IP Library Granted Patent US 11,970,525
Granted Patent B2
US 11,970,525 · App. 17/078,903 · Granted Apr 30, 2024

Treatment of cancer using GFR alpha-4 chimeric antigen receptor

Inventors: Donald L. Siegel (Lansdale, PA); Michael C. Milone (Cherry Hill, NJ); Vijay Bhoj (Philadelphia, PA); Christoph Rader (Jupiter, FL)
Assignees: The Trustees of the University of Pennsylvania; Novartis AG; The Scripps Research Institute
C07K14/7051C07K14/70517C07K14/70578C07K14/71C07K16/2863C07K16/30A61K38/00A61K2039/505A61K2039/5156C07K2317/24C07K2317/33C07K2317/55C07K2317/622C07K2317/73C07K2319/00C07K2319/03C07K2319/30C07K2319/50C07K2319/70
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Quick Facts
Patent No.
US 11,970,525
App. No.
17/078,903
Granted
Apr 30, 2024
Kind
B2
Abstract

The present invention relates to compositions and methods for treating diseases, disorders or conditions associated with the expression of the Glycosyl-phosphatidylinositol (GPI)-linked GDNF family α-receptor 4 (GFRα4).

Claims (46)

1. A chimeric antigen receptor (CAR) polypeptide comprising an antigen binding domain, a transmembrane domain, and an intracellular signaling domain, wherein the antigen binding domain binds to isoform a or isoform b of human Glycosyl-phosphatidylinositol (GPI)-linked GDNF family α-receptor 4 (GFRα4) cell-surface receptor and comprises:

(a) (i) a heavy chain variable region comprising a heavy chain complementary determining region 1 (HC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 63, a heavy chain complementary determining region 2 (HC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 65, and a heavy chain complementary determining region 3 (HC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 67; and

(ii) a light chain complementary determining region 1 (LC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 71, a light chain complementary determining region 2 (LC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 73, and a light chain complementary determining region 3 (LC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 75; or

(b) (i) a heavy chain variable region comprising a heavy chain complementary determining region 1 (HC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 43, a heavy chain complementary determining region 2 (HC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 45, and a heavy chain complementary determining region 3 (HC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 47; and

(ii) a light chain complementary determining region 1 (LC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 51, a light chain complementary determining region 2 (LC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 53, and a light chain complementary determining region 3 (LC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 55.

2. The CAR polypeptide of claim 1 , wherein the antigen binding domain is an antibody or an antigen-binding fragment thereof.

3. The CAR polypeptide of claim 2 , wherein the antigen-binding fragment is a scFv.

4. The CAR polypeptide of claim 2 , wherein the antibody or antigen-binding fragment is a human antibody or a fragment thereof.

5. The CAR polypeptide of claim 1 , wherein the CAR comprises:

a light chain variable region comprising an amino acid sequence having at least one, two or three modifications but not more than 20 or 10 modifications of the amino acid sequence set forth in SEQ ID NO: 69 or SEQ ID NO: 49; or

a light chain variable region comprising an amino acid sequence with about 95% up to about 99% identity to the amino acid sequence set forth in SEQ ID NO: 69 or SEQ ID NO: 49.

6. The CAR polypeptide of claim 1 , wherein the CAR comprises:

a heavy chain variable region comprising an amino acid sequence having at least one, two or three modifications but not more than 20 or 10 modifications of the amino acid sequence set forth in SEQ ID NO: 61 or SEQ ID NO: 41: or

a heavy chain variable region comprising an amino acid sequence with about 95 up to about 99% identity to the amino acid sequence set forth in SEQ ID NO: 61 or SEQ ID NO: 41.

7. The CAR polypeptide of claim 1 , wherein the CAR comprises

(a) the amino acid sequences set forth in SEQ ID NO: 61 and SEQ ID NO: 69; or

(b) the amino acid sequences set forth in SEQ ID NO: 41 and SEQ ID NO: 49.

8. The CAR polypeptide of claim 1 , wherein the antigen binding domain comprises:

(a) the amino acid sequence selected from SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 78, or SEQ ID NO: 79;

(b) an amino acid sequence having at least one, two or three modifications but not more than 30, 20, or 10 modifications of SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 78, or SEQ ID NO: 79; or

(c) an amino acid sequence with about 95 up to about 99% identity to SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 78, or SEQ ID NO: 79.

9. The CAR polypeptide of claim 1 , wherein the transmembrane domain comprises a transmembrane domain from a protein selected from the group consisting of the alpha, beta or zeta chain of the T-cell receptor, CD28, CD3 epsilon, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137 and CD154.

10. The CAR polypeptide of claim 1 , wherein the transmembrane domain comprises:

(a) the amino acid sequence of SEQ ID NO: 6;

(b) an amino acid sequence comprising at least one, two or three modifications but not more than 5 modifications of the amino acid sequence of SEQ ID NO: 6; or

(c) a sequence with about 95 up to about 99% identity to the amino acid sequence of SEQ ID NO: 6.

11. The CAR polypeptide of claim 1 , wherein the antigen binding domain is connected to the transmembrane domain by a hinge region.

12. The CAR polypeptide of claim 11 , wherein the hinge region comprises the amino acid sequence of SEQ ID NO: 2, or a sequence with about 95 up to about 99% identity to SEQ ID NO: 2.

13. The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a functional signaling domain from a protein selected from the group consisting of an MHC class I molecule, a TNF receptor protein, an immunoglobulin-like proteins, a cytokine receptor, an integrin, a signaling lymphocytic activation molecule (SLAM protein), an activating NK cell receptor, BTLA, a Toll ligand receptor, OX40, CD2, CD7, CD27, CD28, CD30, CD40, CDS, ICAM-1, LFA-1 (CD11a/CD18), 4-1BB (CD137), B7-H3, CDS, ICAM-1, ICOS (CD278), GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, LFA-1, ITGB7, NKG2D, NKG2C, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRTAM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, and a ligand that specifically binds with CD83.

14. The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises the amino acid sequence of SEQ ID NO: 7, or an amino acid sequence having at least one, two or three modifications but not more than 10 or 5 modifications of the amino acid sequence of SEQ ID NO: 7, or a sequence with about 95 up to about 99% identity to the amino acid sequence of SEQ ID NO: 7.

15. The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a functional signaling domain of 4-1BB and/or a functional signaling domain of CD3 zeta.

16. The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises:

(a) the amino acid sequence of SEQ ID NO: 7 and/or the sequence of SEQ ID NO: 9 or SEQ ID NO: 10; or

(b) an amino acid sequence having at least 1, one, two or three modifications but not more than 10 or 5 modifications of the amino acid sequence of SEQ ID NO: 7 and/or the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10; or

(c) a sequence with about 95 up to about 99% identity to the amino acid sequence of SEQ ID NO: 7 and/or the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10.

17. The CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises the sequence of SEQ ID NO: 7 and the sequence of SEQ ID NO: 9 or SEQ ID NO: 10, wherein the sequences comprising the intracellular signaling domain are expressed as a single polypeptide chain.

18. The CAR polypeptide of claim 1 , further comprising a leader sequence comprising the amino acid sequence of SEQ ID NO: 1.

19. The CAR polypeptide of claim 1 , wherein the CAR comprises:

(a) the amino acid sequence of any of SEQ ID NOs: 85, 86, 90, 92, 94, 96, 98, 100, 102, or 104;

(b) an amino acid sequence having at least one, two or three modifications but not more than 30, 20 or 10 modifications to any of SEQ ID NOs: 85, 86, 90, 92, 94, 96, 98, 100, 102, or 104; or

(c) an amino acid sequence with about 95 up to about 99% identity to any of SEQ ID NOs: 85, 86, 90, 92, 94, 96, 98, 100, 102, or 104.

20. A chimeric antigen receptor (CAR) polypeptide, wherein the CAR comprises an antigen binding domain, a transmembrane domain, and an intracellular signaling domain, and wherein the antigen binding domain binds to both isoforms a and b of human Glycosyl-phosphatidylinositol (GPI)-linked GDNF family α-receptor 4 (GFRα4) cell-surface receptor and comprises:

(a) (i) a heavy chain variable region comprising a heavy chain complementary determining region 1 (HC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 63, a heavy chain complementary determining region 2 (HC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 65, and a heavy chain complementary determining region 3 (HC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 67; and

(ii) a light chain complementary determining region 1 (LC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 71, a light chain complementary determining region 2 (LC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 73, and a light chain complementary determining region 3 (LC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 75; or

(b) (i) a heavy chain variable region comprising a heavy chain complementary determining region 1 (HC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 43, a heavy chain complementary determining region 2 (HC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 45, and a heavy chain complementary determining region 3 (HC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 47; and

(ii) a light chain complementary determining region 1 (LC CDR1) comprising the amino acid sequence set forth in SEQ ID NO: 51, a light chain complementary determining region 2 (LC CDR2) comprising the amino acid sequence set forth in SEQ ID NO: 53, and a light chain complementary determining region 3 (LC CDR3) comprising the amino acid sequence set forth in SEQ ID NO: 55.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2026
From: UNIVERSITY OF FLORIDA BOARD OF TRUSTEES
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED
Reel/Frame 075098/0564 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2024
From: THE SCRIPPS RESEARCH INSTITUTE
To: UNIVERSITY OF FLORIDA BOARD OF TRUSTEES
Reel/Frame 067978/0681 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2024
From: SIEGEL, DONALD L.; MILONE, MICHAEL C.; BHOJ, VIJAY
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 066963/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2024
From: RADER, CHRISTOPH
To: THE SCRIPPS RESEARCH INSTITUTE
Reel/Frame 066963/0744 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2024
From: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA; NOVARTIS AG
Reel/Frame 066964/0119 →
Continuity (3)
Division 15503971
Provisional Application 62037383 · Aug 14, 2014
Related Publication 20210079059A1 · Mar 18, 2021