CPC C12N 5/0638 (2013.01) [A61K 39/12 (2013.01); A61K 39/4611 (2023.05); A61K 39/464838 (2023.05); C07K 14/025 (2013.01); C07K 14/03 (2013.01); C07K 14/11 (2013.01); C07K 14/135 (2013.01); C12N 7/00 (2013.01); A61K 2039/55527 (2013.01); A61K 2039/57 (2013.01); A61K 2039/572 (2013.01); A61K 2039/577 (2013.01); A61K 2039/70 (2013.01); C12N 2501/2302 (2013.01); C12N 2501/2304 (2013.01); C12N 2501/2307 (2013.01); C12N 2501/2315 (2013.01); C12N 2710/16134 (2013.01); C12N 2710/16234 (2013.01); Y02A 50/30 (2018.01)] | 21 Claims |
1. A method of providing a cell therapy to an individual in need thereof, comprising administering a composition to the individual, wherein the composition comprises an ex vivo expanded polyclonal population of cytotoxic human T lymphocytes (CTLs) that target two or more viral antigens from two or more different viruses, wherein the CTLs are polyclonal CD4+ and CD8+ CTLs;
wherein one or more antigens is from a first virus, and one or more antigens is from a second virus; and wherein
(a) the first virus is BK virus, and the one or more antigens are selected from LT and VP-1; and
(b) the second virus is HHV6 virus, and the one or more antigens are selected from U14, U11, U71, U54, and U90.
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