IP Library Granted Patent US 8,877,722
Granted Patent B2
US 8,877,722 · App. 13/072,017 · Granted Nov 4, 2014

Compositions for inhibiting gene expression and uses thereof

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Quick Facts
Patent No.
US 8,877,722
App. No.
13/072,017
Granted
Nov 4, 2014
Kind
B2
Abstract

The inventors have examined the means for providing more efficacious miRNA blocking compounds. The inventors have discovered new structural features that surprisingly improve the efficacy of miRNA blocking molecules. These features include the presence of multiple 3′ ends and a linker at the 5′ ends. Surprisingly, these features improve the efficacy of the gene expression blocking compounds in a manner that decreases the compound's biologic instability. Even more surprisingly, this effect has been found to be applicable to both DNA and RNA oligonucleotide-based compounds and to have application in traditional antisense and RNAi technology.

Claims (10)

1. A method for inhibiting miRNA activity, the method comprising contacting a cell with a synthetic oligonucleotide-based compound comprising two single stranded oligonucleotides that are complementary to a miRNA sequence, wherein the oligonucleotides are linked at their 5′-ends, such that the oligonucleotide-based compound has two accessible 3′-ends and the oligonucleotides specifically hybridize to and inhibit the activity of the miRNA sequence.

2. A method for inhibiting in vivo miRNA activity, the method comprising administering to a mammal an oligonucleotide-based compound comprising two single stranded oligonucleotides that are complementary to a miRNA sequence, wherein the oligonucleotides are linked at their 5′-ends, such that the oligonucleotide-based compound has two accessible 3′-ends and the oligonucleotides specifically hybridize to and inhibit the activity of the miRNA sequence.

3. The method according to claim 2 wherein the miRNA sequence is miR-21.

4. The method according to claim 2 wherein the route of administration is selected from parenteral, intramuscular, subcutaneous, intraperitoneal, intraveneous, mucosal delivery, oral, sublingual, transdermal, topical, inhalation, intranasal, aerosol, intraocular, intratracheal, intrarectal, vaginal, gene gun, dermal patch, eye drop or mouthwash.

5. The method according to claim 1 wherein the miRNA sequence is miR-21.

6. The method according to claim 2 , further comprising administering one or more vaccines, antigens, antibodies, cytotoxic agents, allergens, antibiotics, antisense oligonucleotides, TLR agonist, TLR antagonist, siRNA molecules, miRNA molecules, antisense oligonucleotides, aptamers, proteins, peptides, gene therapy vectors, adjuvants, kinase inhibitors, chemotherapeutic agents, targeted therapeutic agents, activated cells, co-stimulatory molecules or combinations thereof.

7. The method according to claim 2 , wherein the mammal is a human.

8. The method according to claim 6 , wherein the vaccine is a DNA vaccine, peptide vaccine, or protein vaccine.

9. The method according to claim 1 , further comprising contacting the cell with one or more vaccines, antigens, antibodies, cytotoxic agents, allergens, antibiotics, antisense oligonucleotides, TLR agonist, TLR antagonist, siRNA molecules, miRNA molecules, antisense oligonucleotides, aptamers, proteins, peptides, gene therapy vectors, adjuvants, kinase inhibitors, chemotherapeutic agents, targeted therapeutic agents, activated cells, co-stimulatory molecules or combinations thereof.

10. The method according to claim 9 , wherein the vaccine is a DNA vaccine, peptide vaccine, or protein vaccine.

Assignments (1)
SECURITY INTEREST Recorded Jul 28, 2023
From: ACERAGEN, INC.; ARREVUS, INC.
To: NOVAQUEST CO-INVESTMENT FUND XV, L.P.
Reel/Frame 064419/0493 →