Notch induced natural killer cell generation and therapeutic uses
A method of preparing differentiated NK cells by ex vivo expansion includes the steps of; (1) isolating a plurality of CD34 + hematopoietic cells; (2) culturing the cells in a medium, wherein the medium includes an effective amount of a notch ligand and one or more cytokines selected from the group consisting of IL-7, IL-15, SCF, Flt-3, IL-3 and IL-6; and (3) maintaining the cells in culture for a duration of time sufficient to produce NK cells.
1. A method of preparing differentiated NK cells by ex vivo expansion comprising:
isolating a plurality of CD 34+ hematopoietic cells;
culturing the cells in a medium free of stromal cells, wherein the medium includes an effective amount of a notch ligand and IL-7, IL-15, SCF, Flt-3 and IL-3, the notch ligand being immobilized on a solid substrate that facilitates interaction of the CD34+ cells and the notch ligand, wherein the solid substrate is suspended in the medium; and
maintaining the cells in culture for a duration of time sufficient to produce NK cells.
2. The method of claim 1 , the notch ligand comprising delta4 notch ligand.
3. The method of claim 1 , wherein the NK cells lack MHC class I inhibitory signals.
4. The method of claim 1 , wherein the NK cells do not express an inhibitory receptor surface protein selected from KIR and NKG2A.
5. The method of claim 1 , the solid substrate comprising a plurality of protein A beads.
6. The method according to claim 5 , wherein the protein A beads are used at a concentration of at least 0.01 μg/ml to 100 μg/ml.
7. The method of claim 1 wherein the hematopoietic cells are derived from umbilical cord blood.
8. The method of claim 1 , the medium further comprising IL-6.
9. The method of claim 1 , the predetermined time period comprising between about 2 weeks and about 6 weeks.
10. The method of claim 1 , wherein the NK cells have at least the following characteristics: CD56 bright , CD16 − , CD117 + , KIR − , CD94 low , CD11b−.