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Nasal airway inflammatory responses and pathogen detection in infants with cystic fibrosis.

Authors :
Kopp BT
Ross SE
Bojja D
Guglani L
Chandler JD
Tirouvanziam R
Thompson M
Slaven JE
Chmiel JF
Siracusa C
Sanders DB
Source :
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society [J Cyst Fibros] 2024 Mar; Vol. 23 (2), pp. 219-225. Date of Electronic Publication: 2023 Nov 15.
Publication Year :
2024

Abstract

Background: Detecting airway inflammation non-invasively in infants with cystic fibrosis (CF) is difficult. We hypothesized that markers of inflammation in CF [IL-1β, IL-6, IL-8, IL-10, IL-17A, neutrophil elastase (NE) and tumor necrosis factor (TNF-α)] could be measured in infants with CF from nasal fluid and would be elevated during viral infections or clinician-defined pulmonary exacerbations (PEx).<br />Methods: We collected nasal fluid, nasal swabs, and hair samples from 34 infants with CF during monthly clinic visits, sick visits, and hospitalizations. Nasal fluid was isolated and analyzed for cytokines. Respiratory viral detection on nasal swabs was performed using the Luminex NxTAG® Respiratory Pathogen Panel. Hair samples were analyzed for nicotine concentration by reverse-phase high-performance liquid chromatography. We compared nasal cytokine concentrations between the presence and absence of detected respiratory viruses, PEx, and smoke exposure.<br />Results: A total of 246 samples were analyzed. Compared to measurements in the absence of respiratory viruses, mean concentrations of IL-6, IL-8, TNF-α, and NE were significantly increased while IL-17A was significantly decreased in infants positive for respiratory viruses. IL-17A was significantly decreased and NE increased in those with a PEx. IL-8 and NE were significantly increased in infants with enteric pathogen positivity on airway cultures, but not P. aeruginosa or S. aureus. Compared to those with no smoke exposure, there were significantly higher levels of IL-6, IL-10, and NE in infants with detectable levels of nicotine.<br />Conclusions: Noninvasive collection of nasal fluid may identify inflammation in infants with CF during changing clinical or environmental exposures.<br />Competing Interests: Declaration of Competing Interest The authors have no declarations of interest.<br /> (Copyright © 2023 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-5010
Volume :
23
Issue :
2
Database :
MEDLINE
Journal :
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Publication Type :
Academic Journal
Accession number :
37977937
Full Text :
https://doi.org/10.1016/j.jcf.2023.10.020