US2004254133A1PendingUtilityA1

Antisense modulation of interferon gamma receptor 1 expression

Priority: Apr 26, 2001Filed: Apr 16, 2003Published: Dec 16, 2004
Est. expiryApr 26, 2021(expired)· nominal 20-yr term from priority
C12N 2310/341C12N 2310/3341A61K 38/00Y02P20/582C12N 2310/315C12N 2310/346C12N 15/1138C12N 2310/321
57
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Claims

Abstract

Antisense compounds, compositions and methods are provided for modulating the expression of Interferon gamma receptor 1. The compositions comprise antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding Interferon gamma receptor 1. Methods of using these compounds for modulation of Interferon gamma receptor 1 expression and for treatment of diseases associated with expression of Interferon gamma receptor 1 are provided.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A compound 8 to 50 nucleobases in length targeted to a nucleic acid molecule encoding Interferon gamma receptor 1, wherein said compound specifically hybridizes with and inhibits the expression of Interferon gamma receptor 1.  
     
     
         2 . The compound of  claim 1  which is an antisense oligonucleotide.  
     
     
         3 . The compound of  claim 2  wherein the antisense oligonucleotide has a sequence comprising SEQ ID NO: 11, 12, 13, 16, 17, 18, 22, 24, 25, 28, 29, 30, 41, 44, 45, 48, 53, 55, 57, 59, 61, 63, 65, 66, 67, 68, 70, 71, 73, 77, 79, 86 or 87.  
     
     
         4 . The compound of  claim 2  wherein the antisense oligonucleotide comprises at least one modified internucleoside linkage.  
     
     
         5 . The compound of  claim 4  wherein the modified internucleoside linkage is a phosphorothioate linkage.  
     
     
         6 . The compound of  claim 2  wherein the antisense oligonucleotide comprises at least one modified sugar moiety.  
     
     
         7 . The compound of  claim 6  wherein the modified sugar moiety is a 2′-O-methoxyethyl sugar moiety.  
     
     
         8 . The compound of  claim 2  wherein the antisense oligonucleotide comprises at least one modified nucleobase.  
     
     
         9 . The compound of  claim 8  wherein the modified nucleobase is a 5-methylcytosine.  
     
     
         10 . The compound of  claim 2  wherein the antisense oligonucleotide is a chimeric oligonucleotide.  
     
     
         11 . A compound 8 to 50 nucleobases in length which specifically hybridizes with at least an 8-nucleobase portion of an active site on a nucleic acid molecule encoding Interferon gamma receptor 1.  
     
     
         12 . A composition comprising the compound of  claim 1  and a pharmaceutically acceptable carrier or diluent.  
     
     
         13 . The composition of  claim 12  further comprising a colloidal dispersion system.  
     
     
         14 . The composition of  claim 12  wherein the compound is an antisense oligonucleotide.  
     
     
         15 . A method of inhibiting the expression of Interferon gamma receptor 1 in cells or tissues comprising contacting said cells or tissues with the compound of  claim 1  so that expression of Interferon gamma receptor 1 is inhibited.  
     
     
         16 . A method of treating an animal having a disease or condition associated with Interferon gamma receptor 1 comprising administering to said animal a therapeutically or prophylactically effective amount of the compound of  claim 1  so that expression of Interferon gamma receptor 1 is inhibited.  
     
     
         17 . The method of  claim 16  wherein the disease or condition is an autoimmune disorder.  
     
     
         18 . The method of  claim 17  wherein the autoimmune disorder is autoimmune thyroiditis, diabetes, multiple sclerosis, autoimmune arthritis, autoimmune insulinitis or Crohn's disease.  
     
     
         19 . The method of  claim 16  wherein the disease or condition is cancer.  
     
     
         20 . The method of  claim 16  wherein the disease or condition is caused by aberrant apoptosis.

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