Method of use of antagonists of zonulin to prevent the loss of or to regenerate pancreatic cells

• US 20060287233A1
• Filed: 06/09/2006
• Published: 12/21/2006
• Est. Priority Date: 06/09/2005
• Status: Abandoned Application

• Current Assignee: Alessio Fasano, Anna Sapone, Blake Paterson
• Original Assignee: Alessio Fasano, Anna Sapone, Blake Paterson
• Inventors: Sapone, Anna, Fasano, Alessio, Paterson, Blake
• Application Number:
  US11/449,628
• Publication Number:
  US 20060287233A1
• Time in Patent Office: Days
• US Class Current: 514/6.900
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 35/39 Pancreas; Islets of Langerhans Langerhans cells of epidermis A61K35/36
• CPC Class Codes: A61K 38/08 Peptides having 5 to 11 amino acids A61K38/043 - A61K38/046 take precedence
• CPC Class Codes: A61K 38/18 Growth factors; Growth regulators
• CPC Class Codes: A61P 1/18 for pancreatic disorders, e.g. pancreatic enzymes
• CPC Class Codes: A61P 3/10 for hyperglycaemia, e.g. antidiabetics
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: A61P 5/00 Drugs for disorders of the endocrine system
• CPC Class Codes: A61P 5/50 for increasing or potentiating the activity of insulin

Abstract

The present invention provides materials and methods for the treatment of diabetes. Using the materials and methods of the invention, the loss of pancreatic β-cells can be slowed and/or prevented. In addition, the materials and methods of the invention can be used to regenerate pancreatic β-cells.

Claims

1. A method of slowing the loss of pancreatic β

-cells in a subject in need thereof, comprising;

administering to the subject a composition comprising an antagonist of zonulin.

2. A method according to claim 1, wherein the composition further comprises a factor that enhances cell growth.

3. A method according to claim 2, wherein the factor is a growth factor.

4. A method according to claim 2, wherein the factor is selected from a group consisting of epidermal growth factor (EGF), basic fibroblast growth factor-2 (BFGF-2), keratinocyte growth factor (KGF), hepatocyte growth factor/scatter factor (HGF/SF), glucagon-like-peptide-1 (GLP-1), exendin-4, islet/duodenum homeobox-1 (IDX-1), β

-cellulin, activin A, transforming growth factor-α

(TGF-α

), transforming growth factor-β

(TGF-β

), gastrin, and combinations thereof.

5. A method of regenerating pancreatic β

-cells in a subject in need thereof, comprising;

administering to the subject a zonulin antagonist and a cell.

6. A method according to claim 5, wherein the cell is an islet cell.

7. A method according to claim 5, wherein the cell is a β

-cell.

8. A method according to claim 5, wherein the cell is a stem cell.

9. A method according to claim 5, wherein the antagonist and the cell are administered simultaneously.

10. A method according to claim 5, wherein the antagonist and the cell are not administered simultaneously.

11. A method according to claim 5, further comprising administering a factor that enhances cell growth.

12. A method according to claim 11, wherein the factor is a growth factor.

13. A method according to claim 12, wherein the factor is selected from a group consisting of epidermal growth factor (EGF), basic fibroblast growth factor-2 (BFGF-2), keratinocyte growth factor (KGF), hepatocyte growth factor/scatter factor (HGF/SF), glucagon-like-peptide-1 (GLP-1), exendin-4, islet/duodenum homeobox-1 (IDX-1), β

-cellulin, activin A, transforming growth factor-α

(TGF-α

), transforming growth factor-β

(TGF-β

), gastrin, and combinations thereof.

14. A method of regenerating pancreatic β

-cells in a subject in need thereof, comprising;

administering to the subject a zonulin antagonist under conditions permitting replication of β

-cells.

15. A method according to claim 14, further comprising administering a factor that enhances cell growth.

16. A method according to claim 14, wherein the factor is a growth factor.

17. A method according to claim 14, wherein the factor is selected from a group consisting of epidermal growth factor (EGF), basic fibroblast growth factor-2 (BFGF-2), keratinocyte growth factor (KGF), hepatocyte growth factor/scatter factor (HGF/SF), glucagon-like-peptide-1 (GLP-1), exendin-4, islet/duodenum homeobox-1 (IDX-1), β

-cellulin, activin A, transforming growth factor-α

(TGF-α

), transforming growth factor-β

(TGF-β

), gastrin, and combinations thereof.

18. A method of regenerating pancreatic β

-cells in a subject in need thereof, comprising;

administering to the subject a zonulin antagonist; and

implanting cells into the subject.

19. A method according to claim 18, wherein the cells are islet cells.

20. A method according to claim 18, wherein the cells are β

-cells.

21. A method according to claim 18, wherein the cells are stem cells.

22. A method according to claim 18, wherein the antagonist is administered to the subject before the cells are implanted.

23. A method according to claim 18, wherein the antagonist is administered to the subject after the cells are implanted.

24. A method according to claim 18, wherein the antagonist is administered to the subject both before and after the cells are implanted.

25. A method according to claim 18, further comprising administering a factor that enhances cell growth.

26. A method according to claim 18, wherein the factor is a growth factor.

27. A method according to claim 18, wherein the factor is selected from a group consisting of epidermal growth factor (EGF), basic fibroblast growth factor-2 (BFGF-2), keratinocyte growth factor (KGF), hepatocyte growth factor/scatter factor (HGF/SF), glucagon-like-peptide-1 (GLP-1), exendin-4, islet/duodenum homeobox-1 (IDX-1), β

-cellulin, activin A, transforming growth factor-α

(TGF-α

), transforming growth factor-β

(TGF-β

), gastrin, and combinations thereof.

28. A method according to claim 25, wherein the factor is administered to the subject before the cells are implanted.

29. A method according to claim 25, wherein the factor is administered to the subject after the cells are implanted.

30. A method according to claim 25, wherein the factor is administered to the subject both before and after the cells are implanted.

31. A method of treating an autoimmune disease, comprising:

administering a compound that prevents an increase in permeability of an anatomical barrier.

32. The method of claim 31, wherein the compound that prevents an increase in the permeability of an anatomical barrier is an antagonist of a normal physiological compound that increases the permeability of the anatomical barrier.

33. The method of claim 31, wherein the compound is a zonulin antagonist.

34. The method of claim 33, wherein the zonulin antagonist comprises SEQ ID NO:

15.

35. The method of claim 31, wherein the compound is selected from the group consisting of SEQ IDs 1-24.