IP Library Granted Patent US 10,799,536
Granted Patent B2
US 10,799,536 · App. 15/837,576 · Granted Oct 13, 2020

Method of treating multiple myeloma using natural killer cells expressing a chimeric antigen receptor for CD38

Inventor: Michael Eamon Peter O'Dwyer (Galway, IE)
Assignee: ONK Therapeutics Limited
A61K35/17A61K35/15A61K38/177A61K39/0011A61P35/00C07K16/2896A61K2035/124A61K2039/505A61K2039/5156A61K2039/5158C07K2317/56C07K2317/565C07K2319/70
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Quick Facts
Patent No.
US 10,799,536
App. No.
15/837,576
Granted
Oct 13, 2020
Kind
B2
Abstract

Disclosed herein are engineered natural killer cells that have been modified to express chimeric antigen receptors (CARs). The cells optionally contain other modifications that improve tumor specific cytotoxicity and homing to tumor sites. Also contemplated are methods for using the engineered natural killer cells to treat patients with cancer.

Claims (16)

1. A method of treating multiple myeloma (MM) in a mammal, the method comprising administering to the mammal a natural killer (NK) cell modified to express a chimeric antigen receptor (CAR) for CD38,

wherein the administering kills MM cells expressing CD38,

wherein the CD38 CAR comprises

(a) a heavy chain variable region comprising SEQ ID NO: 1 or SEQ ID NO: 7, and

(b) a light chain variable region comprising SEQ ID NO: 23 or SEQ ID NO: 28.

2. The method according to claim 1 , wherein the NK cell expresses E-selectin ligand.

3. The method according to claim 1 , wherein the NK cell binds the HECA-452 antibody.

4. The method according to claim 1 , wherein the NK cell is a KHYG-1 cell.

5. The method according to claim 1 , wherein the CD38 CAR comprises one or more or all of the heavy chain CDRs in SEQ ID NO:s 29, 30 and 31.

6. The method according to claim 1 , wherein the CD38 CAR comprises one or more or all of the heavy chain CDRs in SEQ ID NO:s 32, 33 and 34.

7. The method according to claim 1 , wherein the CD38 CAR comprises one or more or all of the light chain CDRs in SEQ ID NO:s 35, 36 and 37.

8. The method according to claim 1 , wherein the CD38 CAR comprises one or more or all of the light chain CDRs in SEQ ID NO:s 38, 39 and 40.

9. The method according to claim 1 , wherein the CD38 CAR comprises one or more co-stimulatory domains selected from SEQ ID NO: 41, SEQ ID NO: 42 and SEQ ID NO: 43.

10. The method according to claim 1 , wherein the NK cell has been modified to express a TRAIL variant that has increased affinity for TRAIL death receptors, relative to wildtype TRAIL.

11. A method of treating multiple myeloma (MM) in a mammal, the method comprising administering to the mammal a natural killer (NK) cell modified to express a chimeric antigen receptor (CAR) for CD38, wherein the administration kills MM cells expressing CD38, and wherein the CD38 CAR comprises a heavy chain variable region comprising SEQ ID NO: 1 and a light chain variable region comprising SEQ ID NO: 23.

12. The method according to claim 1 , wherein the CAR has an affinity for CD38 that is at least 25% lower than the affinity of Daratumumab for CD38.

Assignments (3)
CHANGE OF NAME Recorded Jul 3, 2020
From: ONKIMMUNE LIMITED
To: ONK THERAPEUTICS LIMITED
Reel/Frame 053115/0984 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2018
From: NATIONAL UNIVERSITY OF IRELAND, GALWAY
To: ONKIMMUNE LIMITED
Reel/Frame 044911/0559 →
CONFIRMATORY ASSIGNMENT Recorded Feb 13, 2018
From: O'DWYER, MICHAEL EAMON PETER
To: NATIONAL UNIVERSITY OF IRELAND, GALWAY
Reel/Frame 045313/0551 →
Continuity (2)
Provisional Application 62432302 · Dec 9, 2016
Related Publication 20180161371A1 · Jun 14, 2018
Cited By (1)
US 12,534,536