Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers
- PMID: 28714611
- PMCID: PMC5664212
- DOI: 10.1002/ppul.23768
Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers
Abstract
Cystic fibrosis is characterized by an overly exuberant neutrophilic inflammatory response to pathogens and other stimuli that starts very early in disease. The overwhelming nature of this response is a primary cause of remodeling and destruction of the airways, suggesting that anti-inflammatory therapies could be beneficial in CF. However, finding therapies that can effectively reduce the inflammatory response without compromising host defenses remains elusive. New approaches towards mapping inflammatory targets promise to aid in developing novel therapeutic strategies and improve outcomes in individuals with CF.
Keywords: Sputum; bronchoalveolar lavage; exhaled breath condensate; metabolomics.
© 2017 Wiley Periodicals, Inc.
Conflict of interest statement
Conflicts of Interest: none declared
Figures
References
-
- Sly PD, Gangell CL, Chen L, Ware RS, Ranganathan S, Mott LS, Murray CP, Stick SM, Investigators AC. Risk factors for bronchiectasis in children with cystic fibrosis. N Engl J Med. 2013;368(21):1963–1970. - PubMed
-
- Montgomery ST, Mall MA, Kicic A, Stick SM, Arest CF. Hypoxia and sterile inflammation in cystic fibrosis airways: mechanisms and potential therapies. Eur Respir J. 2017;49(1) - PubMed
-
- Boucher RC. An overview of the pathogenesis of cystic fibrosis lung disease. Adv Drug Deliv Rev. 2002;54(11):1359–1371. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases