US2015030573A1PendingUtilityA1

Bacterial mediated thf alpha gene silencing

Assignee: BETH ISRAEL HOSPITALPriority: Jun 15, 2007Filed: Oct 26, 2013Published: Jan 29, 2015
Est. expiryJun 15, 2027(~0.9 yrs left)· nominal 20-yr term from priority
A61P 37/08C12N 15/63C12N 2320/32C12N 15/111C12N 2320/30C12N 15/1136C12N 15/1131C12N 2310/14C12N 15/1135A61P 37/02C12N 2310/111C12N 15/113
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Claims

Abstract

Methods are described for the delivery of one or more small interfering RNAs (siRNAs) to a eukaryotic cell using a bacterium. Methods are also described for using this bacterium to regulate gene expression in eukaryotic cells using RNA interference, and methods for treating an inflammatory disease or disorder. The bacterium includes one or more siRNAs or one or more DNA molecules encoding one or more siRNAs. Vectors are also described for use with the bacteria of the invention for causing RNA interference in eukaryotic cells.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of delivering one or more siRNAs to mammalian cells, the method comprising introducing to said mammalian cells at least one invasive bacterium containing one or more siRNAs or one or more DNA molecules encoding one or more siRNAs, wherein the expressed siRNAs interfere with the mRNA of TNFα. 
     
     
         2 . An invasive bacterium comprising one or more siRNAs or one or more DNA molecules encoding one or more siRNAs, wherein the expressed siRNAs interfere with the mRNA of TNFα. 
     
     
         3 . A prokaryotic vector comprising at least one DNA molecule encoding one or more siRNAs and at least one RNA-polymerase III compatible promoter or at least one prokaryotic promoter, wherein the expressed siRNAs interfere with the mRNA of TNFα. 
     
     
         4 . The method of  claim 1 , wherein said invasive bacterium is a non-pathogenic or non-virulent bacterium. 
     
     
         5 . The method of  claim 1 , wherein said invasive bacterium is a therapeutic bacterium. 
     
     
         6 . The method of  claim 1 , wherein said mammalian cell is in vivo or in vitro. 
     
     
         7 . The method of  claim 1 , wherein said mammalian cell is selected from the group consisting of human, bovine, ovine, porcine, feline, buffalo, canine, goat, equine, donkey, deer, avian, bird, chicken and primate cells. 
     
     
         8 . The method of  claim 1 , wherein the mammalian cell is selected from the group consisting of a gastrointestinal epithelial cell and a macrophage. 
     
     
         9 . The method of  claim 1 , wherein said one or more DNA molecules encoding said one or more siRNAs are transcribed within the animal cell. 
     
     
         10 . The method of  claim 1 , wherein said one or more DNA molecules encoding said one or more siRNAs are transcribed within the bacterium. 
     
     
         11 . The method of  claim 1 , wherein said one or more DNA molecules encoding one or more siRNAs comprise a prokaryotic promoter. 
     
     
         12 . The method of  claim 11 , wherein said prokaryotic promoter is a T7 promoter. 
     
     
         13 . The method of  claim 1 , wherein said animal cells are infected with about 10 3  to 10 11  viable invasive bacteria. 
     
     
         14 . The method of  claim 1 , wherein said animal cells are infected at a multiplicity of infection ranging from about 0.1 to 10 6 . 
     
     
         15 . The method of  claim 1 , wherein the expressed siRNAs direct the multienzyme complex RNA-induced silencing complex of the cell to interact with the mRNA of TNFα. 
     
     
         16 . The method of  claim 1 , wherein expression of TNFα is decreased or inhibited. 
     
     
         17 . The invasive bacterium of  claim 2 , wherein said invasive bacterium is a non-pathogenic or non-virulent bacterium. 
     
     
         18 . The invasive bacterium of  claim 2 , wherein said invasive bacterium is a therapeutic bacterium. 
     
     
         19 . A composition comprising the bacterium of  claim 2  and a pharmaceutically acceptable carrier. 
     
     
         20 . A eukaryotic host cell comprising the bacterium of  claim 2 , and a pharmaceutically acceptable carrier.

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