Compositions and methods for modulating Tau expression
Disclosed are methods for modulating splicing of Tau mRNA in an animal with Tau antisense compounds. Also disclosed herein are methods for reducing expression of Tau mRNA and protein in an animal with Tau antisense compounds. Such compounds and methods are useful to treat, prevent, or ameliorate neurodegenerative diseases in an individual in need thereof. Examples of neurodegenerative diseases that can be treated, prevented, and ameliorated with the administration Tau antisense oligonucleotides include Alzheimer's Disease, Fronto-temporal Dementia (FTD), FTDP-17, Progressive Supranuclear Palsy, Chronic Traumatic Encephalopathy, Epilepsy, and Dravet's Syndrome.
1. A compound comprising a modified oligonucleotide consisting of 15 to 30 linked nucleosides and having a nucleobase sequence comprising a complementary region comprising at least 15 contiguous nucleobases complementary to an equal length portion of nucleobases 121708 to 122044 of SEQ ID NO.: 1, wherein each nucleoside of the modified oligonucleotide comprises a 2′-substituted sugar moiety and wherein each 2′-substituted sugar moiety is 2′-MOE.
2. The compound of claim 1 , wherein the modified oligonucleotide consists of 16 to 22 linked nucleosides.
3. The compound of claim 2 , wherein at least one nucleobase of the modified oligonucleotide is a modified nucleobase.
4. The compound of claim 3 , wherein the modified nucleobase is a 5-methylcytosine.
5. The compound of claim 4 , wherein the modified oligonucleotide comprises at least one modified internucleoside linkage.
6. The compound of claim 5 , wherein the modified internucleoside linkage is a phosphorothioate internucleoside linkage.
7. The compound of claim 4 , wherein each internucleoside linkage is a modified internucleoside linkage.
8. The compound of claim 7 , wherein each modified internucleoside linkage is a phosphorothioate internucleoside linkage.
9. A compound comprising a modified oligonucleotide consisting of 12 to 30 linked nucleosides and having a nucleobase sequence comprising a complementary region comprising at least 15 contiguous nucleobases complementary to an equal length portion of nucleobases 121873 to 121898 of SEQ ID NO: 1, wherein each nucleoside of the modified oligonucleotide comprises a modified sugar moiety.
10. The compound of claim 9 , wherein the nucleobase sequence of the modified oligonucleotide is at least 90% complementary to SEQ ID NO: 1.
11. The compound of claim 10 , wherein the modified oligonucleotide consists of 16 to 22 linked nucleosides.
12. The compound of claim 11 , wherein at least one nucleobase of the modified oligonucleotide is a modified nucleobase.
13. The compound of claim 12 , wherein the modified nucleobase is a 5-methylcytosine.
14. The compound of claim 13 , wherein the modified oligonucleotide comprises at least one modified internucleoside linkage.
15. The compound of claim 14 , wherein the modified internucleoside linkage is a phosphorothioate internucleoside linkage.
16. The compound of claim 13 , wherein each internucleoside linkage is a modified internucleoside linkage.
17. The compound of claim 16 , wherein each modified internucleoside linkage is a phosphorothioate internucleoside linkage.
18. The compound of claim 17 , wherein the modified sugar moiety is a 2′-substituted sugar moiety.
19. The compound of claim 18 , wherein the 2′-substituted sugar moiety is selected from among: 2′-OMe, 2′-F, and 2′-MOE.
20. The compound of claim 17 , wherein the modified sugar moiety is a bicyclic sugar moiety.
21. The compound of claim 20 , wherein the bicyclic sugar moiety is LNA or cEt.
22. The compound of claim 17 , wherein the modified sugar moiety is a sugar surrogate.
23. The compound of claim 22 , wherein the sugar surrogate is a morpholino.
24. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier or diluent.
25. A method of reducing or ameliorating one or more symptoms associated with a tau-associated disorder, comprising contacting a cell with a compound according to claim 1 .
26. The method of claim 25 , wherein the cell is in an animal.