Background: Chronic lung infection with Pseudomonas aeruginosa remains a major cause of mortality and morbidity among individuals with CF. Expression of mediators promoting recruitment and differentiation of B cells, or supporting antibody production is poorly understood yet could be key to controlling infection. Methods: BAFF was measured in BAL from children with CF, both with and without P. aeruginosa, and controls. Mice were intra-nasally infected with P. aeruginosa strain LESB65 for up to 7 days. Cellular infiltration and expression of B cell chemoattractants and B cell differentiation factor, BAFF were measured in lung tissue. Results: BAFF expression was elevated in both P. aeruginosa negative and positive CF patients and in P. aerug...
The patients with Cystic Fibrosis (CF), an inherent genetic disorder, suffer from chronic bacterial ...
International audienceBACKGROUND: Lungs of cystic fibrosis (CF) patients are chronically infected wi...
Lung disease is the major cause of mortality in cystic fibrosis patients. Lack of functional cystic ...
Background: Chronic lung infection with Pseudomonas aeruginosa remains a major cause of mortality an...
<div><p>Background</p><p>Chronic lung infection with <i>Pseudomonas aeruginosa</i> remains a major c...
Background Chronic lung infection with Pseudomonas aeruginosa remains a major cause of mortality and...
Rationale: Cystic fibrosis (CF) is characterized by progressive pulmonary inflammation that is infec...
Objectives: CF is characterized by loss of pulmonary function and tissue injury. As the disease prog...
Rationale: B cell-activating factor (BAFF) plays a major role in activation of B cells and in adapti...
Repeated cycles of infections, caused mainly by Pseudomonas aeruginosa, combined with a robust host ...
Studies in cystic fibrosis patients have suggested that the balance between pro- and anti-inflammato...
The number of LFs, BAFF+, TLR4+ and proliferation marker Ki67+ B cells in lung explants or resection...
B cells, key cells in allergic inflammation, differentiate in the bone marrow and their precursors i...
Pseudomonas aeruginosa is the leading cause of morbidity and mortality in cystic fibrosis (CF). This...
International audienceBackground and AimsIn cystic fibrosis (CF), Pseudomonas aeruginosa is not erad...
The patients with Cystic Fibrosis (CF), an inherent genetic disorder, suffer from chronic bacterial ...
International audienceBACKGROUND: Lungs of cystic fibrosis (CF) patients are chronically infected wi...
Lung disease is the major cause of mortality in cystic fibrosis patients. Lack of functional cystic ...
Background: Chronic lung infection with Pseudomonas aeruginosa remains a major cause of mortality an...
<div><p>Background</p><p>Chronic lung infection with <i>Pseudomonas aeruginosa</i> remains a major c...
Background Chronic lung infection with Pseudomonas aeruginosa remains a major cause of mortality and...
Rationale: Cystic fibrosis (CF) is characterized by progressive pulmonary inflammation that is infec...
Objectives: CF is characterized by loss of pulmonary function and tissue injury. As the disease prog...
Rationale: B cell-activating factor (BAFF) plays a major role in activation of B cells and in adapti...
Repeated cycles of infections, caused mainly by Pseudomonas aeruginosa, combined with a robust host ...
Studies in cystic fibrosis patients have suggested that the balance between pro- and anti-inflammato...
The number of LFs, BAFF+, TLR4+ and proliferation marker Ki67+ B cells in lung explants or resection...
B cells, key cells in allergic inflammation, differentiate in the bone marrow and their precursors i...
Pseudomonas aeruginosa is the leading cause of morbidity and mortality in cystic fibrosis (CF). This...
International audienceBackground and AimsIn cystic fibrosis (CF), Pseudomonas aeruginosa is not erad...
The patients with Cystic Fibrosis (CF), an inherent genetic disorder, suffer from chronic bacterial ...
International audienceBACKGROUND: Lungs of cystic fibrosis (CF) patients are chronically infected wi...
Lung disease is the major cause of mortality in cystic fibrosis patients. Lack of functional cystic ...