RNAi modulation of RSV and therapeutic uses thereof
View Patent ↗The present invention is based on the in vivo demonstration that RSV can be inhibited through intranasal administration of iRNA agents as well as by parenteral administration of such agents. Further, it is shown that effective viral reduction can be achieved with more than one virus being treated concurrently. Based on these findings, the present invention provides general and specific compositions and methods that are useful in reducing RSV mRNA levels, RSV protein levels and viral titers in a subject, e.g., a mammal, such as a human. These findings can be applied to other respiratory viruses.
1. A formulation comprising an iRNA agent, wherein said iRNA agent consists of a sense strand with the nucleotide sequence of SEQ ID NO:267 and an antisense strand with the nucleotide sequence of SEQ ID NO:268, and wherein said formulation comprises at least one pharmaceutical carrier.
2. The formulation of claim 1 , further comprising a therapeutic agent in addition to said iRNA agent.
3. The formulation of claim 1 , wherein said therapeutic agent is a second iRNA agent.
4. The formulation of claim 3 , wherein said second iRNA agent is an anti-RSV iRNA agent.
5. The formulation of claim 1 , wherein said formulation is an aqueous formulation.
6. The formulation of claim 1 , wherein said formulation is at least partially crystalline, uniformly crystalline, or anhydrous.
7. The formulation of claim 1 , wherein said formulation comprises an iRNA stabilizing agent selected from the group consisting of a chelator and an RNAse inhibitor.
8. The formulation of claim 1 , wherein said at least one pharmaceutical carrier is selected from the group consisting of a polypeptide and an amino acid.
9. The formulation of claim 1 , wherein said at least one pharmaceutical carrier is a carbohydrate selected from the group consisting of a monosaccharide, disaccharide, or polysaccharide.
10. The formulation of claim 9 , wherein said carbohydrate is dextrose.
11. The formulation of claim 1 , wherein said at least one pharmaceutical carrier is PBS.
12. The formulation of claim 1 , wherein said formulation comprises from one to fifteen percent by weight of a physiologically acceptable salt.
13. The formulation of claim 1 , wherein said formulation is a respirable particle about 1 to 10 microns in size.
14. The formulation of claim 1 , wherein said formulation is a respirable particle about 10 to 500 microns in size.
15. The formulation of claim 1 , wherein said formulation is a powder.
16. The formulation of claim 1 , wherein said pharmaceutical carrier includes one or more agents selected from the group consisting of lactose and a surfactant.
17. The formulation of claim 1 , wherein said formulation comprises at least one unit dose of said iRNA agent, wherein said unit dose is between 1 and 150 mg.
18. A method of reducing the levels of a Respiratory Syncytical virus (RSV) protein, RSV mRNA or RSV titer in lung or respiratory cells in a subject comprising the steps of administering intranasally, or by direct adminstration to the lung, a formulation to said subject, wherein said formulation comprises an iRNA agent and at least one pharmaceutical carrier to said subject, wherein said iRNA agent consists of a sense strand with the nucleotide sequence of SEQ ID NO:267 and an antisense strand with the nucleotide sequence of SEQ ID NO:268.