| Literature DB >> 28714611 |
Olivia Giddings1,2,3, Charles R Esther2,3.
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.Entities:
Keywords: Sputum; bronchoalveolar lavage; exhaled breath condensate; metabolomics
Mesh:
Substances:
Year: 2017 PMID: 28714611 PMCID: PMC5664212 DOI: 10.1002/ppul.23768
Source DB: PubMed Journal: Pediatr Pulmonol ISSN: 1099-0496