| CPC A61K 38/2013 (2013.01) [A61K 31/663 (2013.01); A61K 31/675 (2013.01); A61K 40/11 (2025.01); A61K 40/31 (2025.01); A61K 40/32 (2025.01); A61K 40/428 (2025.01); C07K 14/5443 (2013.01); C07K 14/55 (2013.01); C12N 5/0018 (2013.01); C12N 5/0636 (2013.01); C12N 5/0638 (2013.01); C12N 15/62 (2013.01); C12N 15/8509 (2013.01); A61K 2035/122 (2013.01); A61K 2035/124 (2013.01); A61K 40/50 (2025.01); C07K 16/2809 (2013.01); C12N 2501/155 (2013.01); C12N 2501/2302 (2013.01); C12N 2501/2315 (2013.01); C12N 2501/515 (2013.01); C12N 2501/998 (2013.01); C12N 2740/10043 (2013.01)] | 19 Claims |
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1. A method of preparing and administering engineered γδ T cells for cancer immunotherapy comprising:
obtaining γδ T cells,
activating the obtained γδ T cells in the presence of an aminobisphosphonate, interleukin 2 (IL-2), and interleukin 15 (IL-15),
transducing the activated γδ T cells,
expanding the transduced γδ T cells in the absence of an aminobisphosphonate and in the presence of IL-2 and IL-15 to produce the engineered γδ T cells,
wherein the fold-expansion of the engineered γδ T cells is about 10,000-fold to about 35,000-fold, and
administering at least 105 of the engineered γδ T-cells to a patient who has cancer.
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