| CPC A61K 40/31 (2025.01) [A61K 40/11 (2025.01); A61K 40/42 (2025.01); A61K 40/4211 (2025.01); C12N 5/0636 (2013.01); C12N 5/10 (2013.01); A61K 2035/124 (2013.01)] | 20 Claims |
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1. A method of treating systemic lupus erythematosus (SLE) in a human subject, the method comprising intravenously administering a dose of genetically engineered CD4+ and CD8+ T cells to a human subject with SLE, wherein:
the CD4+ and CD8+ T cells of the dose are at a ratio, wherein the ratio is between at or about 5:1 and at or about 1:3;
the dose of genetically engineered CD4+ and CD8+ T cells is between at or about 5×106 to 500×106 cells; and
the CD4+ and CD8+ T cells are genetically engineered with a chimeric antigen receptor (CAR), wherein the CAR comprises an scFv that binds CD19, a transmembrane domain, and an intracellular signaling domain comprising a 4-1BB costimulatory signaling domain and a CD3zeta signaling domain.
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