| CPC C12N 5/0639 (2013.01) [A61K 31/475 (2013.01); A61K 31/519 (2013.01); A61K 31/573 (2013.01); A61K 31/675 (2013.01); A61K 31/704 (2013.01); A61K 38/177 (2013.01); A61K 38/50 (2013.01); A61K 40/11 (2025.01); A61K 40/4211 (2025.01); A61K 40/4221 (2025.01); A61K 40/4224 (2025.01); A61K 40/4234 (2025.01); A61K 45/06 (2013.01); A61N 5/10 (2013.01); A61P 35/00 (2018.01); C12N 5/0636 (2013.01); C12Y 305/01001 (2013.01); A61K 2035/124 (2013.01); A61K 2239/31 (2023.05); A61K 2239/38 (2023.05); A61K 2239/48 (2023.05); C12N 2501/2302 (2013.01); C12N 2501/2321 (2013.01); C12N 2510/00 (2013.01)] | 15 Claims |
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1. A composition for treating a canine or a feline animal in need thereof, wherein the composition comprises a modified CD20 antigen specific cell primed by a cell presenting a recombinant CD20 or an antigenic fragment thereof, wherein the composition comprises at least 1.55×105 modified CD20 antigen specific cells/kg recipient weight, wherein the modified CD20 antigen specific cell is a propagated T cell.
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