IP Library Granted Patent US 11,059,879
Granted Patent B2
US 11,059,879 · App. 15/771,128 · Granted Jul 13, 2021

Chimeric antigen receptor molecules and uses thereof

Inventors: Radhika Thokala (Houston, TX); Laurence J.N. Cooper (Houston, TX); Simon Olivares (Houston, TX)
Assignee: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
C07K14/70517A61K39/00A61K39/39558A61K39/44A61P35/00A61P35/02C07K14/7051C07K14/70521C07K16/2866A61K38/00A61K2039/507A61K2039/5158C07K2317/56C07K2317/565C07K2319/02C07K2319/03C07K2319/30
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Quick Facts
Patent No.
US 11,059,879
App. No.
15/771,128
Granted
Jul 13, 2021
Kind
B2
Abstract

Chimeric antigen receptor (CAR) polypeptides are provided comprising an antigen binding domain; a hinge domain; a transmembrane domain and an intracellular signaling domain, wherein the CAR polypeptide binds to a target antigen and wherein the antigen binding domain comprises HCDR sequences from a first antibody that binds to the target antigen and LCDR sequences from a second antibody that binds to the target antigen. In certain aspects, the target antigen is CD123.

Claims (21)

1. A chimeric antigen receptor (CAR) polypeptide comprising, from N- to C-terminus, an antigen binding domain; a hinge domain; a transmembrane domain and an intracellular signaling domain, wherein the CAR polypeptide binds to a target antigen and wherein the antigen binding domain comprises HCDR sequences from a first antibody that binds to the target antigen and LCDR sequences from a second antibody that binds to the target antigen, wherein the target antigen is CD123, wherein the antigen binding domain comprises:

(i) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 33, a VHCDR2 amino acid sequence comprising SEQ ID NO: 34, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 35; and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 24, a VLCDR2 amino acid sequence comprising SEQ ID NO: 25, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 26;

(ii) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 27, a VHCDR2 amino acid sequence comprising SEQ ID NO: 28, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 29; and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 24, a VLCDR2 amino acid sequence comprising SEQ ID NO: 25, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 26;

(iii) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising

SEQ ID NO: 39, a VHCDR2 amino acid sequence comprising SEQ ID NO: 40, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 41; and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 36, a VLCDR2 amino acid sequence comprising SEQ ID NO: 37, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 38; or

(iv) a heavy chain variable region (VH) having a VHCDR1 amino acid sequence comprising SEQ ID NO: 21, a VHCDR2 amino acid sequence comprising SEQ ID NO: 22, and a VHCDR3 amino acid sequence comprising SEQ ID NO: 23; and a light chain variable region (VL) having a VLCDR1 amino acid sequence comprising SEQ ID NO: 30, a VLCDR2 amino acid sequence comprising SEQ ID NO: 31, and a VLCDR3 amino acid sequence comprising SEQ ID NO: 32.

2. The polypeptide of claim 1 , wherein the hinge domain is a CD8a hinge having a sequence comprising KPTTTPAPRPPTPAPTIASQPLSLRPEACRPAAGGAVHTRGLD (SEQ ID NO: 12) or an IgG4 hinge having a sequence comprising ESKYGPPCPPCPAPEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEVQFNWY VDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTIS KAKGQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPP VLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLGKM (SEQ ID NO: 13).

3. The polypeptide of claim 1 , wherein the transmembrane domain is a CD8a transmembrane domain having a sequence comprising FACDIYIWAPLAGTCGVLLLSLVITLYCNHRN (SEQ ID NO: 14) or a CD28 transmembrane domain having a sequence comprising FWVLVVVGGVLACYSLLVTVAFIIFWV (SEQ ID NO: 15).

4. The polypeptide of claim 1 , wherein the intracellular signaling domain comprises a CD3z intracellular signaling domain having a sequence comprising RVKFSRSADAPAYQQGQNQLYNELNLGRREEYDVLDKRRGRDPEMGGKPRRKNPQEG LYNELQKDKMAEAYSEIGMKGERRRGKGHDGLYQGLSTATKDTYDALHMQALPPR (SEQ ID NO: 16).

5. A nucleic acid molecule encoding a CAR polypeptide in accordance with claim 1 .

6. The nucleic acid molecule of claim 5 , wherein the sequence encoding the CAR polypeptide is operatively linked to expression control sequences.

7. An isolated immune effector cell comprising a CAR polypeptide in accordance with claim 1 .

8. The cell of claim 7 , wherein the nucleic acid is integrated into the genome of the cell.

9. The cell of claim 7 , wherein the cell is a T-cell.

10. The cell of claim 7 , wherein the cell is a human cell.

11. A pharmaceutical composition comprising a population of cells in accordance with claim 10 in a pharmaceutically acceptable carrier.

12. A method of treating a subject comprising administering an anti-tumor effective amount of chimeric antigen receptor (CAR) T-cells that expresses a CAR polypeptide according to claim 1 .

13. The method of claim 12 , wherein the CAR-T cells are allogeneic cells.

14. The method of claim 12 , wherein the CAR-T cells are autologous cells.

15. The method of claim 12 , wherein the CAR-T cells are HLA matched to the subject.

16. The method of claim 12 , wherein the subject has a cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2019
From: THOKALA, RADHIKA; COOPER, LAURENCE JN; OLIVARES, SIMON
To: BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 049572/0250 →
Continuity (2)
Provisional Application 62246931 · Oct 27, 2015
Related Publication 20190055299A1 · Feb 21, 2019