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• W2058742845 abstract "Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR), a channel that normally transports anions across epithelial cell membranes. The most common manifestation of CF is buildup of mucus in the airways and bacterial colonization of the lower respiratory tract, accompanied by chronic inflammation. Antibiotics are used to control CF-associated opportunistic infections, but lengthy antibiotic treatment risks the emergence of multiple-drug resistant (MDR) strains. New antimicrobial strategies are needed to prevent and treat infections in these high-risk individuals. Autophagy contributes to the control of a variety of microbial infections. For this reason, the recent discovery of functional impairment of autophagy in CF provides a new basis for understanding susceptibility to severe infections. Here, we review the role of autophagy in host defense against CF-associated bacterial and fungal pathogens, and survey pharmacologic approaches to restore normal autophagy function in these individuals. Autophagy restoration therapy may improve pathogen clearance and mitigate lung inflammation in CF airways." @default.
• W2058742845 created "2016-06-24" @default.
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• W2058742845 creator A5029808150 @default.
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• W2058742845 date "2014-01-13" @default.
• W2058742845 modified "2023-10-17" @default.
• W2058742845 title "The emerging potential of autophagy-based therapies in the treatment of cystic fibrosis lung infections" @default.
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• W2058742845 doi "https://doi.org/10.4161/auto.27750" @default.
• W2058742845 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4077897" @default.
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