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In vivo base editing rescues primary hyperoxaluria type 1 in rats
Zhoutong Chen1, Dexin Zhang2, Rui Zheng3
1Department of Urology, Children's Hospital of Fudan University, Shanghai, China.
Insights
Base editing technology successfully repaired the gene defect in a rat model of Primary Hyperoxalurua type 1 (PH1), reducing oxalate production and kidney damage. This offers a promising new gene therapy for PH1.
Area of Science:
- Genetics and Genomics
- Molecular Biology
- Gene Therapy
Background:
- Primary Hyperoxalurua type 1 (PH1) is a severe genetic kidney disease causing oxalate stones and progressive kidney damage.
- Current treatments are limited, and gene repair has historically been inefficient.
- Base editors offer precise gene correction without DNA double-strand breaks.
Purpose of the Study:
- To investigate the efficacy of adenine base editor (ABE) for in vivo gene repair in PH1.
- To assess the potential of ABE-mediated correction of the AGXT gene in a PH1 rat model.
Main Methods:
- Systemic delivery of a dual adeno-associated virus encoding a split-ABE8e.
- Utilized AgxtQ84X rats, a genetic model mimicking PH1.
- Assessed gene editing efficiency, AGT expression, oxalate synthesis, and crystal deposition.
Main Results:
- Achieved 13% repair of the pathogenic allele in PH1 rats.
- Partially restored alanine-glyoxylate-aminotransferase (AGT) expression and reduced oxalate synthesis.
- Demonstrated stable editing efficiency in the liver for six months post-treatment.
Conclusions:
- In vivo base editing with ABE8e shows promise for treating PH1 by directly correcting the AGXT gene.
- This approach offers a potential personalized and precise therapeutic strategy for PH1.
- Restored AGT protein expression and alleviated disease phenotypes in the rat model.
Abstract:
Primary hyperoxaluria type 1 (PH1) is a childhood-onset autosomal recessive disease, characterized by nephrocalcinosis, multiple recurrent urinary calcium oxalate stones, and a high risk of progressive kidney damage. PH1 is caused by inherent genetic defects of the alanine glyoxylate aminotransferase (AGXT) gene. The in vivo repair of disease-causing genes was exceedingly inefficient before the invention of base editors which can efficiently introduce precisely targeted base alterations without double-strand DNA breaks. Adenine base editor (ABE) can precisely convert A·T to G·C with the assistance of specific guide RNA. Here, we demonstrated that systemic delivery of dual adeno-associated virus encoding a split-ABE8e could artificially repair 13% of the pathogenic allele in AgxtQ84X rats, a model of PH1, alleviating the disease phenotype. Specifically, ABE treatment partially restored the expression of alanine-glyoxylate-aminotransferase (AGT), reduced endogenous oxalate synthesis and alleviated calcium oxalate crystal deposition. Western blot and immunohistochemistry confirmed that ABE8e treatment restored AGT protein expression in hepatocytes. Moreover, the precise editing efficiency in the liver remained stable six months after treatment. Thus, our findings provided a prospect of in vivo base editing as a personalized and precise medicine for PH1 by directly correcting the mutant Agxt gene.
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