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US7307067B2 Expired / Lapsed US ⏱️ 0.0 years remaining

Methods and compositions for reducing viral genome amounts in a target cell

Assignee: Leland Stanford Junior University
•
Filing: 2005-05-03
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Granted: 2007-12-11
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Expires: 2025-05-03
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Abstract

Abstract Methods and compositions for reducing viral genome amounts in a target cell are provided. In the subject methods, the activity of a miRNA is inhibited in a manner sufficient to reduce the amount of viral genome in the target cell, e.g., by introducing a miRNA inhibitory agent in the target cell. Also provided are pharmaceutical compositions, kits and systems for use in practicing the subject methods. The subject invention finds use in a variety of applications, including the treatment of subjects suffering from a viral mediated disease condition, e.g., an HCV mediated disease condition.

Inventors

  • 👤 Peter Sarnow
  • 👤 Catherine L. Jopling
  • 👤 Alissa M. Lancaster

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 21:05
CPC Classifications
C; C12; C12N; C12N15/00; C12N15/09; C12N15/11; C12N15/113; C12N15/1131; A; A61; A61K; A61K31/00; A61K31/70; A61K31/7088; A61K45/00; A61K45/06; A61K9/00; A61K9/0012; A61K9/0019; A61P; A61P1/00; A61P1/16; A61P31/00; A61P31/12; A61P31/14; A61P31/20; A61P43/00; C12N15/111; C12N2310/00; C12N2310/10; C12N2310/11; C12N2310/113; C12N2310/14; C12N2310/141; C12N2310/30; C12N2310/32; C12N2310/321; C12N2320/00; C12N2320/30; C12N2320/31; C12N2320/50; C12N2330/00; C12N2330/10; C12N2770/00; C12N2770/00011; C12N2770/24011; C12N2770/24211

Claims Analysis

Total Claims: 19
Claim 1
Independent Claim 61 words
A method of reducing the amount of Hepatitis C virus replication in a target cell, said method comprising: introducing into a target cell infected with Hepatitis C virus, a miRNA inhibitory agent targeted to miR-122 in an amount sufficient to decrease the activity of miR-122 in said target cell, wherein said miRNA inhibitory agent comprises an antisense oligonucleotide complementary to miR-122.
Claim 2
Independent Claim 61 words
A method of reducing the amount of Hepatitis C virus replication in a target cell, said method comprising: introducing into a target cell infected with Hepatitis C virus, a miRNA inhibitory agent targeted to miR-122 in an amount sufficient to decrease the activity of miR-122 in said target cell, wherein said miRNA inhibitory agent comprises an antisense oligonucleotide complementary to miR-122.
Claim 3
Dependent Claim 14 words
The method according to claim 1 , wherein said target cell is in vitro.
Claim 4
Dependent Claim 14 words
The method according to claim 1 , wherein said target cell is in vivo.
Claim 5
Dependent Claim 23 words
The method according to claim 3 , wherein said method comprises administering the miRNA inhibitory agent to a subject comprising said target cell.
Claim 6
Dependent Claim 20 words
The method according to claim 4 , wherein said method comprises treating said subject for an HCV mediated disease condition.
Claim 7
Independent Claim 66 words
A method of reducing the amount of Hepatitis C virus replication in a target cell, said method comprising: introducing into a target cell infected with Hepatitis C virus, a miRNA inhibitory agent targeted to miR-122 in an amount sufficient to decrease the activity of miR-122 in said target cell, wherein said miRNA inhibitory agent is an antisense oligonucleotide comprising a nucleotide sequence of SEQ ID NO:18.
Claim 8
Independent Claim 66 words
A method of reducing the amount of Hepatitis C virus replication in a target cell, said method comprising: introducing into a target cell infected with Hepatitis C virus, a miRNA inhibitory agent targeted to miR-122 in an amount sufficient to decrease the activity of miR-122 in said target cell, wherein said miRNA inhibitory agent is an antisense oligonucleotide comprising a nucleotide sequence of SEQ ID NO:18.
Claim 9
Dependent Claim 14 words
The method according to claim 6 , wherein said target cell is in vitro.
Claim 10
Dependent Claim 14 words
The method according to claim 6 , wherein said target cell is in vivo.
Claim 11
Dependent Claim 23 words
The method according to claim 8 , wherein said method comprises administering the miRNA inhibitory agent to a subject comprising said target cell.
Claim 12
Dependent Claim 20 words
The method according to claim 8 , wherein said method comprises treating said subject for an HCV mediated disease condition.
Claim 13
Dependent Claim 19 words
The method according to claim 6 , wherein the antisense oligonucleotide comprises a nucleotide sequence of SEQ ID NO:15.
Claim 14
Dependent Claim 19 words
The method according to claim 1 , wherein the antisense oligonucleotide comprises a nucleotide sequence of SEQ ID NO:18.
Claim 15
Dependent Claim 19 words
The method according to claim 1 , wherein the antisense oligonucleotide comprises a nucleotide sequence of SEQ ID NO:15.
Claim 16
Independent Claim 63 words
A method of reducing the amount of Hepatitis C virus replication in a target cell in vitro, said method comprising: introducing into a target cell infected with Hepatitis C virus, a miRNA inhibitory agent targeted to miR-122 in an amount sufficient to decrease the activity of miR-122 in said target cell, wherein said miRNA inhibitory agent is an antisense oligonucleotide complementary to miR-122.
Claim 17
Independent Claim 63 words
A method of reducing the amount of Hepatitis C virus replication in a target cell in vitro, said method comprising: introducing into a target cell infected with Hepatitis C virus, a miRNA inhibitory agent targeted to miR-122 in an amount sufficient to decrease the activity of miR-122 in said target cell, wherein said miRNA inhibitory agent is an antisense oligonucleotide complementary to miR-122.
Claim 18
Dependent Claim 19 words
The method according to claim 14 , wherein the antisense oligonucleotide comprises a nucleotide sequence of SEQ ID NO:18.
Claim 19
Dependent Claim 19 words
The method according to claim 14 , wherein the antisense oligonucleotide comprises a nucleotide sequence of SEQ ID NO:15.

References Cited (Backward Citations)

US20050059005A1 Cited
US20040175732A1 Cited
WO2004076622A2 Cited
US20050227256A1 Cited

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