| CPC C12N 5/0646 (2013.01) [A61K 31/436 (2013.01); A61K 31/506 (2013.01); A61K 31/7084 (2013.01); A61K 31/7105 (2013.01); A61K 31/713 (2013.01); A61K 39/4613 (2023.05); A61K 39/464406 (2023.05); A61K 39/464424 (2023.05); A61K 45/06 (2013.01); A61P 31/00 (2018.01); A61P 35/00 (2018.01); A61P 37/06 (2018.01); C12N 5/0636 (2013.01); G01N 33/505 (2013.01); A61K 38/2086 (2013.01); A61K 2239/38 (2023.05); A61K 2239/48 (2023.05); A61K 2239/55 (2023.05); A61K 2239/59 (2023.05); C12N 2501/06 (2013.01); C12N 2501/2312 (2013.01); C12N 2501/2318 (2013.01); C12N 2501/25 (2013.01); C12N 2501/727 (2013.01); C12N 2501/999 (2013.01); C12N 2503/02 (2013.01); Y02A 50/30 (2018.01)] | 27 Claims |
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1. A composition comprising immune cells, and at least one agent, wherein:
(a) the immune cells comprise a population of modulated immune cells that are modulated by the at least one agent;
(b) the population of modulated immune cells have improved therapeutic potential in comparison to unmodulated immune cells that are not modulated by the at least one agent;
(c) the at least one agent comprises a GSK3 Inhibitor;
(d) the immune cells are genetically modified to comprise an insertion, a deletion, or a nucleic acid replacement; and
(e) the modulated immune cells comprise NK cells.
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