Coronavirus IRNA compositions and methods of use thereof
The present invention relates to RNAi agents, e.g., dsRNA agents, targeting the coronavirus genome. The invention also relates to methods of using such RNAi agents to inhibit expression of a coronavirus genome and to methods of treating or preventing a coronavirus-associated disease in a subject.
1. A double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of a coronavirus genome in a cell, or a salt thereof,
wherein the dsRNA agent, or a salt thereof, comprises a sense strand and an antisense strand forming a double stranded region,
wherein the antisense strand comprises a nucleotide sequence differing by no more than three bases from any one of the antisense strand nucleotide sequences selected from the group consisting of
(a) 5′-CCGGGUUUGACAGUUUGAAAAGC-3′ of SEQ ID NO: 586;
(b) 5′-GAUUAAAGAUUGCUAUGUGAGAU-3′ of SEQ ID NO: 719; and
(c) 5′-UCGGGUUUGACAGUUUGAAAAGC-3′ of SEQ ID NO: 1852.
2. An isolated cell containing the dsRNA agent, or a salt thereof, of claim 1 .
3. A pharmaceutical composition for inhibiting expression of a coronavirus genome, comprising the dsRNA agent, or a salt thereof, of claim 1 .
4. The dsRNA agent, or a salt thereof, of claim 1 , wherein the sense strand is conjugated to one or more lipophilic moieties.
5. The dsRNA agent, or a salt thereof, of claim 4 , wherein the one or more lipophilic moieties is selected from the group consisting of lipid, cholesterol, retinoic acid, cholic acid, adamantane acetic acid, 1-pyrene butyric acid, dihydrotestosterone, 1,3-bis-O (hexadecyl) glycerol, geranyloxyhexyanol, hexadecylglycerol, borneol, menthol, 1,3-propanediol, heptadecyl group, palmitic acid, myristic acid, 03-(oleoyl) lithocholic acid, 03-(oleoyl) cholenic acid, dimethoxytrityl, or phenoxazine.
6. The dsRNA agent, or a salt thereof, of claim 5 , wherein the one or more lipophilic moieties is an aliphatic, alicyclic, or polyalicyclic compound.
7. The dsRNA agent, or a salt thereof, of claim 6 , wherein the one or more lipophilic moieties contains a saturated or unsaturated C4-C30 hydrocarbon chain.
8. The dsRNA agent, or a salt thereof, of claim 7 , wherein the one or more lipophilic moieties contains a saturated or unsaturated C16 hydrocarbon chain.
9. The dsRNA agent, or a salt thereof, of claim 8 , wherein the saturated or unsaturated C16 hydrocarbon chain is conjugated to position 6, counting from the 5′-end of the strand.
10. The dsRNA agent, or a salt thereof, of claim 9 , wherein the saturated or unsaturated C16 hydrocarbon chain is conjugated to a nucleobase, a sugar moiety, or an internucleoside linkage.
11. The dsRNA agent, or a salt thereof, of claim 10 , wherein the saturated or unsaturated C16 hydrocarbon chain comprises a 2′-O-hexadecyl-adenosine-3′-phosphate nucleotide.
12. The dsRNA agent, or a salt thereof, of claim 1 , wherein all of the nucleotides of sense strand and all of the nucleotides of the antisense strand comprise a nucleotide modification.
13. The dsRNA agent, or a salt thereof, of claim 1 , wherein the dsRNA agent, or a salt thereof, further comprises at least one phosphorothioate internucleotide linkage.
14. The dsRNA agent, or a salt thereof, of claim 1 , wherein the dsRNA agent, or a salt thereof, further comprises a phosphate or phosphate mimic at the 5′-end of the antisense strand.
15. The dsRNA agent, or a salt thereof, of claim 14 , wherein the phosphate mimic is a 5′-vinyl phosphonate (VP).
16. The dsRNA agent, or a salt thereof, of claim 1 , wherein at least one strand comprises a 3′ overhang of at least 1 nucleotide.
17. The dsRNA agent, or a salt thereof, of claim 1 , wherein the nucleotide sequence of the sense strand differs by no more than 3 bases from the nucleotide sequence 5′-UUUUCAAACUGUCAAACCCGG-3′ of SEQ ID NO: 231 and the nucleotide sequence of the antisense strand differs by no more than 3 bases from the nucleotide sequence 5′-CCGGGUUUGACAGUUUGAAAAGC-3′ of SEQ ID NO: 586.
18. The dsRNA agent, or a salt thereof, of claim 1 , wherein the nucleotide sequence of the sense strand differs by no more than 3 bases from the nucleotide sequence 5′-CUCACAUAGCAAUCUUUAAUC-3′ of SEQ ID NO: 364 and the nucleotide sequence of the antisense strand differs by no more than 3 bases from the nucleotide sequence 5′-GAUUAAAGAUUGCUAUGUGAGAU-3′ of SEQ ID NO: 719.
19. The dsRNA agent, or a salt thereof, of claim 1 , wherein the nucleotide sequence of the sense strand differs by no more than 3 bases from the nucleotide sequence 5′-UUUUCAAACUGUCAAACCCGA-3′ of SEQ ID NO: 1812 and the nucleotide sequence of the antisense strand differs by no more than 3 bases from the nucleotide sequence 5′-UCGGGUUUGACAGUUUGAAAAGC-3′ SEQ ID NO: 1852.
20. The dsRNA agent, or a salt thereof, of claim 1 , wherein the sense strand comprises the nucleotide sequence 5′-ususuuc(Ahd)AfaCfUfGfucaaacccsgsa-3′ of SEQ ID NO:941 and the antisense strand comprises the nucleotide sequence 5′-VPusCfsgggUfuugacagUfuUfgaaaasgsc-3′ of SEQ ID NO:1296,
wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; s is a phosphorothioate linkage; (Ahd) is 2′-O-hexadecyl-adenosine-3′-phosphate; and VP is Vinyl-phosphonate.
21. The dsRNA agent, or a salt thereof, of claim 1 , wherein the sense strand comprises the nucleotide sequence 5′-csuscac(Ahd)UfaGfCfAfaucuuuaasusa-3′ of SEQ ID NO: 1074 and the antisense strand comprises the nucleotide sequence 5′-VPusAfsuuaAfagauugcUfaUfgugagsasu-3′ of SEQ ID NO:1429,
wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; s is a phosphorothioate linkage; (Ahd) is 2′-O-hexadecyl-adenosine-3′-phosphate; and VP is Vinyl-phosphonate.
22. The dsRNA agent, or a salt thereof, of claim 1 , wherein the sense strand comprises the nucleotide sequence 5′-ususuu(Chd)aAfaCfUfGfucaaacccsgsa-3′ of SEQ ID NO: 1895 and the antisense strand comprises the nucleotide sequence 5′-VPusCfsgggUfuugacagUfuUfgaaaasgsc-3′ of SEQ ID NO:1296
wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; s is a phosphorothioate linkage; (Chd) is 2′-O-hexadecyl-cytidine-3′-phosphate; and VP is Vinyl-phosphonate.