IP Library Granted Patent US 11,000,550
Granted Patent B2
US 11,000,550 · App. 16/903,882 · Granted May 11, 2021

Genetically modified NK-92 cells and monoclonal antibodies for the treatment of cancer

Inventors: Tien Lee (San Diego, CA); Hans G. Klingemann (San Diego, CA); Barry J. Simon (San Diego, CA); Laurent Boissel (San Diego, CA)
Assignee: NANTKWEST, INC.
A61K35/17A61K39/39558C07K16/2803C07K16/2827C07K16/2887C07K16/32C12N5/0646A61K2039/5156A61K2039/572A61K2300/00C07K2317/24C07K2317/732C12N2501/2302C12N2501/48C12N2501/599C12N2501/727C12N2510/00
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Quick Facts
Patent No.
US 11,000,550
App. No.
16/903,882
Granted
May 11, 2021
Kind
B2
Abstract

This invention is directed to treatment of a subject having or suspected of having a cancer comprising administering to the subject a monoclonal antibody and NK-92 expressing Fc receptor.

Claims (9)

1. A composition comprising a plurality of engineered NK-92 cells from an engineered NK-92 cell line, wherein the engineered NK-92 cell line is genetically modified with a bicistronic nucleic acid construct that comprises a polynucleotide that encodes a CD16 polypeptide having a valine at position 158 of the mature form of the CD16 polypeptide, and a polynucleotide that encodes an interleukin-2 (IL-2) polypeptide targeted to the endoplasmic reticulum (ER), and wherein the engineered NK-92 cell line exhibits enhanced ADCC activity in combination with a monoclonal antibody.

2. The composition of claim 1 , further comprising an antibody.

3. The composition of claim 2 , wherein the CD16 polypeptide comprises an amino acid sequence having at least 90% identity to SEQ ID NO:2.

4. The composition of claim 2 , wherein the CD16 polypeptide comprises the amino acid sequence of SEQ ID NO:2.

5. The composition of claim 2 , wherein the engineered NK-92 cell line is further modified to express a suicide gene.

6. The composition of claim 2 , formulated for administration to a human subject that has cancer.

7. The composition of claim 6 , wherein the human subject has non-small cell lung cancer, multiple myeloma, leukemia, non-Hodgkin's lymphoma, metastatic breast cancer or gastric carcinoma.

8. The composition of claim 2 , wherein the antibody is a monoclonal antibody that induces ADCC.

9. The composition of claim 8 , wherein the monoclonal antibody is alemtuzumab, rituximab, trastuzumab, avelumab, daratumumab or elotuzumab.

Assignments (4)
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 Oct 23, 2023
From: CAMPBELL, KERRY
To: INSTITUTE FOR CANCER RESEARCH D/B/A THE RESEARCH INSTITUTE OF FOX CHASE CANCER CENTER
Reel/Frame 065304/0975 →
CHANGE OF NAME Recorded Aug 2, 2021
From: NANTKWEST, INC.
To: IMMUNITYBIO, INC.
Reel/Frame 057059/0802 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2020
From: LEE, TIEN; KLINGEMANN, HANS G.; SIMON, BARRY J.; BOISSEL, LAURENT
To: NANTKWEST, INC.
Reel/Frame 053088/0467 →
Cited By (2)
US 12,384,852 US 12,681,020