AbstractBackgroundAzithromycin treatment improves clinical parameters in patients with CF, and alters macrophage activation from a pro-inflammatory (M1) phenotype to a pro-fibrotic, alternatively activated (M2) phenotype. The transcriptional profile of cells from patients receiving azithromycin is unknown.MethodsGene expression in association with macrophage polarization, inflammation, and tissue remodeling was assessed from sputum samples collected from patients with CF. Transcriptional profiles and clinical characteristics, including azithromycin therapy, were compared.ResultsExpression of NOS2 and TNFα was decreased in subjects receiving azithromycin, whereas expression of M2-associated genes was unaffected. Principal component analysis ...
Non disponibileInduction of ATP Binding Cassette (ABC) proteins involved in the chloride transport h...
Anti-inflammatory properties of azithromycin (AZM) have been proposed as possible mechanisms of clin...
Lung damage in cystic fibrosis (CF) patients is determined by mucus accumulation, Pseudomonas aerugi...
AbstractBackgroundAzithromycin treatment improves clinical parameters in patients with CF, and alter...
Azithromycin is effective at controlling exaggerated inflammation and slowing the long-term decline ...
Azithromycin improves clinical outcomes in patients with cystic fibrosis (CF), specifically in patie...
Macrophages phagocyte pathogenic microorganisms and orchestrate immune responses by producing a vari...
Macrophages phagocyte pathogenic microorganisms and orchestrate immune responses by producing a vari...
Prolonged macrolide antibiotic therapy at low doses improves clinical outcome in patients affected w...
Cystic fibrosis is a hereditary disease caused by a mutation in the Cystic Fibrosis Transmembrane co...
Prolonged macrolide antibiotic therapy at low doses improves clinical outcome in patients affected w...
AbstractBackgroundBeneficial effects of azithromycin in cystic fibrosis (CF) have been reported, how...
Background: Beneficial effects of azithromycin in cystic fibrosis (CF) have been reported, however, ...
Abstract Background Inflammation plays a critical role in lung disease development and progression i...
BACKGROUND: Inflammation plays a critical role in lung disease development and progression in cystic...
Non disponibileInduction of ATP Binding Cassette (ABC) proteins involved in the chloride transport h...
Anti-inflammatory properties of azithromycin (AZM) have been proposed as possible mechanisms of clin...
Lung damage in cystic fibrosis (CF) patients is determined by mucus accumulation, Pseudomonas aerugi...
AbstractBackgroundAzithromycin treatment improves clinical parameters in patients with CF, and alter...
Azithromycin is effective at controlling exaggerated inflammation and slowing the long-term decline ...
Azithromycin improves clinical outcomes in patients with cystic fibrosis (CF), specifically in patie...
Macrophages phagocyte pathogenic microorganisms and orchestrate immune responses by producing a vari...
Macrophages phagocyte pathogenic microorganisms and orchestrate immune responses by producing a vari...
Prolonged macrolide antibiotic therapy at low doses improves clinical outcome in patients affected w...
Cystic fibrosis is a hereditary disease caused by a mutation in the Cystic Fibrosis Transmembrane co...
Prolonged macrolide antibiotic therapy at low doses improves clinical outcome in patients affected w...
AbstractBackgroundBeneficial effects of azithromycin in cystic fibrosis (CF) have been reported, how...
Background: Beneficial effects of azithromycin in cystic fibrosis (CF) have been reported, however, ...
Abstract Background Inflammation plays a critical role in lung disease development and progression i...
BACKGROUND: Inflammation plays a critical role in lung disease development and progression in cystic...
Non disponibileInduction of ATP Binding Cassette (ABC) proteins involved in the chloride transport h...
Anti-inflammatory properties of azithromycin (AZM) have been proposed as possible mechanisms of clin...
Lung damage in cystic fibrosis (CF) patients is determined by mucus accumulation, Pseudomonas aerugi...