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 device for generating an aerosol suspension of respirable particles comprising an siRNA, wherein the device is a nebulizer or a solid particulate therapeutic aerosol generator, and wherein the device comprises a composition comprising the siRNA consisting of a sense strand and an antisense strand, wherein the sense strand consists of the nucleotide sequence of SEQ ID NO:267 and the antisense strand consists of the nucleotide sequence of SEQ ID NO:268.
2. The device of claim 1 , wherein the device is a pressure driven jet nebulizer or an ultrasonic nebulizer.
3. The device of claim 2 , wherein the device is a pressure driven jet nebulizer.
4. The device of claim 1 , wherein the device is a solid particulate therapeutic aerosol generator.
5. The device of claim 4 , wherein the solid particulate therapeutic aerosol generator is an insufflator.
6. The device of claim 4 , wherein the solid particulate therapeutic aerosol generator is a metered dose inhalator.
7. The device of claim 1 , wherein the composition comprises a liquid carrier.
8. The device of claim 7 , wherein the liquid carrier comprises a hypertonic saline solution.
9. The device of claim 7 , wherein the liquid carrier comprises an isotonic solution.
10. The device of claim 7 , wherein the siRNA comprises up to 40% w/w of the composition.
11. The device of claim 7 , wherein the siRNA comprises less than 20% w/w of the composition.
12. The device of claim 1 , wherein the composition comprises a powder.
13. The device of claim 12 , wherein the powder is contained in capsules or cartridges.
14. The device of claim 12 , wherein the powder comprises a powder diluent.
15. The device of claim 1 , 3 , 6 , 9 , or 14 , wherein the composition comprises a therapeutic agent in addition to the siRNA.
16. The device of claim 1 , 3 , 6 , 9 , or 14 , wherein the composition comprises an siRNA stabilizing agent selected from the group consisting of a chelator and an RNAse inhibitor.
17. The device of claim 1 , 3 , 6 , 9 , or 14 , wherein the device generates respirable particles less than 5 microns in size.
18. A method of reducing the levels of a Respiratory Syncytical virus (RSV) protein, mRNA, or titer in lung or respiratory cells in a subject comprising the steps of using the device of claim 1 , 3 , 6 , 9 , or 14 on the subject.
19. A method of reducing the levels of a Respiratory Syncytical virus (RSV) protein, mRNA, or titer in lung or respiratory cells in a subject comprising the steps of using the device of claim 15 on the subject.
20. A method of reducing the levels of a Respiratory Syncytical virus (RSV) protein, mRNA, or titer in lung or respiratory cells in a subject comprising the steps of using the device of claim 16 on the subject.
21. The device of claim 1 , wherein the device is a pressure driven jet nebulizer, the composition comprises an isotonic solution, the siRNA comprises up to 40% w/w of the composition, and the device generates respirable particles less than 5 microns in size.
22. The device of claim 21 , wherein the composition comprises a therapeutic agent in addition to the siRNA.
23. The device of claim 21 , wherein the composition comprises an siRNA stabilizing agent selected from the group consisting of a chelator and an RNAse inhibitor.
24. A method of reducing the levels of a Respiratory Syncytical virus (RSV) protein, mRNA, or titer in lung or respiratory cells in a subject comprising the steps of using the device of claim 21 , 22 , or 23 on the subject.