Evidence for secondary ciliary dyskinesia in patients with cystic fibrosis.

Cilia Ciliary dyskinesia Cystic fibrosis Mucociliary clearance

Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
19 Oct 2024
Historique:
received: 18 01 2024
revised: 13 08 2024
accepted: 15 10 2024
medline: 21 10 2024
pubmed: 21 10 2024
entrez: 20 10 2024
Statut: aheadofprint

Résumé

Mucociliary clearance (MCC) impairment can be due to mucus abnormalities or to a ciliary dysfunction, which can be innate, or secondary to infection and/or inflammation. In cystic fibrosis (CF), it is well documented that MCC is impaired due to mucus abnormalities, but little is known concerning ciliary beating. This study aimed to confirm that ciliary dyskinesia is present in CF, and if this might be innate or secondary to the chronic infection and/or inflammation. Ciliated epithelial samples were obtained by nasal brushing from 51 CF patients, and from 30 healthy subjects. Ciliary beating was evaluated using digital high-speed videomicroscopy at 37 °C, allowing to evaluate ciliary beat frequency (CBF) and the percentage of abnormal beat pattern (CBP); this was repeated after air-liquid interface (ALI) cell culture. Ciliary dyskinesia was higher in CF patients than in healthy subjects, with a lower CBF and a higher percentage of abnormal CBP. Ciliary dyskinesia, already present in childhood, normalized after ALI cell culture. A chronic airway colonization did not worsen ciliary dyskinesia. We showed that, in CF, a ciliary dyskinesia, present from childhood, might contribute to the impaired MCC. Our results also found that the abnormal ciliary beating was not associated with a chronic infection, and resolved after ALI cell culture, suggesting that ciliary dyskinesia in CF is not innate, and might be secondary to chronic inflammation.

Sections du résumé

BACKGROUND BACKGROUND
Mucociliary clearance (MCC) impairment can be due to mucus abnormalities or to a ciliary dysfunction, which can be innate, or secondary to infection and/or inflammation. In cystic fibrosis (CF), it is well documented that MCC is impaired due to mucus abnormalities, but little is known concerning ciliary beating. This study aimed to confirm that ciliary dyskinesia is present in CF, and if this might be innate or secondary to the chronic infection and/or inflammation.
METHODS METHODS
Ciliated epithelial samples were obtained by nasal brushing from 51 CF patients, and from 30 healthy subjects. Ciliary beating was evaluated using digital high-speed videomicroscopy at 37 °C, allowing to evaluate ciliary beat frequency (CBF) and the percentage of abnormal beat pattern (CBP); this was repeated after air-liquid interface (ALI) cell culture.
RESULTS RESULTS
Ciliary dyskinesia was higher in CF patients than in healthy subjects, with a lower CBF and a higher percentage of abnormal CBP. Ciliary dyskinesia, already present in childhood, normalized after ALI cell culture. A chronic airway colonization did not worsen ciliary dyskinesia.
CONCLUSIONS CONCLUSIONS
We showed that, in CF, a ciliary dyskinesia, present from childhood, might contribute to the impaired MCC. Our results also found that the abnormal ciliary beating was not associated with a chronic infection, and resolved after ALI cell culture, suggesting that ciliary dyskinesia in CF is not innate, and might be secondary to chronic inflammation.

Identifiants

pubmed: 39428275
pii: S1569-1993(24)01796-X
doi: 10.1016/j.jcf.2024.10.003
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Anne-Lise Poirrier reports a relationship with GSK that includes: consulting or advisory and speaking and lecture fees. Anne-Lise Poirrier reports a relationship with Sanofi that includes: consulting or advisory and speaking and lecture fees. Renaud Louis reports a relationship with GSK that includes: consulting or advisory, funding grants, and speaking and lecture fees. Renaud Louis reports a relationship with AstraZeneca that includes: consulting or advisory, funding grants, and speaking and lecture fees. Renaud Louis reports a relationship with Chiesi that includes: funding grants and speaking and lecture fees. Florence Schleich reports a relationship with GSK that includes: consulting or advisory, funding grants. Florence Schleich reports a relationship with AstraZeneca that includes: consulting or advisory, funding grants. Florence Schleich reports a relationship with ALK that includes: consulting or advisory. Florence Schleich reports a relationship with Novartis that includes: consulting or advisory. Celine Kempeneers reports a relationship with Sanofi that includes: consulting or advisory.

Auteurs

Romane Bonhiver (R)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium; Division of Respirology, Department of Pediatrics, University Hospital of Liege, Belgium. Electronic address: rbonhiver@uliege.be.

Noemie Bricmont (N)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium; Division of Respirology, Department of Pediatrics, University Hospital of Liege, Belgium.

Maud Pirotte (M)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium.

Marc-Antoine Wuidart (MA)

Division of Physiotherapy, Regional Hospital Center of Liege, Belgium.

Justine Monseur (J)

Biostatistics and Research Method Center, Public Health Department, University of Liege, Belgium.

Lionel Benchimol (L)

Department of ENT, University Hospital Liege, Belgium.

Anne-Lise Poirrier (AL)

Department of ENT, University Hospital Liege, Belgium.

Catherine Moermans (C)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium; Department of Pneumology, University Hospital of Liege, Belgium.

Doriane Calmés (D)

Department of Pneumology, University Hospital of Liege, Belgium.

Florence Schleich (F)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium; Department of Pneumology, University Hospital of Liege, Belgium.

Renaud Louis (R)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium; Department of Pneumology, University Hospital of Liege, Belgium.

Marie-Christine Seghaye (MC)

Division of Cardiology, Department of Pediatrics, University Hospital Liege and University of Liege, Belgium.

Céline Kempeneers (C)

Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liege, Belgium; Division of Respirology, Department of Pediatrics, University Hospital of Liege, Belgium.

Classifications MeSH