial functions of presenting antigens, clearing pathogens, and apoptotic cells. Macrophage phagocytosis is increased in adults with mild asthma and allergen exposure is known to activate macrophages. However, it is not clear whether the mechanism behind this is due to a primary defect or environmental factors such as allergen or lipopolysaccaride (LPS) exposure. Our aim was to assess the phagocytic function of airway macrophages in children with mild to moderate asthma after residence in a low allergen\LPS environment at high altitude. Methods: Sputum induction was performed in children with asthma at baseline and after residence for a 3 weeks' period at a high-altitude asthma center that has very low ambient allergen levels. The markers of eosinophilic inflammation (including percentage of macrophage cytoplasm with red hue) and phagocytosis of fluorescein isothiocyanate-labeled, heat-killed Staphylococcus aureus by airway macrophages was analyzed. Internalized bacteria were quantified using confocal microscopy. Results: The median bacterial count [mean (standard deviation)] per macrophage was significantly lower [39.55 (4.51) vs. 73.26 (39.42) (p = 0.006)] after residence at high altitude. No association was observed between markers of eosinophilic inflammation and bacterial phagocytosis. Conclusions: The results suggest that the mechanism behind the enhanced phagocytosis of bacteria in childhood asthma may be secondary to allergen or possibly LPS exposure. Frontiers Media S.A. 2018-08-02 /pmc/articles/PMC6082964/ /pubmed/30116724 http://dx.doi.org/10.3389/fped.2018.00206 Text en Copyright © 2018 Kulkarni, Kantar, Costella, Ragazzo, Piacentini, Boner and O'Callaghan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Kulkarni, Neeta Kantar, Ahmad Costella, Silvia Ragazzo, Vincenzo Piacentini, Giorgio Boner, Attilio O'Callaghan, Christopher Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma |
title | Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma |
title_full | Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma |
title_fullStr | Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma |
title_full_unstemmed | Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma |
title_short | Macrophage Phagocytosis and Allergen Avoidance in Children With Asthma |
title_sort | macrophage phagocytosis and allergen avoidance in children with asthma |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082964/ https://www.ncbi.nlm.nih.gov/pubmed/30116724 http://dx.doi.org/10.3389/fped.2018.00206 |
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