“…CF mucus is more adherent, viscous, dehydrated, and impairs normal mucociliary escalator clearance [1,4,9,10,16,17,28,30,32,40,42,[49][50][51]. Alterations in, and macromolecular complexity of, CF secretions create physical and chemical barriers to the immune system, to regional ventilation, to antibiotic and mucolytic agents, and to potential gene therapy vehicles [4,37,48,50,[52][53][54][55][56]. CF mucus is a rich mixture of plasma proteins, inflammatory cells, DNA, bacteria, and bacterial products, with alveolar and tracheobronchial epithelial and submucosal gland secretions.…”