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Suppression and Replacement Gene Therapy for <i>KCNH2</i> -Mediated Arrhythmias

Sahej Bains, Wei Zhou, Steven M. Dotzler, Katherine Martinez, CS John Kim, David J. Tester, Dan Ye, Michael J. Ackerman

2022Circulation Genomic and Precision Medicine27 citationsDOIOpen Access PDF

Abstract

Background: KCNH2 -mediated arrhythmia syndromes are caused by loss-of-function (type 2 long QT syndrome [LQT2]) or gain-of-function (type 1 short QT syndrome [SQT1]) pathogenic variants in the KCNH2 -encoded K v 11.1 potassium channel, which is essential for the cardiac action potential. Methods: A dual-component “suppression-and-replacement” (SupRep) KCNH2 gene therapy was created by cloning into a single construct a custom-designed KCNH2 short hairpin RNA with ~80% knockdown (suppression) and a “short hairpin RNA-immune” KCNH2 cDNA (replacement). Induced pluripotent stem cell-derived cardiomyocytes and their CRISPR-Cas9 variant-corrected isogenic control (IC) induced pluripotent stem cell-derived cardiomyocytes were made for 2 LQT2- (G604S, N633S) and 1 SQT1- (N588K) causative variants. All variant lines were treated with KCNH2-SupRep or non-targeting control short hairpin RNA (shCT). The action potential duration (APD) at 90% repolarization (APD 90 ) was measured using FluoVolt voltage dye. Results: KCNH2-SupRep achieved variant-independent rescue of both pathologic phenotypes. For LQT2-causative variants, treatment with KCNH2-SupRep resulted in shortening of the pathologically prolonged APD 90 to near curative (IC-like) APD 90 levels (G604S IC, 471±25 ms; N633S IC, 405±55 ms) compared with treatment with shCT (G604S: SupRep-treated, 452±76 ms versus shCT-treated, 550±41 ms; P &lt;0.0001; N633S: SupRep-treated, 399±105 ms versus shCT-treated, 577±39 ms, P &lt;0.0001). Conversely, for the SQT1-causative variant, N588K, treatment with KCNH2-SupRep resulted in therapeutic prolongation of the pathologically shortened APD 90 (IC: 429±16 ms; SupRep-treated: 396±61 ms; shCT-treated: 274±12 ms). Conclusions: We provide the first proof-of-principle gene therapy for correction of both LQT2 and SQT1. KCNH2-SupRep gene therapy successfully normalized the pathologic APD 90 , thereby eliminating the pathognomonic feature of both LQT2 and SQT1.

Topics & Concepts

MedicineGene knockdownhERGLong QT syndromeInduced pluripotent stem cellRepolarizationSmall hairpin RNAInternal medicineQT intervalPotassium channelBiologyGeneElectrophysiologyGeneticsEmbryonic stem cellCardiac electrophysiology and arrhythmiasViral Infections and Immunology ResearchPluripotent Stem Cells Research
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