| CPC C12N 5/0636 (2013.01) [A61K 39/4611 (2023.05); A61K 39/4631 (2023.05); A61K 39/464412 (2023.05); C12N 5/0696 (2013.01); C12N 2501/115 (2013.01); C12N 2501/125 (2013.01); C12N 2501/15 (2013.01); C12N 2501/155 (2013.01); C12N 2501/165 (2013.01); C12N 2501/2302 (2013.01); C12N 2501/2303 (2013.01); C12N 2501/2307 (2013.01); C12N 2501/2315 (2013.01); C12N 2501/26 (2013.01); C12N 2501/415 (2013.01); C12N 2501/42 (2013.01); C12N 2501/51 (2013.01); C12N 2501/515 (2013.01); C12N 2501/602 (2013.01); C12N 2501/603 (2013.01); C12N 2501/604 (2013.01); C12N 2501/606 (2013.01); C12N 2501/727 (2013.01); C12N 2501/999 (2013.01); C12N 2506/11 (2013.01); C12N 2506/45 (2013.01); C12N 2510/00 (2013.01); C12N 2533/90 (2013.01)] | 18 Claims |
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1. A method comprising:
isolating at least one stem memory T cell (Tsm);
expanding the Tsm in vitro;
reprogramming at least a portion of the expanded Tsms into iPSCs; and
differentiating at least a portion of the iPSCs into T cells, wherein differentiating comprises forming embryoid bodies (EBs) from the iPSCs and culturing the iPSCs in the presence of a Wnt pathway activator and a TGFβ signaling inhibitor, wherein the differentiated T cells comprise a Tsm.
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