Neutrophil extracellular traps and interleukin-1β in cystic fibrosis lung disease

Cystic fibrosis (CF) lung disease manifests through abnormally thick mucus, persistent bacterial infections and a dysregulated innate immune system that involves significant neutrophilic inflammation. Neutrophils, immune cells essential to fight infections, accumulate in large numbers in CF airways...

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Bibliographic Details
Main Authors: Kayla M. Fantone, Naveen Gokanapudi, Balázs Rada
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1595994/full
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