News

Mucus Defect in CF Found to Be Present at Birth Could Spur On New Treatments

People suffering from Cystic Fibrosis (CF) usually develop lung disease due to a defective host defense that allows bacterial infections in the airways. Furthermore, advanced CF patients cannot preform mucociliary transport (MCT), a process that traps and drives bacteria from the lungs through mucus flows in the epithelium…

New X-Ray “Blueprint” of Pseudomonas Aeruginosa May Lead To New Cystic Fibrosis Therapies

Pseudomonas Aeruginosa is a complex, formidable bacterial infection that is notoriously difficult to treat, particularly in patients with lowered immune response and who have Cystic Fibrosis. While the bacteria’s mode of operation, which involves targeting and infecting damaged tissue, is relatively well understood, the method by which Pseudomonas Aeruginosa adapts to…