IP Library Granted Patent US 11,364,265
Granted Patent B1
US 11,364,265 · App. 17/438,386 · Granted Jun 21, 2022

Recombinant erIL-15 NK cells

Inventors: Patrick Soon-Shiong (Culver City, CA); Shahrooz Rabizadeh (Agoura Hills, CA); Kayvan Niazi (Culver City, CA); Hans G. Klingemann (Culver City, CA)
Assignees: NantCell, Inc.; NantBio, Inc.; ImmunityBio, Inc.
A61K35/17A61P35/00C07K14/5443C12N5/0646
View Patent ↗
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 11,364,265
App. No.
17/438,386
Granted
Jun 21, 2022
Kind
B1
Abstract

Systems and methods are presented that provide for improved NK cell function. In preferred aspects, NK-92 cells express recombinant er/LSP-IL-15 to so render the NK-92 cells independent of exogenous cytokines and to provide extracellular immune stimulation.

Claims (20)

1. A genetically modified NK cell, comprising a recombinant nucleic acid that includes a first segment encoding erLSP-IL-15 according to SEQ ID NO:5.

2. The genetically modified NK cell of claim 1 , wherein the NK cell is an NK-92 cell.

3. The genetically modified NK cell of claim 1 , wherein the recombinant nucleic acid is a DNA.

4. The genetically modified NK cell of claim 3 , wherein the recombinant nucleic acid is a linearized plasmid.

5. The genetically modified NK cell of claim 3 , wherein the recombinant nucleic acid further comprises a second segment encoding CD16 or a high affinity CD16.

6. The genetically modified NK cell of claim 5 , wherein the recombinant nucleic acid further comprises a third segment encoding a chimeric antigen receptor.

7. The genetically modified NK cell of claim 6 , wherein the recombinant nucleic acid further comprises a fourth segment encoding a protein that interferes with checkpoint inhibition, a protein that provides immune stimulation, a protein that binds/inhibits a cytokine involved with immune suppression, and/or a IL-15 receptor alpha chain.

8. The genetically modified NK cell of claim 1 , wherein the recombinant nucleic acid comprises a promotor having a sufficient strength to drive expression of the erLSP-IL-15 in an amount sufficient to (a) render the modified NK cell independent from exogenous cytokines, and to (b) allow for stimulation/activation of other immune competent cells that are in proximity to the modified NK cell.

9. The genetically modified NK cell of claim 1 , further comprising an antibody coupled to the cell via CD 16.

10. A method of modifying an NK cell, comprising: introducing a recombinant nucleic acid into the cell, wherein the recombinant nucleic acid comprises a first segment encoding erLSP-IL-15 according to SEQ ID NO:5.

11. The method of claim 10 , wherein the NK cell is an NK-92 cell.

12. The method of claim 10 , wherein the recombinant nucleic acid is a DNA.

13. The method of claim 12 , wherein the recombinant nucleic acid is a linearized plasmid.

14. The method of claim 12 , wherein the recombinant nucleic acid further comprises a second segment encoding CD16 or a high affinity CD16.

15. The method of claim 14 , wherein the recombinant nucleic acid further comprises a third segment encoding a chimeric antigen receptor.

16. The method of claim 15 , wherein the recombinant nucleic acid further comprises a fourth segment encoding a protein that interferes with checkpoint inhibition, a protein that provides immune stimulation, a protein that binds/inhibits a cytokine involved with immune suppression, and/or a IL-15 receptor alpha chain.

17. The method of claim 10 , wherein the recombinant nucleic acid comprises a promotor having a sufficient strength to drive expression of the erLSP-IL-15 in an amount sufficient to (a) render the modified NK cell independent from exogenous cytokines, and to (b) allow for stimulation/activation of other immune competent cells that are in proximity to the modified NK cell.

18. The method of claim 10 , further comprising an antibody coupled to the cell via CD16.

19. A pharmaceutical composition comprising a pharmaceutically acceptable carrier in combination with a genetically modified NK cell according to claim 1 .

20. The pharmaceutical composition of claim 19 , comprising at least 1×10 9 cells per dosage unit.

Assignments (5)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2021
From: NIAZI, KAYVAN
To: NANTBIO, INC.
Reel/Frame 058036/0869 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2021
From: KLINGEMANN, HANS
To: NANTKWEST, INC.
Reel/Frame 058036/0935 →
CHANGE OF NAME Recorded Nov 5, 2021
From: NANTKWEST, INC.
To: IMMUNITYBIO, INC.
Reel/Frame 058040/0426 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2021
From: RABIZADEH, SHAHROOZ; SOON-SHIONG, PATRICK; NIAZI, KAYVAN; KLINGEMANN, HANS
To: NANTCELL, INC.
Reel/Frame 057947/0755 →
Continuity (1)
Provisional Application 62819256 · Mar 15, 2019
Cited By (1)
US 12,435,122