Effects of azithromycin on bronchial remodeling in the natural model of severe neutrophilic asthma in horses

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Sophie Mainguy-Seers
Roxane Boivin
Sheila Pourali Dogaheh
Francis Beaudry
Pierre Hélie
Alvaro G. Bonilla
James G. Martin
Jean-Pierre Lavoie
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[1] Université de Montréal,Department of Clinical Sciences, Faculty of Veterinary Medicine
[2] Université de Montréal,Department of Veterinary Biomedical Sciences, Faculty of Veterinary Medicine
[3] Université de Montréal,Department of Pathology and Microbiology, Faculty of Veterinary Medicine
[4] McGill University,Meakins Christie Laboratories
[5] McGill University Health Center Research Institute,Laboratoire de Sciences Judiciaires Et de Médecine Légale
[6] Ministère de La Sécurité Publique,undefined
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Steroid resistance in asthma has been associated with neutrophilic inflammation and severe manifestations of the disease. Macrolide add-on therapy can improve the quality of life and the exacerbation rate in refractory cases, possibly with greater effectiveness in neutrophilic phenotypes. The mechanisms leading to these beneficial effects are incompletely understood and whether macrolides potentiate the modulation of bronchial remodeling induced by inhaled corticosteroids (ICS) is unknown. The objective of this study was to determine if adding azithromycin to ICS leads to further improvement of lung function, airway inflammation and bronchial remodeling in severe asthma. The combination of azithromycin (10 mg/kg q48h PO) and inhaled fluticasone (2500 µg q12h) was compared to the sole administration of fluticasone for five months in a randomized blind trial where the lung function, airway inflammation and bronchial remodeling (histomorphometry of central and peripheral airways and endobronchial ultrasound) of horses with severe neutrophilic asthma were assessed. Although the proportional reduction of airway neutrophilia was significantly larger in the group receiving azithromycin, the lung function and the peripheral and central airway smooth muscle mass decreased similarly in both groups. Despite a better control of airway neutrophilia, azithromycin did not potentiate the other clinical effects of fluticasone.
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