Recent Advances in Adeno-Associated Virus-Mediated Gene Therapy and Vaccine Development
A special issue of Pharmaceutics (ISSN 1999-4923). This special issue belongs to the section "Gene and Cell Therapy".
Deadline for manuscript submissions: 20 September 2024 | Viewed by 49
Special Issue Editors
Interests: HBV; RNAi; siRNA; shRNA; miRNA; cccDNA
Interests: adeno-associated viral vectors; adenoviral vectors; antiviral gene therapy; antiviral vaccine development; hepatitis B virus; hepatitis B virus infection models
Special Issue Information
Dear Colleagues,
AAVs have become the key to gene therapy development in recent years. Multiple lines of evidence highlight AAVs as the safest gene therapy delivery vehicle, and several AAV-based products have been approved for clinical applications. However, there has also been evidence of toxicities in patients following AAV therapy, suggesting that AAVs are not a perfect fit for all. Because AAVs have been thought to stimulate a weaker immune response, they have been overlooked for vaccine development. However, studies illustrating the potential of AAVs as vaccines are starting to emerge. Whether the inherent long-term transgene expression of AAVs could be an advantage or limit their application in vaccine development is still being explored. This Special Issue aims to collate recent findings with regard to the efficacy, safety, and feasibility of using AAVs as gene therapeutics or vaccines against a variety of communicable and non-communicable diseases.
Prof. Dr. Patrick Arbuthnot
Dr. Betty Maepa
Guest Editors
Manuscript Submission Information
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Keywords
- AAV
- gene therapy
- vaccines
- infectious diseases
- communicable diseases
- genetic disorders
- non-communicable diseases
