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Author Spotlight: Efficient Adeno-Associated Virus Isolation for Pre-Clinical Applications
Published on: February 9, 2024
An Overview of Nonclinical and Clinical Liver Toxicity Associated With AAV Gene Therapy
1Pfizer Inc., Cambridge, Massachusetts, USA.
Abstract:
This article reviews the presentation given at the 2023 annual meeting of the Society of Toxicologic Pathology (STP) on liver toxicity observed with adeno-associated viral vector (AAV) gene therapy. After decades as a therapeutic modality largely confined to the academic research environment, gene therapy has emerged in recent years as a rapidly expanding therapeutic approach in the biopharmaceutical industry with AAV as the most commonly used viral vector for gene delivery. This interest in the field of gene therapy by industry has been enhanced by the recent success of approved therapies for curing genetic diseases such as ZOLGENSMA for spinal muscular atrophy and LUXTURNA for Leber congenital amaurosis. However, recently reported clinical and nonclinical toxicities highlight the challenges in safely developing AAV gene therapies that require high dose systemic administration. The presentation reviewed general attributes of AAV as a gene therapy vector, clinical and nonclinical liver toxicity associated with AAV gene therapy and the potential for a multimodal immune suppression strategy that may mitigate toxicities.
Insights
Adeno-associated viral vector (AAV) gene therapy shows promise but can cause liver toxicity, especially at high doses. Multimodal immune suppression may help mitigate these risks in future treatments.
Area of Science:
- Toxicology
- Gene Therapy
- Biopharmaceutical Industry
Background:
- Gene therapy, utilizing adeno-associated viral vectors (AAV), is a rapidly expanding therapeutic approach in the biopharmaceutical industry.
- Approved therapies like ZOLGENSMA and LUXTURNA highlight the clinical success of AAV-based gene therapy for genetic diseases.
- However, challenges remain in safely developing AAV gene therapies, particularly concerning toxicities associated with high-dose systemic administration.
Conclusions:
- Safe development of adeno-associated viral vector (AAV) gene therapies requires careful consideration of liver toxicity.
- High-dose systemic administration necessitates strategies to manage potential adverse effects.
- Multimodal immune suppression is a potential approach to mitigate AAV-associated toxicities.
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