Targeted mRNA restoration of ciliary function in DNAI1-related primary ciliary dyskinesia: ex vivo rescue in patient-derived nasal spheroids—a proof-of-concept study
Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by impaired ciliary function, defective mucociliary clearance, and progressive lung disease. Pathogenic variants in the DNAI1 gene are a well-known cause of PCD. Currently, no approved therapies address the underlying genetic defect. RCT1100 is an inhaled mRNA therapy encoding DNAI1 currently under clinical development. This proof-of-concept study aims to evaluate the functional effects of RCT1100 in a rapid three-dimensional explant spheroid (3DE-S) model comprising apical-out, primary nasal epithelial cells derived from patients with DNAI1-PCD. 3DE-S were generated from nasal brushings of five patients with confirmed biallelic disease causing variants in DNAI1 . RCT1100 was administered from day 5 directly to culture wells three times weekly for 2 weeks. Spheroid motility was assessed throughout treatment by quantifying the proportion of moving spheroid rolling and their movement speed. Following six doses, spheroids were harvested for high-speed video microscopy for assessment of ciliary beat frequency. Evaluable data were obtained from three of five patient samples: two samples were excluded one due to contamination and one as a result of technical difficulties when producing videos for high-speed video microscopy. After six doses of RCT1100, ciliary beat frequency increased from a baseline range of 2.8–3.5 Hz to 6.7–6.8 Hz ( p = 0.033) postharvesting. Mean spheroid movement speed increased from 0.11 µm/s to 3.87 µm/s ( p = 0.0002) following dosing with 10 µg/mL RCT1100, with more than 80% of spheroids exhibiting coordinated rolling motion pattern. The 3DE-S model provides a feasible platform for assessing targeted therapies in PCD. In this proof-of-concept study, RCT1100 was associated with functional improvements in DNAI1-derived spheroids, warranting further investigation in larger studies and supporting the use of spheroid-based systems as translational tools for precision medicine in PCD. Trial registration EU Clinical Trials Register [EUCTR]: 2023–510521-14-00, ClinicalTrials.gov ID: NCT06633757, registration date 07-oct-2024.
Authors
- Caroline Marie Torp Nygaard (ORCID: https://orcid.org/0009-0007-0837-7979)
- Cristian Herrera-Cid (ORCID: https://orcid.org/0000-0002-2010-4785)
- Jessica A. Couch (ORCID: https://orcid.org/0009-0005-6605-1809)
- Laura Nedergaard (ORCID: https://orcid.org/0009-0000-4387-5008)
- S G Johansen
- Tavs Qvist
- June Kehlet Marthin
- John G. Matthews
- Søren Tvorup Christensen
- Kim G. Nielsen
Institutions
- University of Copenhagen (DK)
- Copenhagen University Hospital (DK)
- Rigshospitalet (DK)
- Vyne Therapeutics (United States) (US)
Publication Details
- Journal
- European journal of medical research
- Published
- 2026-10-13
- DOI
- https://doi.org/10.1186/s40001-026-05313-9
- Primary Topic
- Cystic Fibrosis Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 0.00