Lentiviral vectors (LVVs) are widely used as a delivery system for ex vivo cell and gene therapies. In recent years, growing interest in using LVVs for in vivo therapies has driven new demand for high-quality LVVs at scale. Transient transfection systems, the dominant method used for LVV production, have well-documented limitations in scalability and product quality. In response to these limitations, therapeutic developers have begun adopting stable LV production systems, which promise to bring LVV manufacturing in line with the gold-standard practices used for protein biologics production.
In this GEN webinar, LV expert Brianna Jayanthi, PhD, will discuss how Asimov’s LV Edge Producer and Packaging Systems are leading to higher-quality, higher-productivity cell lines to support clinical and commercial LV therapies. She will present a case study evaluating transient, semi-stable, and stable LVV production systems through a manufacturing and product quality lens and offer guidance to help determine which production system is best suited for various therapeutic use cases.