Flexible and scalable solutions for AAV viral vector production using a templated platform
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Adeno-associated virus (AAV) has become an increasingly popular viral vector for gene therapy. Currently, there are two approved AAV-based gene therapies, and the number of clinical trials is steadily increasing. As with most viral vector therapies, their production is labour intensive and expensive due to the use of adherent cell culture production processes. For process intensification, the industry has begun to utilize bioreactors. Here, we highlight our development of a suspension based AAV upstream production process to provide a more efficient and cost-effective bioprocessing solution for large scale production
- How suspension adapted cell lines for transient transfection meet AAV production needs
- The benefits of scalable solutions with simplified production processes for viral vector manufacturing
- The importance of cell line and cell culture media compliance with GMP regulations
- Robust process design, amendable to multiple transfections reagents and serotypes
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