Low free drug concentration prevents inhibition of F508del CFTR functional expression by the potentiator VX-770 (ivacaftor).

Elizabeth Matthes, Julie Goepp, Graeme W Carlile, Yishan Luo, Kurt Dejgaard, Arnaud Billet, Renaud Robert, David Y Thomas, John W Hanrahan
Author Information
  1. Elizabeth Matthes: Department of Physiology, McGill University, Montréal, QC, Canada.
  2. Julie Goepp: Department of Physiology, McGill University, Montréal, QC, Canada.
  3. Graeme W Carlile: CF Translational Research Centre, McGill University, Montréal, QC, Canada.
  4. Yishan Luo: Department of Physiology, McGill University, Montréal, QC, Canada.
  5. Kurt Dejgaard: Department of Biochemistry, McGill University, Montréal, QC, Canada.
  6. Arnaud Billet: Department of Physiology, McGill University, Montréal, QC, Canada.
  7. Renaud Robert: Department of Physiology, McGill University, Montréal, QC, Canada.
  8. David Y Thomas: CF Translational Research Centre, McGill University, Montréal, QC, Canada.
  9. John W Hanrahan: Department of Physiology, McGill University, Montréal, QC, Canada.

Abstract

BACKGROUND AND PURPOSE: The most common cystic fibrosis (CF) mutation F508del inhibits the gating and surface expression of CFTR, a plasma membrane anion channel. Optimal pharmacotherapies will probably require both a 'potentiator' to increase channel open probability and a 'corrector' that improves folding and trafficking of the mutant protein and its stability at the cell surface. Interaction between CF drugs has been reported but remains poorly understood.
EXPERIMENTAL APPROACH: CF bronchial epithelial cells were exposed to the corrector VX-809 (lumacaftor) and potentiator VX-770 (ivacaftor) individually or in combination. Functional expression of CFTR was assayed as the forskolin-stimulated short-circuit current (Isc ) across airway epithelial monolayers expressing F508del CFTR.
KEY RESULTS: The potentiated Isc response during forskolin stimulation was increased sixfold after pretreatment with VX-809 alone and reached ~11% that measured across non-CF monolayers. VX-770 (100 nM) and genistein (50 μM) caused similar levels of potentiation, which were not additive and were abolished by the CFTR inhibitor CFTRinh -172. The unbound fraction of VX-770 in plasma was 0.13 ± 0.04%, which together with previous measurements in patients given 250 mg p.o. twice daily, suggests a peak free plasma concentration of 1.5-8.5 nM. Chronic exposure to high VX-770 concentrations (>1 μM) inhibited functional correction by VX-809 but not in the presence of physiological protein levels (20-40 mg·mL(-1) ). Chronic exposure to a low concentration of VX-770 (100 nM) together with VX-809 (1 μM) also did not reduce the forskolin-stimulated Isc , relative to cells chronically exposed to VX-809 alone, provided it was assayed acutely using the same, clinically relevant concentration of potentiator.
CONCLUSIONS AND IMPLICATIONS: Chronic exposure to clinically relevant concentrations of VX-770 did not reduce F508del CFTR function. Therapeutic benefit of VX-770 + VX-809 (Orkambi) is probably limited by the efficacy of VX-809 rather than by inhibition by VX-770.

References

  1. Lancet Respir Med. 2014 Jul;2(7):527-38 [PMID: 24973281]
  2. Clin Chim Acta. 1985 Oct 15;151(3):193-216 [PMID: 3902293]
  3. Cell. 1990 Nov 16;63(4):827-34 [PMID: 1699669]
  4. Clin Chem. 1995 Oct;41(10):1522-5 [PMID: 7586528]
  5. J Biol Chem. 1993 Oct 15;268(29):21592-8 [PMID: 7691813]
  6. Proc Natl Acad Sci U S A. 2011 Nov 15;108(46):18843-8 [PMID: 21976485]
  7. Nat Rev Drug Discov. 2010 Dec;9(12):929-39 [PMID: 21119731]
  8. Am J Respir Cell Mol Biol. 1993 May;8(5):522-9 [PMID: 7683197]
  9. Science. 1989 Sep 8;245(4922):1066-73 [PMID: 2475911]
  10. J Cyst Fibros. 2014 Jan;13(1):29-36 [PMID: 23891399]
  11. J Cyst Fibros. 2012 May;11(3):237-45 [PMID: 22293084]
  12. Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18825-30 [PMID: 19846789]
  13. Trends Pharmacol Sci. 2013 Feb;34(2):119-25 [PMID: 23380248]
  14. Br J Pharmacol. 2013 Dec;170(8):1607-51 [PMID: 24528239]
  15. Nucleic Acids Res. 2014 Jan;42(Database issue):D1098-106 [PMID: 24234439]
  16. Am J Respir Cell Mol Biol. 2006 Jul;35(1):20-8 [PMID: 16528010]
  17. Science. 1991 Jul 12;253(5016):202-5 [PMID: 1712984]
  18. Sci Transl Med. 2014 Jul 23;6(246):246ra96 [PMID: 25101886]
  19. Science. 1989 Sep 8;245(4922):1059-65 [PMID: 2772657]
  20. J Mol Recognit. 2015 Jun;28(6):339-48 [PMID: 25707701]
  21. Br J Pharmacol. 2016 Feb;173(3):459-70 [PMID: 26492939]
  22. Cell. 1991 Feb 22;64(4):681-91 [PMID: 1705179]
  23. Sci Transl Med. 2014 Jul 23;6(246):246ra97 [PMID: 25101887]
  24. Chem Biol Interact. 2005 Jan 15;151(2):53-62 [PMID: 15698577]
  25. Nature. 1991 Dec 19-26;354(6354):526-8 [PMID: 1722027]
  26. Drugs. 2013 Sep;73(14):1595-604 [PMID: 24030637]
  27. Front Pharmacol. 2014 Oct 31;5:231 [PMID: 25400580]
  28. Mol Ther. 2000 Jul;2(1):47-55 [PMID: 10899827]
  29. Cell. 1992 Feb 21;68(4):809-18 [PMID: 1371239]
  30. Methods Mol Med. 2005;107:183-206 [PMID: 15492373]
  31. Mol Pharmacol. 2008 Feb;73(2):478-89 [PMID: 17975008]
  32. J Physiol. 2005 Dec 1;569(Pt 2):601-15 [PMID: 16210354]

Grants

  1. /Canadian Institutes of Health Research

MeSH Term

Aminophenols
Aminopyridines
Benzodioxoles
Bronchi
Cell Line
Cells, Cultured
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Drug Interactions
Epithelial Cells
Humans
Mutation
Quinolones

Chemicals

Aminophenols
Aminopyridines
Benzodioxoles
Quinolones
Cystic Fibrosis Transmembrane Conductance Regulator
ivacaftor
lumacaftor

Word Cloud

Created with Highcharts 10.0.0VX-770VX-809CFTRF508delconcentrationCFexpressionplasmapotentiatorIscChronicexposureANDsurfacechannelprobablyproteinepithelialcellsexposedivacaftorassayedforskolin-stimulatedacrossmonolayersalone100 nMlevels0togetherfreeconcentrationsfunctionalreduceclinicallyrelevantinhibitionBACKGROUNDPURPOSE:commoncysticfibrosismutationinhibitsgatingmembraneanionOptimalpharmacotherapieswillrequire'potentiator'increaseopenprobability'corrector'improvesfoldingtraffickingmutantstabilitycellInteractiondrugsreportedremainspoorlyunderstoodEXPERIMENTALAPPROACH:bronchialcorrectorlumacaftorindividuallycombinationFunctionalshort-circuitcurrentairwayexpressingKEYRESULTS:potentiatedresponseforskolinstimulationincreasedsixfoldpretreatmentreached~11%measurednon-CFgenistein50 μMcausedsimilarpotentiationadditiveabolishedinhibitorCFTRinh-172unboundfraction13±04%previousmeasurementspatientsgiven250 mgpotwicedailysuggestspeak15-85 nMhigh>1 μMinhibitedcorrectionpresencephysiological20-40 mg·mL-1low1 μMalsorelativechronicallyprovidedacutelyusingCONCLUSIONSIMPLICATIONS:functionTherapeuticbenefit+OrkambilimitedefficacyratherLowdrugprevents

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