Mutation-specific dual potentiators maximize rescue of CFTR gating mutants.
J Cyst Fibros
; 19(2): 236-244, 2020 03.
Article
en En
| MEDLINE
| ID: mdl-31678009
ABSTRACT
BACKGROUND:
The potentiator ivacaftor (VX-770) has been approved for therapy of 38 cystic fibrosis (CF) mutations (â¼10% of the patient population) associated with a gating defect of the CF transmembrane conductance regulator (CFTR). Despite the success of VX-770 treatment of patients carrying at least one allele of the most common gating mutation G551D-CFTR, some lung function decline and P. aeruginosa colonization persist. This study aims at identifying potentiator combinations that can considerably enhance the limited channel activity of a panel of CFTR gating mutants over monotherapy.METHODS:
The functional response of 13 CFTR mutants to single potentiators or systematic potentiator combinations was determined in the human bronchial epithelial cell line CFBE41o- and a subset of them was confirmed in primary human nasal epithelia (HNE).RESULTS:
In six out of thirteen CFTR missense mutants the fractional plasma membrane (PM) activity, a surrogate measure of CFTR channel gating, reached only â¼10-50% of WT channel activity upon VX-770 treatment, indicating incomplete gating correction. Combinatorial potentiator profiling and cluster analysis of mutant responses to 24 diverse investigational potentiators identified several compound pairs that improved the gating activity of R352Q-, S549R-, S549N-, G551D-, and G1244E-CFTR to â¼70-120% of the WT. Similarly, the potentiator combinations were able to confer WT-like function to G551D-CFTR in patient-derived human nasal epithelia.CONCLUSION:
This study suggests that half of CF patients with missense mutations approved for VX-770 administration, could benefit from the development of dual potentiator therapy.Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Piranos
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Pirazoles
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Transporte Iónico
/
Quinolonas
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Regulador de Conductancia de Transmembrana de Fibrosis Quística
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Fibrosis Quística
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Aminofenoles
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Mucosa Nasal
Límite:
Humans
Idioma:
En
Revista:
J Cyst Fibros
Año:
2020
Tipo del documento:
Article