COMPLEMENT COMPONENT C3 iRNA COMPOSITIONS AND METHODS OF USE THEREOF
The invention relates to iRNA, e.g., double stranded ribonucleic acid (dsRNA), compositions targeting the complement factor C3 gene, and methods of using such iRNA, e.g., dsRNA, compositions to inhibit expression of a C3 gene and to treat subjects having a complement component C3-associated disease, e.g., paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), atypical hemolytic uremic syndrome (aHUS), neuromyelitis optica (NMO), multifocal motor neuropathy (MMN), myasthenia gravis (MG), and C3 glomerulonephritis.
1 . A double stranded ribonucleic acid (dsRNA) for inhibiting expression of complement component C3 in a cell,
a) wherein said dsRNA comprises a sense strand and an antisense strand,
wherein said sense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from the nucleotide sequence of SEQ ID NO:1, and said antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from the nucleotide sequence of SEQ ID NO:2,
wherein all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand comprise a nucleotide modification, and
wherein at least one strand comprises a ligand; or
b) wherein said dsRNA comprises a sense strand and an antisense strand,
wherein the antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the antisense sequences listed in any one of Tables 3, 4, 6, 7, and 9,
wherein all of the nucleotides of the sense strand and all of the nucleotides of the antisense strand comprise a nucleotide modification, and
wherein at least one strand comprises a ligand.
2 .- 5 . (canceled)
6 . The dsRNA agent of claim 1 , wherein at least one of the nucleotide modifications is selected from the group consisting of a deoxy-nucleotide modification, a 3′-terminal deoxy-thymine (dT) nucleotide modification, a 2′-O-methyl nucleotide modification, a 2′-fluoro nucleotide modification, a 2′-deoxy-nucleotide modification, a locked nucleotide modification, an unlocked nucleotide modification, a conformationally restricted nucleotide modification, a constrained ethyl nucleotide modification, an abasic nucleotide modification, a 2′-amino-nucleotide modification, a 2′-O-allyl-nucleotide modification, 2′-C-alkyl-nucleotide modification, 2′-hydroxly-nucleotide modification, a 2′-methoxyethyl nucleotide modification, a 2′-O-alkyl-nucleotide modification, a morpholino nucleotide modification, a phosphoramidate modification, a non-natural base comprising nucleotide modification, a tetrahydropyran nucleotide modification, a 1,5-anhydrohexitol nucleotide modification, a cyclohexenyl nucleotide modification, a nucleotide comprising a phosphorothioate group modification, a nucleotide comprising a methylphosphonate group modification, a nucleotide comprising a 5′-phosphate modification, and a nucleotide comprising a 5′-phosphate mimic modification.
7 . (canceled)
8 . The dsRNA agent of claim 1 , further comprising at least one phosphorothioate internucleotide linkage.
9 .- 14 . (canceled)
15 . The dsRNA agent of claim 1 , wherein each strand is independently no more than 30 nucleotides in length.
16 . (canceled)
17 . (canceled)
18 . The dsRNA agent of claim 1 , wherein at least one strand comprises a 3′ overhang of at least 1 nucleotide.
19 . (canceled)
20 . The dsRNA agent of claim 1 , further comprising a ligand.
21 . (canceled)
22 . The dsRNA agent of claim 1 , wherein the ligand is an N-acetylgalactosamine (GalNAc) derivative.
23 . The dsRNA agent of claim 22 , wherein the ligand is
24 . The dsRNA agent of claim 22 , wherein the dsRNA agent is conjugated to the ligand as shown in the following schematic
and, wherein X is O or S.
25 . The dsRNA agent of claim 24 , wherein the X is O.
26 . (canceled)
27 . A cell containing the dsRNA agent of claim 1 .
28 . (canceled)
29 . A pharmaceutical composition for inhibiting expression of a complement component C3 gene comprising the agent of claim 1 .
30 .- 34 . (canceled)
35 . A method of inhibiting complement component 3 (C3) expression in a cell, the method comprising contacting the cell with the agent of claim 1 , thereby inhibiting expression of the C3 gene in the cell.
36 . The method of claim 35 , wherein said cell is within a subject.
37 . The method of claim 36 , wherein the subject is a human.
38 .- 41 . (canceled)
42 . A method of treating a subject having a disorder that would benefit from reduction in complement component C3 (C3) expression, comprising administering to the subject a therapeutically effective amount of the agent of claim 1 , thereby treating said subject.
43 . (canceled)
44 . The method of claim 42 , wherein the disorder is a complement component C3-associated disease.
45 . The method of claim 44 , wherein the complement component C3-associated disease is selected from the group consisting of paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), atypical hemolytic uremic syndrome (aHUS), neuromyelitis optica (NMO), multifocal motor neuropathy (MMN), myasthenia gravis (MG), C3 glomerulonephritis, and systemic lupus erythmatosis.
46 . (canceled)
47 . The method of claim 42 , wherein the subject is human.
48 . (canceled)
49 . (canceled)
50 . The method of claim 42 , wherein the agent is administered to the subject subcutaneously.
51 .- 58 . (canceled)