CPC C07K 16/3084 (2013.01) [A61K 35/17 (2013.01); A61K 38/179 (2013.01); A61K 38/1774 (2013.01); A61K 39/39558 (2013.01); C07K 14/7051 (2013.01); C07K 14/70517 (2013.01); C07K 14/70521 (2013.01); C07K 14/70578 (2013.01); C12N 15/85 (2013.01); A61K 2039/505 (2013.01); C07K 2317/21 (2013.01); C07K 2317/24 (2013.01); C07K 2317/52 (2013.01); C07K 2317/53 (2013.01); C07K 2317/565 (2013.01); C07K 2317/622 (2013.01); C07K 2317/73 (2013.01); C07K 2319/00 (2013.01); C07K 2319/03 (2013.01); C07K 2319/20 (2013.01); C07K 2319/30 (2013.01); C12N 2510/00 (2013.01)] | 2 Claims |
1. A method for treating cancer which comprises the step of administering a T cell to a subject,
wherein the T cell expresses a chimeric antigen receptor (CAR) comprising
a) a disialoganglioside (GD2)-binding domain and spacer, shown as amino acids 21 to 311 of SEQ ID NO: 29,
b) a hydrophobic alpha helical transmembrane domain, and
c) a CD28-CD3Zeta endodomain shown as SEQ ID NO: 17; and
wherein the cancer is a melanoma, medulloblastoma, soft-tissue sarcoma, osteosarcoma or small-cell lung cancer.
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