The Journal of Cardiovascular Aging · 2024 · 10 citations · 25 references
MedicineCardiologyGeneticsCardiovascular GeneticsGene TherapyGenome EditingAllele-specific EditingTherapeutic Genome EditingCrispr-cas Genome EditingCrispr-cas9 Genome EditingGene Editing TherapyGenome Editing DeliveryGuide Rna-directed EditingManagement Of Ventricular TachycardiaMutant Allele DisruptionSomatic Cell Editing
Introduction: Heterozygous autosomal-dominant single nucleotide variants in RYR2 account for 60% of cases of catecholaminergic polymorphic ventricular tachycardia (CPVT), an inherited arrhythmia disorder associated with high mortality rates. CRISPR/Cas9-mediated genome editing is a promising therapeutic approach that can permanently cure the disease by removing the mutant RYR2 allele. However, the safety and long-term efficacy of this strategy have not been established in a relevant disease model. Aim: The purpose of this study was to assess whether adeno-associated virus type-9 (AAV9)-mediated somatic genome editing could prevent ventricular arrhythmias by removal of the mutant allele in mice that are heterozygous for Ryr2 variant p.Arg176Gln (R176Q/+). Methods and Results: Guide RNA and SaCas9 were delivered using AAV9 vectors injected subcutaneously in 10-day -old mice. At 6 weeks after injection, R176Q/+ mice had a 100% reduction in ventricular arrhythmias compared to controls. When aged to 12 months, injected R176Q/+ mice maintained a 100% reduction in arrhythmia induction. Deep RNA sequencing revealed the formation of insertions/deletions at the target site with minimal off-target editing on the wild-type allele. Consequently, CRISPR/SaCas9 editing resulted in a 45% reduction of total Ryr2 mRNA and a 38% reduction in RyR2 protein. Genome editing was well tolerated based on serial echocardiography, revealing unaltered cardiac function and structure up to 12 months after AAV9 injection. Conclusion: Taken together, AAV9-mediated CRISPR/Cas9 genome editing could efficiently disrupt the mutant Ryr2 allele, preventing lethal arrhythmias while preserving normal cardiac function in the R176Q/+ mouse model of CPVT.
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Argelia Medeiros‐Domingo, Zahurul A. Bhuiyan, David J. Tester et al. · Journal of the American College of Cardiology · 2009 · 337 citations · Full text
Medicine, Cardiology, Physiology +16
Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia
Gaetano Maria De Ferrari, Veronica Dusi, Carla Spazzolini et al. · Circulation · 2015 · 291 citations · Full text