Methods and compositions for the specific inhibition of alpha-1 antitrypsin by double-stranded RNA
This invention relates to compounds, compositions, and methods useful for reducing α-1 antitrypsin target RNA and protein levels via use of dsRNAs, e.g., Dicer substrate siRNA (DsiRNA) agents.
1. A double stranded nucleic acid (dsNA) for reducing expression of α-1 antitrypsin mRNA comprising first and second nucleic acid strands that form a duplex region of 21 base pairs, wherein said first and second nucleic acid strands are separate nucleic acid molecules, wherein each of said first and second nucleic acid strands has a nucleotide sequence consisting of 21 nucleotides, wherein each of said 21 nucleotides of each of said first and second nucleic acid strands is a modified nucleotide, wherein said modified nucleotide is a 2′-O-methyl nucleotide or a 2′-fluoro nucleotide, wherein each of said first and second nucleic acid strands comprises one or more phosphorothioate linkages, wherein a targeting ligand is attached to said first nucleic acid strand, wherein said first nucleic acid strand comprises one or more inverted abasic residues, wherein the nucleotide sequence of the first nucleic acid strand consists of SEQ ID NO: 1908, and wherein said second strand is 100% complementary to SEQ ID NO: 1908.
2. The dsNA of claim 1 , wherein each of said first and second nucleic acid strands comprises a 3′-terminus, and wherein said first nucleic acid strand comprises the phosphorothioate linkage at said 3′-terminus or said second nucleic acid strand comprises the phosphorothioate linkage at said 3′-terminus or each of said first and second nucleic acid strands comprises the phosphorothioate linkage at said a 3′-terminus.
3. The dsNA of claim 1 , further comprising a targeting ligand attached to said second nucleic acid strand or both first and second nucleic acid strands.
4. The dsNA of claim 1 , wherein said targeting ligand comprises a GalNAc moiety or a tri-antennary GalNAc moiety.
5. The dsNA of claim 1 , wherein said first nucleic acid strand comprises two or more inverted abasic residues.
6. The dsNA of claim 1 , wherein said second nucleic acid strand comprises one or more inverted abasic residues.
7. The dsNA of claim 5 , wherein said targeting ligand comprises a GalNAc moiety or a tri-antennary GalNAc moiety.
8. The dsNA of claim 1 , wherein said first and second nucleic acid strands each comprise one or more modification patterns.
9. The dsNA of claim 1 , wherein said first nucleic strand comprises three or more phosphorothioate linkages.
10. The dsNA of claim 1 , wherein said second nucleic strand comprises one or more phosphorothioate linkages.
11. The dsNA of claim 10 , wherein said second nucleic strand comprises three or more phosphorothioate linkages.
12. A double stranded nucleic acid (dsNA) for reducing expression of α-1 antitrypsin mRNA comprising first and second nucleic acid strands that form a duplex region of 21 base pairs, wherein said first and second nucleic acid strands are separate nucleic acid molecules, wherein each of said first and second nucleic acid strands has a nucleotide sequence consisting of 21 nucleotides, wherein each of said 21 nucleotides of each of said first and second nucleic acid strands is a modified nucleotide, wherein said modified nucleotide is a 2′-O-methyl nucleotide or a 2′-fluoro nucleotide, wherein each of said first and second nucleic acid strands comprises three or more phosphorothioate linkages, wherein a targeting ligand is attached to said first nucleic acid strand, wherein said first nucleic acid strand comprises two or more inverted abasic residues, wherein the nucleotide sequence of the first nucleic acid strand consists of SEQ ID NO: 1908, and wherein said second strand is 100% complementary to SEQ ID NO: 1908.
13. The dsNA of claim 12 , wherein said targeting ligand comprises a GalNAc moiety or a tri-antennary GalNAc moiety.
14. A pharmaceutical composition comprising the dsNA of claim 1 and a pharmaceutically acceptable carrier.
15. A pharmaceutical composition comprising the dsNA of claim 12 and a pharmaceutically acceptable carrier.
16. A method for reducing expression of a target α-1 antitrypsin mRNA in a human, the method comprising administering the dsNA of claim 1 to said human in an amount sufficient to reduce expression of said target α-1 antitrypsin mRNA in said human.
17. A method for reducing expression of a target α-1 antitrypsin mRNA in a human, the method comprising administering the dsNA of claim 12 to said human in an amount sufficient to reduce expression of said target α-1 antitrypsin mRNA in said human.