CPC C12N 5/0636 (2013.01) [A61K 35/16 (2013.01)] | 17 Claims |
1. A leukocyte preparation comprising:
leukocytes;
erythrocytes; and
thrombocytes;
wherein the leukocyte preparation is produced according to a method comprising:
obtaining a leukocyte fraction from whole blood;
sedimenting the leukocyte fraction until a dividing line is formed between sedimented erythrocytes and a leukocyte supernatant, removing the leukocyte supernatant from the sediment, wherein the leukocyte supernatant is collected or remains in a leukocyte container;
sedimenting the leukocytes in the leukocyte container, wherein a low-leukocyte supernatant is formed, and removing the low-leukocyte supernatant from the leukocyte container;
washing the sediment in the leukocyte container with a saline solution, wherein the sedimented cells are resuspended in the saline solution, the solution is sedimented and a resulting supernatant is removed;
resuspending the sediment in the leukocyte container in a storage solution; and
storing the solution from the resuspending in a gas-permeable bag at a temperature between 20° C. and 25° C. for at least 48 hours;
wherein the method modifies the leukocyte preparation to create a leukocyte preparation that is storable at a temperature between 2° C. and 38° C. for a period of 48 hours to 168 hours without substantial loss of function and respiratory burst and phagocytosis are more than 90 percent of a fresh version of the leukocyte preparation.
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