Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutrophilmediated tissue destruction, but its genesis and mechanisms remain poorly understood. To further define the pulmonary inflammatory response, we conducted a proteome-based screen of bronchoalveolar lavage fluid (BALF) collected from young children with and without CF experiencing endobronchial infection. Methods: We collected BALF samples from 45 children younger than 5 years and grouped them according to the presence of respiratory pathogens: >= 1 X 10(5) colony forming units (CFU)/mL BALF (18 and 12 samples with and without CF, respectively) an
Background: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammatio...
Summary. Background: The relationship between lower airway markers of inflammation and infection wit...
Copyright © 2019 by the American Thoracic Society. Rationale: Neutrophils are recruited to the airwa...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
(CF) is exaggerated and characterized by neutrophil-mediated tissue destruction, but its genesis and...
The immune landscape of the paediatric respiratory system remains largely uncharacterised and as a r...
Background: In adults with cystic fibrosis (CF), induced sputum (IS) is a minimally invasive alterna...
The pulmonary collectins surfactant protein (SP)-A and SP-D play important roles in innate lung defe...
The pulmonary collectins surfactant protein (SP)-A and SP-D play important roles in innate lung defe...
The pulmonary collectins surfactant protein (SP)-A and SP-D play important roles in innate lung defe...
Background: Cystic fibrosis (CF) lung disease begins in early life and is progressive with the major...
Background: We hypothesized that the inflammatory response in the lungs of children with cystic fibr...
Background: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammatio...
Summary. Background: The relationship between lower airway markers of inflammation and infection wit...
Copyright © 2019 by the American Thoracic Society. Rationale: Neutrophils are recruited to the airwa...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
Background: Airway inflammation in cystic fibrosis (CF) is exaggerated and characterized by neutroph...
(CF) is exaggerated and characterized by neutrophil-mediated tissue destruction, but its genesis and...
The immune landscape of the paediatric respiratory system remains largely uncharacterised and as a r...
Background: In adults with cystic fibrosis (CF), induced sputum (IS) is a minimally invasive alterna...
The pulmonary collectins surfactant protein (SP)-A and SP-D play important roles in innate lung defe...
The pulmonary collectins surfactant protein (SP)-A and SP-D play important roles in innate lung defe...
The pulmonary collectins surfactant protein (SP)-A and SP-D play important roles in innate lung defe...
Background: Cystic fibrosis (CF) lung disease begins in early life and is progressive with the major...
Background: We hypothesized that the inflammatory response in the lungs of children with cystic fibr...
Background: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammatio...
Summary. Background: The relationship between lower airway markers of inflammation and infection wit...
Copyright © 2019 by the American Thoracic Society. Rationale: Neutrophils are recruited to the airwa...