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Li L et al. – The target–specific cytotoxicity for anti–CD19–BB–z mRNA–transfected NK cells was observed as early as 3 h after transfection and persisted for up to 3 days. The method described here should facilitate the clinical development of NK–based antigen–targeted immunotherapy for cancer.

Exclusive Author Commentary
L Li, 09/16/09

Concerns for safety, simplicity, scalability and cost become more and more important for both clinical study and the following commercialization of chimeric receptor technology. This translational study demonstrated the specific cytotoxic function of expanded and unstimulated resting NK cells toward specific target cells, like tumors, could be dramatically enhanced through mRNA non-viral gene modification with chimeric receptor by a GMP-compliant method, which is safe, efficient and cost effective. The method can be applied to chimeric receptors with different specificities, is demonstrated to be scalable, and should be easily translatable to clinical setting.


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