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Updated: Oct 19, 2025

Forskolin-induced Swelling in Intestinal Organoids: An In Vitro Assay for Assessing Drug Response in Cystic Fibrosis Patients
Published on: February 11, 2017
CFTR modulator use in post lung transplant recipients.
Lauryn A Benninger1, Cesar Trillo1, Jorge Lascano1
1Department of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Florida College of Medicine, Gainesville, Florida.
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) modulator therapy, like Trikafta, shows promise in lung transplant recipients. This therapy may improve cystic fibrosis symptoms without negatively affecting lung transplant graft function or immunosuppression.
Area of Science:
- Pulmonology
- Transplant Surgery
- Pharmacology
Background:
- Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) modulator therapy was previously contraindicated in solid organ transplant recipients due to limited data and concerns about drug interactions.
- Potential benefits of CFTR modulators in improving extrapulmonary manifestations of cystic fibrosis in lung transplant recipients were unexplored.
Purpose of the Study:
- To evaluate the safety and efficacy of elexacaftor/tezacaftor/ivacaftor (Trikafta) in adult post-lung transplant recipients.
- To assess the impact of CFTR modulator therapy on graft function and immunosuppressive drug levels in this patient population.
Main Methods:
- Single-center retrospective study.
- Inclusion of adult patients who received lung transplants and were subsequently treated with elexacaftor/tezacaftor/ivacaftor.
- Monitoring of pulmonary function, extrapulmonary manifestations, graft function, and immunosuppressive drug levels.
Main Results:
- Elexacaftor/tezacaftor/ivacaftor treatment in post-lung transplant recipients was associated with improvements in extrapulmonary manifestations of cystic fibrosis.
- No significant negative impact on lung transplant graft function was observed.
- Immunosuppressive drug levels remained stable during CFTR modulator therapy.
Conclusions:
- CFTR modulator therapy, specifically elexacaftor/tezacaftor/ivacaftor, appears to be a viable option for managing cystic fibrosis in adult post-lung transplant recipients.
- This therapy may offer benefits for extrapulmonary symptoms without compromising graft integrity or immunosuppressive efficacy.
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