IP Library Patent Application 17375985
Patent Application
App. No. 17/375,985

CIML NK cells and Methods Therefor

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
17/375,985
Abstract

Cytokine induced memory like (CIML) NK cells with enhanced cytotoxicity are presented. Most typically, the CIML NK cells are derived from a mononuclear cell fraction of peripheral blood or cord blood. In further contemplated aspects, the CIML NK cells are expanded and induced in a contained and automated production environment that substantially reduces operational complexity and production cost.

Claims (26)

1 . A method of producing cytokine induced memory like (CIML) NK cells, comprising:

isolating from whole blood or cord blood of an individual a mixture of mononuclear cells;

contacting the mixture of the mononuclear cells with an anti-CD16 antibody and N-803 to expand NK cells in the mixture of mononuclear cells; and

contacting the expanded NK cells with a stimulatory cytokine composition having IL-12 activity, IL-15 activity, and IL-18 activity to produce CIML NK cells that have an increase in surface markers CD25 and DNAM- 1 and a decrease in surface marker CD16 relative to the expanded NK cells before the step of contacting the expanded NK cells with the stimulatory cytokine composition.

2 . The method of claim 1 wherein the CIML NK cells further have a decrease in surface marker TIGIT relative to the expanded NK cells before the step of contacting the expanded NK cells with the stimulatory cytokine composition.

3 . The method of claim 1 wherein the mixture of mononuclear cells is not further processed to enrich NK cells.

4 . The method of claim 1 wherein the anti-CD16 antibody in the step of contacting the mixture is present at a concentration of between 0.05-1.0 mcg/ml, and wherein the N-803 in the step of contacting the mixture is present at a concentration of between 0.1-1.0 nM.

5 . The method of claim 1 wherein the NK cells are expanded to a total cell number of about 0.5-5.0×10 9 cells.

6 . The method of claim 1 wherein the step of contacting the expanded NK cells with a stimulatory cytokine composition is performed in the same container as the step of expanding the NK cells.

7 . The method of claim 1 wherein the stimulatory cytokine composition includes an IL-18/IL-12-TxM fusion protein complex, a mixture of IL-12, N-803, and IL-18, or a mixture of IL-12, IL-15, and IL-18.

8 . The method of claim 1 wherein the stimulatory cytokine composition includes the mixture of IL-12, N-803, and IL-18.

9 . The method of claim 1 further comprising re-stimulating the CIML NK cells by contacting the CIML NK cells with N-803.

10 . A method of activating NK cells to form cytokine induced memory like (CIML) NK cells, comprising:

providing whole blood or cord blood-derived NK cells; and

contacting the expanded NK cells with a stimulatory cytokine composition having IL-12 activity, IL-15 activity, and IL-18 activity to thereby produce the CIML NK cells;

wherein the CIML NK cells have an increase in surface markers CD25 and DNAM- 1 and a decrease in surface marker CD16 relative to the NK cells before the step of contacting the expanded NK cells with the stimulatory cytokine composition.

11 . The method of claim 10 wherein the NK cells are autologous relative to an individual receiving a transfusion comprising the CIML NK cells.

12 . The method of claim 10 wherein the whole blood or cord blood-derived NK cells were expanded in the presence of an anti-CD16 antibody and N-803.

13 . The method of claim 10 wherein the stimulatory cytokine composition includes the mixture of IL-12, N-803, and IL-18.

14 . The method of claim 10 further have a decrease in surface marker TIGIT relative to the expanded NK cells before the step of contacting the expanded NK cells with the stimulatory cytokine composition.

15 . A composition comprising a plurality of cord blood or whole blood derived cytokine induced memory like (CIML) NK cell having CD56 bright , CD25 high , DNAM-1 high , and CD16 low surface markers.

16 . The composition of claim 15 wherein the CIML NK cells further have TIGIT low surface markers.

17 . The composition of claim 15 wherein the CIML NK cells are autologous cells relative to an individual receiving the composition.

18 . The composition of claim 15 further comprising N-803.

19 . The composition of claim 15 , wherein the CIML NK cells secrete IFN-γ.

20 . The composition of claim 15 , wherein the CIML NK cells have enhanced cytotoxicity as compared to corresponding NK cells prior to cytokine induction.

Assignments (2)
SECURITY INTEREST Recorded Jan 2, 2024
From: IMMUNITYBIO, INC.; NANTCELL, INC.; RECEPTOME, INC.; VBC HOLDINGS LLC; ALTOR BIOSCIENCE, LLC; ETUBICS CORPORATION; IGDRASOL, INC.
To: INFINITY SA LLC, AS PURCHASER AGENT
Reel/Frame 066179/0074 →
CHANGE OF NAME Recorded Aug 18, 2021
From: NANTKWEST, INC.
To: IMMUNITYBIO, INC.
Reel/Frame 057221/0990 →