IP Library Granted Patent US 8,592,571
Granted Patent B2
US 8,592,571 · App. 13/450,886 · Granted Nov 26, 2013

RNAi modulation of APOB and uses thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,592,571
App. No.
13/450,886
Granted
Nov 26, 2013
Kind
B2
Abstract

The invention relates to compositions and methods for modulating the expression of apolipoprotein B, and more particularly to the downregulation of apolipoprotein B by chemically modified oligonucleotides.

Claims (22)

1. An iRNA agent comprising a sense strand and an antisense strand, wherein said sense strand comprises a first sequence and said antisense strand comprises a second sequence, wherein said first sequence is complementary to said second sequence, wherein said second sequence is complementary to a segment of an Apolipoprotein B (ApoB) mRNA, wherein each strand of said iRNA agent is between 15 and 30 nucleotides in length, and wherein the second sequence comprises at least 15 contiguous nucleotides of the nucleotide sequence of SEQ ID NO:154.

2. The iRNA agent of claim 1 , further comprising a non-nucleotide moiety.

3. The iRNA agent of claim 1 , further comprising a phosphorothioate linkage.

4. The iRNA agent of claim 3 , wherein said iRNA agent comprises a phosphorothioate at the first and second internucleotide linkage at the 3′ end of the antisense strand.

5. The iRNA agent of claim 3 , wherein said iRNA agent comprises a phosphorothioate at the first internucleotide linkage at the 3′ end of the sense strand.

6. The iRNA agent of claim 1 , further comprising a 2′-modified nucleotide.

7. The iRNA agent of claim 6 , wherein the 2′-modification is chosen from the group of: 2′-deoxy, 2′-deoxy-2′-fluoro, 2′-O-methyl, 2′-O-methoxyethyl (2′-O-MOE), 2′-0-aminopropyl (2′-O-AP), 2′-0-dimethylaminoethyl (2′-O-DMAOE), 2′-dimethylaminopropyl (2′-O-DMAP), 2′-O-dimethylaminoethyloxyethyl (2′-O-DMAEOE), and 2′-O-N-methylacetamido (2′-O-NMA).

8. The iRNA agent of claim 6 , further comprising: at least one 5′-uridine-adenine-3′ (5′-UA-3′) dinucleotide wherein the uridine is a 2′-modified nucleotide; at least one 5′-uridine-guanine-3′ (5′-UG-3′) dinucleotide, wherein the 5′-uridine is a 2′-modified nucleotide; at least one 5′-cytidine-adenine-3′ (5′-CA-3′) dinucleotide, wherein the 5′-cytidine is a 2′-modified nucleotide; or at least one 5′-uridine-uridine-3′ (5′-UU-3′) dinucleotide, wherein the 5′-uridine is a 2′-modified nucleotide.

9. The iRNA agent of claim 8 , wherein the 5′-most pyrimidines in all occurrences of sequence motif 5′-UA-3′, 5′-CA-3′, 5′-UU-3′, and 5′-UG-3′ on the antisense strand are 2′-modified nucleotides.

10. The iRNA agent of claim 1 , wherein the first sequence comprises at least 15 contiguous nucleotides of the nucleotide sequence of SEQ ID NO:153.

11. The iRNA agent of claim 1 , wherein the second sequence comprises the nucleotide sequence of SEQ ID NO:154.

12. The iRNA agent of claim 1 , wherein a 5′-end of said iRNA agent comprises an adenosine, cytidine, guanosine, thymidine, or uridine.

13. The iRNA agent of claim 1 , further comprising a nucleotide overhang having 1 to 4 nucleotides.

14. The iRNA agent of claim 13 , wherein the nucleotide overhang has 2 or 3 unpaired nucleotides.

15. The iRNA agent of claim 13 , wherein the nucleotide overhang is at the 3′-end of the antisense strand of the iRNA agent.

16. The iRNA agent of claim 1 , further comprising a cholesterol moiety.

17. The iRNA agent of claim 16 , wherein the cholesterol moiety is conjugated to the 3′-end of the sense strand of the iRNA agent.

18. The iRNA agent of claim 1 , wherein said iRNA agent reduces the amount of ApoB mRNA present in cultured mouse cells of hepatic origin by an amount greater than a control iRNA agent.

19. The iRNA agent of claim 1 , wherein the agent reduces the amount of ApoB mRNA in cultured human HepG2 cells after incubation with the agent by more than 50% compared to cells that have not been incubated with the agent, or reduces the amount of ApoB protein secreted into cell culture supernatant by more than 50% compared to a control.

20. A method for reducing the expression levels of ApoB in a subject, comprising administering the iRNA agent of claim 1 to said subject.

21. The iRNA agent of claim 1 , wherein the first sequence comprises the nucleotide sequence of SEQ ID NO:153.

22. The iRNA agent of claim 1 , wherein the first sequence comprises the nucleotide sequence of SEQ ID NO:153 and the second sequence comprises the nucleotide sequence of SEQ ID NO:154.

Assignments (2)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2013
From: SOUTSCHEK, JUERGEN; VORNLOCHER, HANS-PETER; HADWIGER, PHILIPP; ELBASHIR, SAYDA
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 030927/0391 →