The Detection of Bile Acids in the Lungs of Paediatric Cystic Fibrosis Patients Is Associated with Altered Inflammatory Patterns

<i>Background</i>: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammation and recurrent airway infections play major roles in the initiation and progression of the disease. Little is known about triggering factors modulating the transition to chronic mi...

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Bibliographic Details
Main Authors: Jose A. Caparrós-Martín, Stephanie Flynn, F. Jerry Reen, David F. Woods, Patricia Agudelo-Romero, Sarath C. Ranganathan, Stephen M. Stick, Fergal O’Gara
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/10/5/282