IP Library Granted Patent US 7,189,697
Granted Patent B2
US 7,189,697 · App. 11/104,677 · Granted Mar 13, 2007

Compositions and uses of a galectin for treatment of dry eye syndrome

Assignee: Trustees of Tufts College
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Quick Facts
Patent No.
US 7,189,697
App. No.
11/104,677
Granted
Mar 13, 2007
Kind
B2
Abstract

Methods for the therapeutic treatment of dry eye in mammals comprising administering to a mammal afflicted with an epithelial wound a therapeutically effective amount of a galectin-1 protein, a galectin-3, a galectin-7 protein and/or a galectin-8 protein are provided. Pharmaceutical and ophthalmic compositions and kits, comprising a pharmaceutically an active agent which is a galectin-1 protein, a galectin-3 protein, galectin-7 protein and/or a galectin-8 protein, and a suitable carrier or a diluent, are provided.

Claims (26)

1. A method for treating or preventing dry eye syndrome in a mammal in need thereof, comprising administering to the mammal a therapeutically effective amount of a galectin protein.

2. The method according to claim 1 , further comprising prior to administering, identifying the mammal in need of preventing dry eye syndrome.

3. The method according to claim 1 , wherein the mammal in need of treating or preventing dry eye syndrome is characterized by at least one condition selected from the group consisting of: ocular epithelial wounds; prior usage of anti-histamine agents; prior usage of anti-inflammatory agents; and prior usage of excimer laser treatment.

4. The method according to claim 1 , wherein the mammal is a human.

5. The method according to claim 1 , wherein the galectin protein is selected from the group consisting of galectin-1, galectin-3, galectin-7, galectin-8 and combinations thereof.

6. The method according to claim 5 , wherein the dry eye is a persistent syndrome.

7. The method according to claim 5 , wherein the dry eye results in epithelial erosion.

8. The method according to claim 7 , wherein the epithelial erosion produces a corneal wound.

9. The method according to claim 5 , wherein the galectin-8 protein comprises the amino acid sequence of SEQ ID NO: 4 or 5.

10. The method according to claim 5 , wherein the galectin-8 protein comprises an amino acid sequence that is substantially identical to the amino acid sequence of SEQ ID NO: 4 or 5.

11. The method according to claim 10 , wherein substantially identical is having at least 60% identity, at least 70% identity, at least 80% identity, or at least 90% identity to the amino acid sequence of SEQ ID NO: 4 or 5.

12. The method according to claim 5 , wherein the galectin-8 protein comprises a galectin-8 N-terminal domain and a galectin-8 proline, glycine, and tyrosine-rich domain and a galectin-8 galactoside-binding domain.

13. The method according to claim 5 , wherein the galectin-3 protein comprises a galectin-3 proline, glycine, and tyrosine-rich domain and a galectin-3 galactoside-binding domain.

14. The method according to claim 5 , wherein the galectin-7 protein comprises a galectin-7 N-terminal domain and a galectin-7 proline, glycine, and tyrosine-rich domain and a galectin-7 galactoside-binding domain.

15. The method according to claim 5 , wherein the galectin-1 protein comprises a galectin-1 N-terminal domain and a galectin-1 proline, glycine, and tyrosine-rich domain and a galectin-1 galactoside-binding domain.

16. The method according to claim 5 , wherein the galectin-7 protein comprises the amino acid sequence of SEQ ID NO: 2.

17. The method according to claim 5 , wherein the galectin-7 protein comprises an amino acid sequence that is substantially identical to the amino acid sequence of SEQ ID NO: 2.

18. The method according to claim 17 , wherein substantially identical is having at least 70% identity, at least 80% identity, or least 90% identity to the amino acid sequence of SEQ ID NO: 2.

19. The method according to claim 5 , wherein the galectin-3 protein comprises the amino acid sequence of SEQ ID NO: 1.

20. The method according to claim 5 , wherein the galectin-3 protein comprises an amino acid sequence that is substantially identical to the amino acid sequence of SEQ ID NO: 1.

21. The method according to claim 20 , wherein substantially identical is having at least 70% identity, at least 80% identity, or least 90% identity to the amino acid sequence of SEQ ID NO: 1.

22. The method according to claim 5 , wherein the galectin-3 protein comprises a galectin-3 galactoside-binding domain.

23. The method according to claim 5 , wherein the galectin-1 protein comprises the amino acid sequence of SEQ ID NO: 6.

24. The method according to claim 5 , wherein the galectin-1 protein comprises an amino acid sequence that is substantially identical to the amino acid sequence of SEQ ID NO: 6.

25. The method according to claim 24 , wherein substantially identical is having at least 60% identity, at least 70% identity, at least 80% identity, or least 90% identity to the amino acid sequence of SEQ ID NO: 6.

26. The method according to claim 5 , wherein the galectin-1 protein comprises a galectin-1 galactoside-binding domain.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 5, 2012
From: TUFTS UNIVERSITY BOSTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029244/0633 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2006
From: PANJWANI, NOORJAHAN
To: TRUSTEES OF TUFTS COLLEGE
Reel/Frame 018495/0067 →
Continuity (3)
Provisional Application 6063436100 · Dec 8, 2004
Provisional Application 6056203000 · Apr 13, 2004
Related Publication 20060189514A1 · Aug 24, 2006