CPC A61K 35/15 (2013.01) [A61K 31/198 (2013.01); A61K 31/202 (2013.01); A61K 31/375 (2013.01); A61K 31/59 (2013.01); A61K 35/28 (2013.01); A61K 38/193 (2013.01); A61K 38/20 (2013.01); A61K 38/27 (2013.01); A61P 35/00 (2018.01); C12N 5/0642 (2013.01); C12N 5/0647 (2013.01); G01N 33/57438 (2013.01); C12N 2500/32 (2013.01); C12N 2500/38 (2013.01); C12N 2501/02 (2013.01); C12N 2501/145 (2013.01); C12N 2501/22 (2013.01); C12N 2501/2303 (2013.01); C12N 2501/2304 (2013.01); C12N 2501/2306 (2013.01); C12N 2501/2308 (2013.01); C12N 2501/2318 (2013.01); C12N 2501/25 (2013.01); C12N 2501/26 (2013.01); C12N 2501/305 (2013.01); C12N 2501/825 (2013.01); C12N 2506/11 (2013.01); C12N 2506/45 (2013.01)] | 13 Claims |
1. A method for treating a cancer comprising:
administering to a subject in need thereof a therapeutically effective amount of a composition comprising neutrophils derived from haematopoietic stem cells obtainable by a method, said method comprising:
a. admixing granulocytes obtained from a donor with cancer cells from a cancer cell line to form an admixture;
b. incubating said admixture;
c. measuring a percent (%) of cancer cells killed in the incubated admixture;
d. obtaining haematopoietic stem cells from a sample from the donor when the granulocytes kill at least 5% of the cancer cells in the incubated admixture; and
e. differentiating the haematopoietic stem cells from the donor to obtain the composition comprising neutrophils;
wherein the donor is allogeneic with the subject.
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