Compositions and Methods for Inhibiting Viral Replication

• US 20100316699A1
• Filed: 12/04/2009
• Published: 12/16/2010
• Est. Priority Date: 10/12/2001
• Status: Active Grant

• Current Assignee: Hans-Peter Vornlocher, Matthias John, Roland Kreutzer, Stefan Limmer
• Original Assignee: Hans-Peter Vornlocher, Matthias John, Roland Kreutzer, Stefan Limmer
• Inventors: Limmer, Stefan, John, Matthias, Vornlocher, Hans-Peter, Kreutzer, Roland
• Granted Patent: US 8,273,868 B2
• Time in Patent Office: Days
• US Class Current: 424/450
• CPC Class Codes: A61P 31/14 for RNA viruses
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: C12N 15/1131 against viruses
• CPC Class Codes: C12N 2310/14 interfering N.A.
• CPC Class Codes: C12N 2310/53 partially self-complementary or closed

Abstract

The present invention relates to a double-stranded ribonucleic acid (dsRNA) having a nucleotide sequence which is less that 30 nucleotides in length and which is substantially identical to at least a part of a 3′-untranslated region (3′-UTR) of a (+) strand RNA virus, such as HCV, as well as pharmaceutical compositions comprising the dsRNA, together with a pharmaceutically acceptable carrier. The pharmaceutical compositions are useful for treating infections and diseases caused by the replication or activity of the (+) strand RNA virus, as well as methods for inhibiting viral replication.

Claims

1. A double-stranded ribonucleic acid (dsRNA) for inhibiting the replication of a (+) strand RNA virus, wherein the dsRNA comprises a sense RNA strand consisting of a nucleotide sequence which is substantially identical to at least a part of a 3′

-untranslated region (3′

-UTR) of the (+) strand RNA virus and an antisense RNA strand which is complementary to at least a part of the sense RNA strand, and wherein each strand of the dsRNA is 21 to 24 nucleotides in length.

4. The dsRNA of claim 1, wherein the dsRNA comprises a blunt end.

5. The dsRNA of claim 1, wherein the dsRNA comprises two blunt ends.

6. The dsRNA of claim 1, wherein the antisense RNA strand and the sense RNA strand comprise a 3′

-terminus and a 5′

-terminus, and wherein at least one of said RNA strands comprises a nucleotide overhang of 1 to 3 nucleotides in length.

7. The dsRNA of claim 6, wherein the nucleotide overhang is two nucleotides in length.

8. The dsRNA of claim 6, wherein the nucleotide overhang is on the 3′

-terminus of the antisense RNA strand.

9. The dsRNA of claim 6, wherein the dsRNA further comprises a first end and a second end, wherein the first end comprises the 3′

-terminus of the antisense RNA strand and the 5′

-terminus of the sense RNA strand, and wherein the second end comprises the 5′

-terminus of the antisense RNA strand and the 3′

-terminus of the sense RNA strand, wherein the first end comprises a nucleotide overhang on the 3′

-terminus of the antisense RNA strand, and wherein the second end is blunt.

10. The dsRNA of claim 6, wherein the antisense RNA strand is 23 nucleotides in length and comprises a 2-nucleotide overhang at the 3′

-terminus, wherein the sense RNA strand is 23 nucleotides in length and comprises a 2-nucleotide overhang at the 3′

-terminus, and wherein the dsRNA has a 21-nucleotide double-stranded region.

2-3. -3. (canceled)

11. A pharmaceutical composition for inhibiting the replication of a (+) strand RNA virus in an mammal, comprising a dsRNA and a pharmaceutically acceptable carrier, wherein the dsRNA comprises a sense RNA strand consisting of a nucleotide sequence which is substantially identical to at least a part of a 3′

-untranslated region (3′

-UTR) of the (+) strand RNA virus and an antisense RNA strand which is complementary to at least a part of the sense RNA strand, and wherein each strand of the dsRNA is 21 to 24 nucleotides in length.

14. The pharmaceutical composition of claim 11, wherein the dsRNA comprises a blunt end.

15. The pharmaceutical composition of claim 11, wherein the dsRNA comprises two blunt ends.

16. The pharmaceutical composition of claim 11, wherein the antisense RNA strand and the sense RNA strand comprise a 3′

-terminus and a 5′

-terminus, and wherein at least one of said RNA strands comprise a nucleotide overhang of 1 to 3 nucleotides in length.

17. The pharmaceutical composition of claim 16, wherein the nucleotide overhang is two nucleotides in length.

18. The pharmaceutical composition of claim 16, wherein the nucleotide overhang is on the 3′

-terminus of the antisense RNA strand.

19. The pharmaceutical composition of claim 16, wherein the dsRNA further comprises a first end and a second end, wherein the first end comprises the 3′

-terminus of the antisense RNA strand and the 5′

-terminus of the sense RNA strand, and wherein the second end comprises the 5′

-terminus of the antisense RNA strand and the 3′

-terminus of the sense RNA strand, wherein the first end comprises a nucleotide overhang on the 3′

-terminus of the antisense RNA strand, and wherein the second end is blunt.

20. The pharmaceutical composition of claim 16, wherein the antisense RNA strand is 23 nucleotides in length and comprises a 2-nucleotide overhang at the 3′

-terminus, wherein the sense RNA strand is 23 nucleotides in length and comprises a 2-nucleotide overhang at the 3′

-terminus, and wherein the dsRNA has a 21-nucleotide double-stranded region.

21. The pharmaceutical composition of claim 11, wherein a dosage unit of dsRNA is less than 5 milligram (mg) of dsRNA per kg body weight of the mammal.

22. The pharmaceutical composition of claim 11, wherein a dosage unit of dsRNA is in a range of 0.01 to 2.5 milligrams (mg), 0.1 to 200 micrograms (μ

g), 0.1 to 100 μ

g per kilogram body weight of the mammal.

23. The pharmaceutical composition of claim 11, wherein a dosage unit of dsRNA is less than 25 μ

g per kilogram body weight of the mammal.

24. The pharmaceutical composition of claim 11, wherein the pharmaceutically acceptable carrier is an aqueous solution.

25. The pharmaceutical composition of claim 24, wherein the aqueous solution is phosphate buffered saline.

26. The pharmaceutical composition of claim 11, wherein the pharmaceutically acceptable carrier comprises a micellar structure selected from the group consisting of a liposome, capsid, capsoid, polymeric nanocapsule, and polymeric microcapsule.

27. The pharmaceutical composition of claim 11, which is formulated to be administered by inhalation, infusion, injection, or orally.

28. The pharmaceutical composition of claim 11, which is formulated to be administered by intravenous or intraperitoneal injection.

12-13. -13. (canceled)