IP Library Granted Patent US 8,859,736
Granted Patent B2
US 8,859,736 · App. 13/031,010 · Granted Oct 14, 2014

Monoclonal antibodies that inhibit the wnt signaling pathway and methods of production and use thereof

Inventors: Jian-Xing Ma (Edmond, OK); Kyungwon Lee (Oklahoma City, OK); Ying Chen (Oklahoma City, OK)
Assignee: The Board of Regents of the University of Oklahoma
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Quick Facts
Patent No.
US 8,859,736
App. No.
13/031,010
Granted
Oct 14, 2014
Kind
B2
Abstract

Monoclonal antibodies against LRP6 and that block the Wnt signaling pathway are disclosed. Methods of production and use thereof are also disclosed.

Claims (51)

1. An isolated monoclonal antibody or antigen binding fragment thereof comprising:

a light chain variable region CDR1 having the amino acid sequence of SEQ ID NO: 15;

a light chain variable region CDR2 having the amino acid sequence of SEQ ID NO: 17;

a light chain variable region CDR3 having the amino acid sequence of SEQ ID NO: 19;

a heavy chain variable region CDR1 having the amino acid sequence of SEQ ID NO: 9;

a heavy chain variable region CDR2 having the amino acid sequence of SEQ ID NO: 11;

a heavy chain variable region CDR3 having the amino acid sequence of SEQ ID NO: 13; and

wherein the monoclonal antibody or antigen binding fragment thereof specifically binds to an epitope within the LRP6 extracellular domain, wherein the LRP6 extracellular domain has the amino acid sequence of SEQ ID NO: 2.

2. The isolated monoclonal antibody or antigen binding fragment thereof of claim 1 , wherein the monoclonal antibody or antigen binding fragment thereof has:

a heavy chain variable region amino acid sequence that is at least 90% identical to SEQ ID NO: 5, and wherein the CDR1, CDR2, and CDR3 thereof are 100% identical to the amino acid sequences of SEQ ID NOS:9, 11, and 13, respectively; and

a light chain variable region amino acid sequence that is at least 90% identical to SEQ ID NO: 7, and wherein the CDR1, CDR2, and CDR3 thereof are 100% identical to the amino acid sequences of SEQ ID NOS:15, 17, and 19, respectively.

3. The isolated monoclonal antibody or antigen binding fragment thereof of claim 1 , wherein the monoclonal antibody or antigen binding fragment thereof is selected from the group consisting of a full length immunoglobulin molecule, an scFv, a Fab fragment, an Fab′ fragment, an F(ab′)2, an Fv, a disulfide linked Fv, and combinations thereof.

4. The isolated monoclonal antibody or antigen binding fragment thereof of claim 1 , wherein the monoclonal antibody or antigen binding fragment thereof is humanized.

5. The isolated monoclonal antibody or antigen binding fragment thereof of claim 1 , wherein the monoclonal antibody or antigen binding fragment thereof binds to the LRP6 extracellular domain with a dissociation constant of less than or equal to about 10 −7 M.

6. The isolated monoclonal antibody or antigen binding fragment thereof of claim 1 , wherein the monoclonal antibody or antigen binding fragment thereof binds to the same epitope as the antibody produced by the hybridoma having ATCC Designation No. PTA-10663.

7. The isolated monoclonal antibody or antigen binding fragment thereof of claim 1 , wherein the monoclonal antibody or antigen binding fragment thereof inhibits the binding of both Wnt1 and Wnt3a to LRP6.

8. A pharmaceutical composition comprising the monoclonal antibody or antigen binding fragment thereof of claim 1 and a pharmaceutically acceptable carrier.

9. The composition of claim 8 , further comprising a second agent that has a synergistic effect with the monoclonal antibody or antigen binding fragment thereof.

10. The composition of claim 9 , wherein the second agent is an anti-angiogenic agent.

11. The composition of claim 9 , wherein the second agent is an anti-VEGF reagent.

12. The hybridoma having ATCC Designation No. PTA-10663.

13. An isolated monoclonal antibody produced by the cell of claim 12 .

14. An isolated monoclonal antibody or antigen binding fragment thereof, wherein the monoclonal antibody or antigen binding fragment thereof specifically binds to the LRP6 extracellular domain having the amino acid sequence of SEQ ID NO: 2, the isolated monoclonal antibody or antigen binding fragment thereof comprising a heavy chain variable region and a light chain variable region, wherein the heavy chain has the amino acid sequence of SEQ ID NO:5 and/or a light chain variable region having the amino acid sequence of SEQ ID NO:7.

15. A method of producing a monoclonal antibody or antigen binding fragment thereof, comprising the step of:

culturing a cell that produces a monoclonal antibody or antigen binding fragment thereof under conditions that permit production of the monoclonal antibody or antigen binding fragment thereof, the monoclonal antibody or antigen binding fragment thereof comprising:

a heavy chain variable region CDR1 having the amino acid sequence of SEQ ID NO: 9, a heavy chain variable region CDR2 having the amino acid sequence of SEQ ID NO: 11, a heavy chain variable region CDR3 having the amino acid sequence of SEQ ID NO: 13, a light chain variable region CDR1 having the amino acid sequence of SEQ ID NO: 15, a light chain variable region CDR2 having the amino acid sequence of SEQ ID NO: 17, and a light chain variable region CDR3 having the amino acid sequence of SEQ ID NO: 19; and

wherein the monoclonal antibody or antigen binding fragment thereof specifically binds to an epitope within the LRP6 extracellular domain, wherein the LRP6 extracellular domain has the amino acid sequence of SEQ ID NO: 2.

16. The method of claim 15 , wherein the monoclonal antibody or antigen binding fragment thereof has:

a heavy chain variable region amino acid sequence that is at least 90% identical to SEQ ID NO: 5, and wherein the CDR1, CDR2, and CDR3 thereof are 100% identical to the amino acid sequences of SEQ ID NOS:9, 11, and 13, respectively; and

a light chain variable region amino acid sequence that is at least 90% identical to SEQ ID NO: 7, and wherein the CDR1, CDR2, and CDR3 thereof are 100% identical to the amino acid sequences of SEQ ID NOS:15, 17, and 19, respectively.

17. The method of claim 15 , wherein the monoclonal antibody or antigen binding fragment thereof is selected from the group consisting of a full length immunoglobulin molecule, an scFv, a Fab fragment, an Fab′ fragment, an F(ab′)2, an Fv, a disulfide linked Fv, and combinations thereof.

18. The method of claim 15 , wherein the monoclonal antibody or antigen binding fragment thereof is humanized.

19. The method of claim 15 , wherein the monoclonal antibody or antigen binding fragment thereof binds to the LRP6 extracellular domain with a dissociation constant of less than or equal to about 10 −7 M.

20. The method of claim 15 , wherein the monoclonal antibody or antigen binding fragment thereof binds to the same epitope as the antibody produced by the hybridoma having ATCC Designation No. PTA-10663.

21. The method of claim 15 , wherein the monoclonal antibody or antigen binding fragment thereof inhibits the binding of both Wnt1 and Wnt3a to LRP6.

22. The method of claim 15 , wherein the cell is further defined as the hybridoma having ATCC Designation No. PTA-10663.

23. A method of producing a monoclonal antibody or antigen binding fragment thereof, comprising the step of:

culturing a cell that produces the monoclonal antibody or antigen binding fragment thereof of claim 14 under conditions that permit production of the monoclonal antibody or antigen binding fragment thereof.

24. An isolated monoclonal antibody or antigen binding fragment thereof, wherein the monoclonal antibody or antigen binding fragment thereof specifically binds to an epitope within the LRP6 extracellular domain, and wherein the LRP6 extracellular domain has the amino acid sequence of SEQ ID NO: 2, wherein at least one of:

(a) the monoclonal antibody or antigen binding fragment thereof comprises:

(i) a light chain variable region CDR1 having the amino acid sequence of SEQ ID NO: 15;

(ii) a light chain variable region CDR2 having the amino acid sequence of SEQ ID NO: 17;

(iii) a light chain variable region CDR3 having the amino acid sequence of SEQ ID NO: 19;

(iv) a heavy chain variable region CDR1 having the amino acid sequence of SEQ ID NO: 9;

(v) a heavy chain variable region CDR2 having the amino acid sequence of SEQ ID NO: 11; and

(vi) a heavy chain variable region CDR3 having the amino acid sequence of SEQ ID NO: 13;

(b) the monoclonal antibody or antigen binding fragment thereof is produced by the hybridoma having ATCC Designation No. PTA-10663;

(c) the monoclonal antibody or antigen binding fragment thereof comprises a heavy chain and light chain variable region, wherein the heavy chain has the amino acid sequence of SEQ ID NO:5; and

(d) the monoclonal antibody or antigen binding fragment thereof comprises a light chain and heavy chain variable region, wherein the light chain has the amino acid sequence of SEQ ID NO:7.

25. A method of producing a monoclonal antibody or antigen binding fragment thereof, comprising the step of:

culturing a cell that produces the monoclonal antibody or antigen binding fragment thereof of claim 24 under conditions that permit production of the monoclonal antibody or antigen binding fragment thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 9, 2012
From: UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027677/0655 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2011
From: MA, JIAN-XING; LEE, KYUNGWON; CHEN, YING
To: THE BOARD OF REGENTS OF THE UNIVERSITY OF OKLAHOMA
Reel/Frame 025840/0133 →
Continuity (2)
Provisional Application 61306083 · Feb 19, 2010
Related Publication 20120045437A1 · Feb 23, 2012