IP Library Granted Patent US 10,174,321
Granted Patent B2
US 10,174,321 · App. 15/538,964 · Granted Jan 8, 2019

RNAI induced huntingtin gene suppression

Inventors: Pavlina Stefanova Konstantinova (Amsterdam, NL); Jana Miniariková (Amsterdam, NL)
Assignee: UNIQURE IP B.V.
C12N15/113A61K31/713C12N2310/14C12N2310/141C12N2310/3519C12N2310/531C12N2320/32C12N2330/51
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Quick Facts
Patent No.
US 10,174,321
App. No.
15/538,964
Granted
Jan 8, 2019
Kind
B2
Abstract

The present invention provides for a double stranded RNA comprising a first RNA sequence and a second RNA sequence wherein the first and second RNA sequence are substantially complementary, wherein the first RNA sequence has a sequence length of at least 19 nucleotides and is substantially complementary to SEQ ID NO. 1. Said double stranded RNA is for use in inducing RNAi against Huntingtin exon 1 sequences. The double stranded RNA of to the invention was capable of reducing neuronal cell death and huntingtin aggregates in an animal model.

Claims (15)

1. A double stranded RNA comprising a first RNA sequence and a second RNA sequence wherein the first and second RNA sequence are substantially complementary, wherein the first RNA sequence has a sequence length of at least 19 nucleotides and is fully complementarity to SEQ ID NO. 1.

2. A double stranded RNA according to claim 1 , wherein said double stranded RNA is capable of reducing huntingtin gene expression.

3. A double stranded RNA according to claim 1 , wherein the double stranded RNA is comprised in a pre-miRNA scaffold, a pri-miRNA scaffold, a shRNA, or an siRNA, preferably a pre-miRNA scaffold.

4. A double stranded RNA according to claim 1 , wherein the first RNA sequence has a sequence length of at least 20 nucleotides, preferably of at least 21 nucleotides.

5. A double stranded RNA according to claim 1 , wherein the first strand is selected from the group consisting of SEQ ID NO.3, SEQ ID NO.4, SEQ ID NO.5, SEQ ID NO.6, and SEQ ID NO.7.

6. A double stranded RNA according to claim 1 , wherein the first strand and second strand are selected from the group consisting of the combinations of SEQ ID NO. 3 and 8; SEQ ID NO. 4 and 9; SEQ ID NO. 5 and 10; SEQ ID NO. 5 and 13; SEQ ID NO. 5 and 14; SEQ ID NO. 6 and 11; and SEQ ID NO. and 7 and 12.

7. A double stranded RNA according to claim 1 , wherein the double stranded RNA is comprised in a pre-miRNA scaffold derived from miR-451a or miR-155.

8. A DNA sequence encoding the double stranded RNA according to claim 1 .

9. An expression cassette encoding the double stranded RNA according to claim 1 .

10. An expression cassette according to claim 9 , wherein the expression cassette comprises the PGK promoter, a CMV promoter, a neurospecific promoter or a CBA promoter.

11. A gene therapy vector comprising the expression cassette according to claim 9 .

12. A gene therapy vector according to claim 11 , wherein the gene therapy vector is an AAV vector, preferably an AAV vector of serotype 5.

13. A host cell comprising the DNA sequence according to claim 8 or the expression cassette according to claim 9 .

14. A method of treating Huntington's disease comprising, administering to an individual with Huntington's disease the double stranded RNA according to claim 1 .

15. A method of treating Huntington's disease comprising, administering to an individual with Huntington's disease the expression cassette according to claim 9 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2017
From: KONSTANTINOVA, PAVLINA STEFANOVA; MINIARIKOVÁ, JANA
To: UNIQURE IP B.V.
Reel/Frame 043543/0270 →
Priority Claims (1)
EP 14200308 · Dec 24, 2014 · regional
Continuity (1)
Related Publication 20170355989A1 · Dec 14, 2017
Cited By (1)
US 12,709,748