Compositions and methods for treating diabetic retinopathy

Patent metadata

Field	Value
Publication number	US-10870852-B2
Application number	US-201615765736-A
Country	US
Kind code	B2
Filing date	Oct 6, 2016
Priority date	Oct 6, 2015
Publication date	Dec 22, 2020
Grant date	Dec 22, 2020

Abstract

The application discloses compositions and methods for preventing and treating diabetic retinopathy. It is disclosed herein that an inhibitor of microRNA-let-7b administered to the eye of a subject in need thereof is useful for preventing and treating several problems associated with diabetic retinopathy and plays a role in vasculature stabilization, increasing retinal thickness, reducing retinal capillary dropout, diminishing microvascular leakage, preventing or treating hyperproliferation of microvascular cells, and stabilizing aberrant neovascularization. The invention includes the use of various kinds of inhibitors of microRNA-let-7b, including, but not limited to, an antagomir of miRNA-let-7b. A useful compound of the invention can be administered into the eye, including intravitreally. A useful antagomir is Dy547-mA(*)mA(*)mCmCmAmCmAmCmAmAmCmCmUmAmCmUmAmCmCmU(*) mC(*)mA (*)(3′-Chl).

First claim

What is claimed is:

1. A method for treating a retinopathy, said method comprising providing a subject suffering from a retinopathy in which stabilization of vasculature in an eye of the subject is desired; and intravitreally administering to the subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an effective amount of an inhibitor of micro RNA (miRNA) let-7b levels or activity.

2. The method of claim 1 , wherein said inhibitor is a nucleic acid.

3. The method of claim 2 , wherein said nucleic acid is an antagomir of miRNA let-7b.

4. The method of claim 2 , wherein said nucleic acid comprises the sequence SEQ ID NO:1 or a biologically active homolog or fragment thereof.

5. The method of claim 4 , wherein said nucleic acid comprising the sequence SEQ ID NO:1 or a biologically active homolog of fragment thereof is modified.

6. The method of claim 5 , wherein said modification is selected from the group consisting of a detectable label, phosphorothioate modification, 2′-O-methyl modification, 2′-O-methoxyethyl modification, 3′-cholesterol (chl) modification, and locked nucleic acid (LNA) modification.

7. The method of claim 5 , wherein said nucleic acid comprises at least two modifications.

8. The method of claim 6 , wherein said nucleic acid comprises at least one phosphorothioate modification.

9. The method of claim 6 , wherein said nucleic acid comprises at least one 2′-O-methyl modification.

10. The method of claim 6 , wherein said nucleic acid comprises at least one 2′-O-methoxyethyl modification.

11. The method of claim 6 , wherein said nucleic acid comprises a 3′-chl modification.

12. The method of claim 6 , wherein said nucleic acid comprises at least one LNA modification.

13. The method of claim 6 , wherein said nucleic acid comprises a detectable label.

14. The method of claim 8 , wherein said nucleic acid comprises five phosphorothioate modifications.

15. The method of claim 9 , wherein said nucleic acid comprises a 2′-O-methyl modification at each nucleotide residue.

16. The method of claim 12 , wherein said nucleic acid comprises an LNA at each nucleotide residue.

17. The method of claim 5 , wherein said fragment is SEQ ID NO:2 or a modification thereof.

18. The method of claim 1 , wherein said inhibitor is selected from the group consisting of Antagomir-let7b which comprises Dy547 mA(*)mA(*)mCmCmAmCmAmCmAmAmCmCmUmAmCmUmAmCmCmU(*)mC(*)mA(*) (3′-Chl), LNA-Chl anti-sense let-7b which comprises IAIAICICIAICIAICIAIAICICIUIAICIUIAICICIUICIA(3′-Chl), LNA anti-sense let-7b which comprises IAIAICICIAICIAICIAIAICICIUIAICIUIAICICIUICIA, MOE anti-sense let-7b which comprises meAmeAmeCmeCmeAmeCmeAmeCmeAmeAmeCmeCmeUmeAmeCmeUmeAmeCme CmeUmeCmeA, Antagomir let-7b mini (truncated version) which comprises mA(*)mA(*)mCmCmAmCmAmCmAmAmCmC(*)mU(*)mA(3′-Chl), LNA-Chl anti-sense let-7b mini which comprises IAIAICICIAICIAICIAIAICICIUIA (3′-Chl), LNA anti-sense let-7b mini which comprises IAIAICICIAICIAICIAIAICICIUIA, and MOE anti-sense let-7b mini which comprises meAmeAmeCmeCmeAmeCmeAmeCmeAmeAmeCmeCmeUmeA, wherein Dy547 is a fluorescent molecule; “m” indicates 2-O-Methyl moiety; * indicates phosphorothioate; (3′-Chl) indicates a cholesterol molecule at the 3′; “I” indicates LNA modification; and “me” indicates 2′-O-methoxyethyl modification.

19. The method of claim 1 , wherein said method stimulates vascular stabilization and an increase in retinal thickness.

20. The method of claim 1 , wherein said method reduces hyperproliferation of microvascular cells, retinal capillary dropout, and microvascular leakage.

21. The method of claim 1 , wherein said retinopathy is diabetic retinopathy.

22. A method for inhibiting the effects of increased levels or activity of miRNA let-7b in a subject in need thereof, wherein said increased levels or activity are associated with a microvasculature injury, disease, or disorder of the eye, said method comprising providing a subject in which stabilization of vasculature in an eye of the subject is desired; and intravitreally administering to said subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and an effective amount of an inhibitor of miRNA let-7b levels or activity.

23. The method of claim 22 , wherein said inhibitor is a nucleic acid comprising the sequence SEQ ID NO:1 or a biologically active homolog or fragment thereof and said sequence is modified.

24. The method of claim 22 , wherein said increased levels or activity of miRNA let-7b are associated with diabetic retinopathy.

Assignees

• Univ Virginia Patent Foundation

Inventors

• Dey Bijan K
• Yates Paul Andrew

Classifications

• A61K31/7125

  Nucleic acids or oligonucleotides having modified internucleoside linkage, i.e. other than 3'-5' phosphodiesters · CPC title

• C12Q2600/178

  miRNA, siRNA or ncRNA · CPC title

• C12Q1/6883

  for diseases caused by alterations of genetic material · CPC title

• C12N2310/322

  2'-R Modification · CPC title

• C12Q2600/106

  Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism · CPC title