Epithelial membrane protein-2 (EMP2) and proliferative vitroretinopathy (PVR)

Patent metadata

Field	Value
Publication number	US-9464135-B2
Application number	US-201013510877-A
Country	US
Kind code	B2
Filing date	Nov 18, 2010
Priority date	Oct 8, 2007
Publication date	Oct 11, 2016
Grant date	Oct 11, 2016

Abstract

Methods of preventing retinal detachment associated with proliferative vitreoretinopathy are provided by administering agents which antagonize the activity or function of EMP2 to subjects at risk of the detachment.

First claim

What is claimed is:

1. A method of reducing or inhibiting proliferative vitreoretinopathy or retinal detachment associated with traumatic injury, surgery or aberrant wound healing in a human subject, said method comprising administering an anti-EMP2 (Epithelial Membrane Protein-2) antibody that binds to EMP2 in the human subject, wherein the antibody comprises a heavy chain variable region comprising heavy chain three complementary-determining regions (CDR1-3) and a light chain variable region comprising three light chain complementary determining regions (CDR1-3), wherein:
the sequence of heavy chain CDR1 of the antibody is SYAMH (SEQ ID NO: 12),
the sequence of heavy chain CDR2 of the antibody is VISYDGSNKYYADSVKG (SEQ ID NO: 13),
the sequence of heavy chain CDR3 of the antibody is DRRGRKSAGIDY (SEQ ID NO: 14),
the sequence of light chain CDR1 of the antibody is QASQDISNYLN (SEQ ID NO: 15),
the sequence of light chain CDR2 of the antibody is AASSLQS (SEQ ID NO: 16), and
the sequence of light chain CDR3 of the antibody is LQDYNGWT (SEQ ID NO: 17),
or
the sequence of heavy chain CDR1 of the antibody is SYAMH (SEQ ID NO: 12),
the sequence of heavy chain CDR2 of the antibody is VISYDGSNKYYADSVKG (SEQ ID NO: 13),
the sequence of heavy chain CDR3 of the antibody is TVGATGAFDI (SEQ ID NO: 18),
the sequence of light chain CDR1 of the antibody is RASQSIGKWLA (SEQ ID NO: 19),
the sequence of light chain CDR2 of the antibody is KASSLEG (SEQ ID NO: 20), and
the sequence of light chain CDR3 of the antibody is QQSHNFPPT (SEQ ID NO: 21);
wherein the anti-EMP2 antibody is a monoclonal antibody, a humanized antibody, or a chimeric antibody, a diabody, a minibody, a Fv fragment, a F(ab′) fragment, or a F(ab′) 2 fragment; and
wherein the administering of the anti-EMP2 antibody reduces or inhibits proliferative vitreoretinopathy or retinal detachment associated with traumatic injury, surgery or aberrant wound healing in the subject.

2. The method of claim 1 , wherein the anti-EMP2 agent is locally administered.

3. The method of claim 1 , wherein the administration is directly to the eye.

4. The method of claim 1 , wherein the anti-EMP2 antibody is administered intraocularly.

5. The method of claim 1 , wherein the anti-EMP2 antibody is injected into the vitreous humor of the eye.

6. The method of claim 1 , wherein the anti-EMP2 antibody specifically binds to an EMP2 polypeptide having the amino acid sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, and SEQ ID NO:30.

7. The method of claim 1 , wherein the antibody is a monoclonal antibody.

8. The method of claim 1 , wherein the antibody is a humanized monoclonal antibody.

9. The method of claim 1 , wherein the antibody is a diabody or a minibody.

10. The method of claim 1 , wherein the antibody is a Fv, F(ab′) or F(ab′)2 fragment.

11. The method of claim 1 , wherein the antibody is a chimeric antibody having a murine antigen-binding site and a humanized region that regulates effector function.

12. The method of claim 1 , wherein the antibody is coupled to a cytotoxic agent.

13. The method of claim 1 , wherein administration of the anti-EMP2 antibody reduces the risk of a retinal detachment.

14. The method of claim 1 , wherein the anti-EMP2 antibody is formulated for injection into the eye.

15. The method of claim 1 , wherein the anti-EMP2 antibody is formulated for local administration external to the eye.

16. The method of claim 1 , wherein the vitreoretinopathy is rhegmatogenous vitreoretinopathy.

17. The method of claim 1 , wherein prior to administration of the anti-EMP2 antibody, the eye suffered a traumatic injury or a surgery contributing to the risk of retinal detachment.

18. The method of claim 1 wherein:
the sequence of heavy chain CDR1 of the antibody is SYAMH (SEQ ID NO: 12),
the sequence of heavy chain CDR2 of the antibody is VISYDGSNKYYADSVKG (SEQ ID NO: 13),
the sequence of heavy chain CDR3 of the antibody is DRRGRKSAGIDY (SEQ ID NO: 14),
the sequence of light chain CDR1 of the antibody is QASQDISNYLN (SEQ ID NO: 15),
the sequence of light chain CDR2 of the antibody is AASSLQS (SEQ ID NO: 16), and
the sequence of light chain CDR3 of the antibody is LQDYNGWT (SEQ ID NO: 17).

19. The method of claim 1 wherein:
the sequence of heavy chain CDR1 is SYAMH (SEQ ID NO: 12),
the sequence of heavy chain CDR2 is VISYDGSNKYYADSVKG (SEQ ID NO: 13),
the sequence of heavy chain CDR3 is TVGATGAFDI (SEQ ID NO: 18),
the sequence of light chain CDR1 is RASQSIGKWLA (SEQ ID NO: 19),
the sequence of light chain CDR2 is KASSLEG (SEQ ID NO: 20), and
the sequence of light chain CDR3 is QQSHNFPPT (SEQ ID NO: 21).

20. A method of reducing or inhibiting proliferative vitreoretinopathy or retinal detachment associated with traumatic injury, surgery or aberrant wound healing in a human subject, said method comprising administering an anti-EMP2 (Epithelial Membrane Protein-2) antibody that binds to EMP2 in the human subject, wherein:
the sequence of heavy chain is the sequence of SEQ ID NO: 4, and
the sequence of light chain is the sequence of SEQ ID NO: 5,
or
the sequence of heavy chain is the sequence of SEQ ID NO: 6, and
the sequence of light chain is the sequence of SEQ ID NO: 7;
wherein the anti-EMP2 antibody is a monoclonal antibody, a humanized antibody, or a chimeric antibody, a diabody, a minibody, a Fv fragment, a F(ab′) fragment, or a F(ab′) 2 fragment; and
wherein the administering of the anti-EMP2 antibody reduces or inhibits proliferative vitreoretinopathy or retinal detachment associated with traumatic injury, surgery or aberrant wound healing in the subject.

Assignees

• Gordon Lynn K
• Morales Shawn A
• Telander David
• Braun Jonathan
• Univ California
• The United States Of America Dept Of Veteran Affairs

Inventors

• Gordon Lynn K
• Morales Shawn A
• Telander David
• Braun Jonathan

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P27/02

  Ophthalmic agents · CPC title

• A61P27/00

  Drugs for disorders of the senses · CPC title

• A61K9/0048

  Eye, e.g. artificial tears · CPC title

• A61K2039/505

  comprising antibodies · CPC title