Khanal Supreet, Baer Alan, Bhattarai Nirjal
Tumor Vaccine and Biotechnology Branch, Office of Cellular Therapy and Human Tissues, Office of Therapeutic Products, Center for Biologics Evaluation and Research, U.S. FDA, Silver Spring, Maryland, USA.
Tumor Vaccine and Biotechnology Branch, Office of Cellular Therapy and Human Tissues, Office of Therapeutic Products, Center for Biologics Evaluation and Research, U.S. FDA, Silver Spring, Maryland, USA.
Cytotherapy. 2025 Aug;27(8):1013-1022. doi: 10.1016/j.jcyt.2025.05.008. Epub 2025 May 22.
Ex vivo manufacturing of CAR-NK cells is a complex, multistep process involving NK cell activation, genetic modification, and cellular expansion. Currently, tumor cell-derived feeder cells (e.g., K562) are commonly used to manufacture CAR-NK cells. However, the feeder cell-based (FCB) method presents several risks to the CAR-NK product, including contamination, residual impurities, immunogenicity, and lot-to-lot variability. Additionally, establishing and maintaining feeder cells increases costs, complicates scaling up production, and requires rigorous quality control to ensure safety. In contrast, the feeder cell-free (FCF) method can mitigate these risks.
We used phorbol ester (PMA) and calcium ionophore (ionomycin) to develop a novel FCF method to manufacture CAR-NK cells and compared their critical quality attributes (CQAs) with those produced using a traditional FCB method.
In small-scale production, most CQAs were comparable between the two methods, except for CAR expression, which was lower in the FCF method. However, in large-scale production, CAR expression was comparable between the two methods, and the FCF method significantly improved CAR-NK potency while reducing CAR-NK-mediated myeloid cell activation.
Our data suggest that the FCF method provides a robust and scalable alternative for producing safer and high-quality CAR-NK cells.