BACKGROUND: It is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF) has an influence on circulating polymorphonuclear neutrophil (PMN) function and apoptosis. PATIENTS AND METHODS: Blood PMNs were obtained from 14 CF patients before and after antibiotic treatment for an acute exacerbation, and from 10 healthy controls. PMNs were evaluated for production of reactive oxygen species (ROS) by spectrophotometry, of cytokines in the conditioned medium by ELISA, and apoptotic response by cytofluorimetry. RESULTS: ROS and interleukin (IL)-8 were produced at higher levels by CF PMNs pre-therapy than control PMNs under basal conditions. IL-8 levels further increased after therapy. Early apoptotic response was higher i...
BACKGROUND: Early in life, patients with cystic fibrosis (CF) are infected with microorganisms inclu...
AbstractBackgroundChronic Pseudomonas aeruginosa lung infection is the major reason for premature de...
The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has no...
BACKGROUND: It is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF) has...
BACKGROUND: It is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF) has...
AbstractBackgroundIt is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF...
Background and objective: In cystic fibrosis (CF) very few studies have assessed sputum 8-iso-PGF2 ...
It is not known whether cytokine levels in sputum may be used as outocome measures after parenteral ...
In seeking more specific biomarkers of the cystic fibrosis (CF) lung inflammatory disease that would...
<div><p>In seeking more specific biomarkers of the cystic fibrosis (CF) lung inflammatory disease th...
The thesis investigates reasons for a failure of neutrophils to clear pulmonary bacterial infection ...
Background-The aim of this study was to compare neutrophil migration in cystic fibrosis (CF) and non...
BACKGROUND: The focus of this study was to characterize a novel biomarker for cystic fibrosis (CF) t...
To the Editor: Cystic fibrosis (CF) is the most common life-shortening genetic disorder in the Cauc...
Various treatment regimens and difficulties with research design are encountered with cystic fibrosi...
BACKGROUND: Early in life, patients with cystic fibrosis (CF) are infected with microorganisms inclu...
AbstractBackgroundChronic Pseudomonas aeruginosa lung infection is the major reason for premature de...
The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has no...
BACKGROUND: It is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF) has...
BACKGROUND: It is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF) has...
AbstractBackgroundIt is not known whether antibiotic therapy for lung disease in cystic fibrosis (CF...
Background and objective: In cystic fibrosis (CF) very few studies have assessed sputum 8-iso-PGF2 ...
It is not known whether cytokine levels in sputum may be used as outocome measures after parenteral ...
In seeking more specific biomarkers of the cystic fibrosis (CF) lung inflammatory disease that would...
<div><p>In seeking more specific biomarkers of the cystic fibrosis (CF) lung inflammatory disease th...
The thesis investigates reasons for a failure of neutrophils to clear pulmonary bacterial infection ...
Background-The aim of this study was to compare neutrophil migration in cystic fibrosis (CF) and non...
BACKGROUND: The focus of this study was to characterize a novel biomarker for cystic fibrosis (CF) t...
To the Editor: Cystic fibrosis (CF) is the most common life-shortening genetic disorder in the Cauc...
Various treatment regimens and difficulties with research design are encountered with cystic fibrosi...
BACKGROUND: Early in life, patients with cystic fibrosis (CF) are infected with microorganisms inclu...
AbstractBackgroundChronic Pseudomonas aeruginosa lung infection is the major reason for premature de...
The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has no...