IP Library › Granted Patent US 11,896,616
Granted Patent B2
US 11,896,616 · App. 16/497,682 · Granted Feb 13, 2024

Stimulatory cell lines for ex vivo expansion and activation of natural killer cells

Inventors: Takahiro Kamiya (Singapore, SG); Dario Campana (Singapore, SG)
Assignee: National University of Singapore
A61K35/17C07K14/5443C07K16/2809C12N5/0646C07K2317/622C12N2502/30C12N2510/04C12N2740/10043
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 11,896,616
App. No.
16/497,682
Granted
Feb 13, 2024
Kind
B2
Abstract

The present invention relates to genetically engineered cell populations derived from an immortalised/cancerous cell that do not express MHC class I molecules but that are modified to express membrane-bound IL-15, membrane-bound 4-1 BBL ligand, and at least one other membrane bound molecule, such as an interleukin or anti-CD3 antibody. The co-culture of said cells with a population of immune cells results in the activation and expansion of at least one subpopulation of immune cells. Expanded populations of NK cells derived from the co-culture of a mixed cell culture with the stimulatory cell lines may be used in methods of treating cancer or an infectious disease. In a separate embodiment, a plurality of nucleic acids for use in preparing the engineered cell population are provided.

Claims (27)

1. A genetically engineered cell population that does not express major histocompatibility complex (MHC) I molecules,

wherein said genetically engineered cell population is derived from K562 cells,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-15 (mbIL15), wherein the mbIL15 comprises the amino acid sequence of SEQ ID NO: 2,

wherein said genetically engineered cell population is modified to express membrane-bound 4-1BB ligand (mb4-1BBL) comprising the amino acid sequence of SEQ ID NO: 14,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-18 (mbIL18), wherein the mbIL18 comprises the amino acid sequence of SEQ ID NO: 8,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-12A (mbIL12A), wherein the mbIL12A comprises the amino acid sequence of SEQ ID NO: 4,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-12B (mbIL12B), wherein the mbIL12B comprises the amino acid sequence of SEQ ID NO: 6,

wherein said genetically engineered cell population does not express major histocompatibility complex (MHC) I molecules, and

wherein co-culture of said genetically engineered cell population with a population of natural killer (NK) cells results in the activation and expansion of the NK cells.

2. The genetically engineered cell population of claim 1 , wherein the genetically engineered cell population lacks expression of MHC II molecules.

3. The genetically engineered cell population of claim 1 , wherein the genetically engineered cell population is further modified to express:

membrane-bound interleukin-21 (mbIL21) comprising the sequence of SEQ ID NO: 10; or

membrane-bound interleukin-22 (IL22) comprising the sequence of SEQ ID NO: 12.

4. The genetically engineered cell population of claim 1 , wherein the cells further comprise a membrane-bound anti-CD3 antibody (mbα-CD3), an antibody fragment thereof, or an anti-CD3 scFv.

5. The genetically engineered cell population of claim 4 , wherein the mbα-CD3 is a monoclonal antibody.

6. The genetically engineered cell population of claim 5 , wherein the mbα-CD3 targets an epitope within the epsilon subunit of the CD3 receptor.

7. A genetically engineered cell population that does not express major histocompatibility complex (MHC) I molecules,

wherein said genetically engineered cell population is derived from K562 cells,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-15 (mbIL15), wherein the mbIL15 is encoded by a nucleic acid sequence that comprises SEQ ID NO: 1,

wherein said genetically engineered cell population is modified to express membrane-bound 4-1BB ligand (mb4-1BBL) comprising the amino acid sequence of SEQ ID NO: 14,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-18 (mbIL18), wherein the mbIL18 comprises the amino acid sequence of SEQ ID NO: 8,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-12A (IL12A), wherein the mbIL12A comprises the amino acid sequence of SEQ ID NO: 4,

wherein said genetically engineered cell population is modified to express membrane-bound interleukin-12B (IL12B), wherein the mbIL12B comprises the amino acid sequence of SEQ ID NO: 6,

wherein said genetically engineered cell population does not express major histocompatibility complex (MHC) I molecules, and

wherein co-culture of said genetically engineered cell population with a population of natural killer (NK) cells results in the activation and expansion of the NK cells.

8. The genetically engineered cell population of claim 7 , wherein the amino acid sequence of SEQ ID NO:14 is encoded by a nucleic acid sequence that comprises SEQ ID NO: 13.

9. The genetically engineered cell population of claim 7 , wherein the engineered cell population is further modified to express membrane-bound interleukin-21 or membrane-bound interleukin-22.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2019
From: KAMIYA, TAKAHIRO; CAMPANA, DARIO
To: NATIONAL UNIVERSITY OF SINGAPORE
Reel/Frame 051224/0586 →
Continuity (2)
Provisional Application 62477311 · Mar 27, 2017
Related Publication 20200016208A1 · Jan 16, 2020
Cited By (7)
US 12,258,381 US 12,264,335 US 12,351,617 US 12,398,187 US 12,441,787 US 12,486,514 US 12,590,148