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Scalable process development of NK and CAR-NK expansion in a closed bioreactor. | LitMetric

Scalable process development of NK and CAR-NK expansion in a closed bioreactor.

Front Immunol

Department of Pathology, Immunology and Laboratory Medicine, New Jersey Medical School, Rutgers-The State University of New Jersey, Newark, NJ, United States.

Published: August 2024

AI Article Synopsis

  • Large-scale production of functional natural killer (NK) and CAR-NK cells is currently a major challenge in NK-based cancer immunotherapy.
  • A new method using G-Rex 100M bioreactors was developed, which enhances oxygen delivery and allows for the effective expansion of these cells in larger volumes for therapy.
  • The NK and CAR-NK cells produced using this method maintained their ability to target and kill cancer cells and showed good viability after freezing, indicating potential for future clinical use as accessible "off-the-shelf" therapies.

Article Abstract

Production of large amounts of functional NK and CAR-NK cells represents one of the bottlenecks for NK-based immunotherapy. In this study, we developed a large-scale, reliable, and practicable NK and CAR-NK production using G-Rex 100M bioreactors, which depend on a gas-permeable membrane technology. This system holds large volumes of medium with enhanced oxygen delivery, creating conditions conducive to large-scale PBNK and CAR-NK expansions for cancer therapy. Both peripheral blood NK cells (PBNKs) and CAR-NKs expanded in these bioreactors retained similar immunophenotypes and exhibited comparable cytotoxicity towards hepatocellular carcinoma (HCC) cells akin to that of NK and CAR-NK cells expanded in G-Rex 6 well bioreactors. Importantly, cryopreservation minimally affected the cytotoxicity of NK cells expanded using the G-Rex 100M bioreactors, establishing a robust platform for scaled-up NK and CAR-NK cell production. This method is promising for the development of "off-the-shelf" NK cells, supporting the future clinical implementation of NK cell immunotherapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11303211PMC
http://dx.doi.org/10.3389/fimmu.2024.1412378DOI Listing

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