As more and more engineered cell therapy products that utilize lentiviral (LV) vectors in their manufacture reach the market, the sector’s focus is sharpening around optimizing LV downstream processing. Given the significant contribution that LV vectors make to the overall cost of goods of these cell therapy products, and the importance of maximizing quality for patient safety and regulatory CMC purposes, it is imperative to maximize downstream purification efficiency and vector recovery, and to be able to harness the available analytical toolkit to demonstrate vector quality.
Here, we convene a panel of LV downstream process experts to explore current issues in the field, and discuss how they can be overcome utilizing the available LV purification and analytics toolkit.