4.3 Article

Ivacaftor potentiation of multiple CFTR channels with gating mutations

Journal

JOURNAL OF CYSTIC FIBROSIS
Volume 11, Issue 3, Pages 237-245

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jcf.2011.12.005

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Background: The investigational CFTR potentiator ivacaftor (VX-770) increased CFTR channel activity and improved lung function in subjects with CF who have the 055 ID CFTR gating mutation. The aim of this in vitro study was to determine whether ivacaftor potentiates mutant CFTR with gating defects caused by other CFTR gating mutations. Methods: The effects of ivacaftor on CFTR channel open probability and chloride transport were tested in electrophysiological studies using Fischer rat thyroid (FRT) cells expressing different CFTR gating mutations. Results: Ivacaftor potentiated multiple mutant CFTR forms with defects in CFTR channel gating. These included the G551D, G178R, S549N, S549R, G551S, G970R, G1244E, S1251N, S1255P and G1349D CFTR gating mutations. Conclusion: These in vitro data suggest that ivacaftor has a similar effect on all CFTR forms with gating defects and support investigation of the potential clinical benefit of ivacaftor in CF patients who have CFTR gating mutations beyond G551D. (C) 2012 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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