Compositions comprising immunostimulatory siRNA molecules and DLinDMA or DLenDMA
View Patent ↗The present invention provides siRNA molecules and methods of using such siRNA molecules to modulate an immune response and to silence expression of a target gene.
1. A nucleic acid-lipid particle comprising:
(a) a modified siRNA comprising a double-stranded sequence of about 15 to about 30 nucleotides in length, said sequence comprising a non-immunostimulatory mismatch motif relative to an unmodified siRNA sequence that is capable of silencing expression of a target sequence, wherein the mismatch motif consists of a 5′-XX′-3′ dinucleotide corresponding to a 5′-GU-3′ dinucleotide in the sense or antisense strand of the unmodified siRNA sequence, wherein X and X′ are independently selected from the group consisting of A, U, C, and G, with the proviso that if X is G, X′ is not U and if X′ is U, X is not G,
wherein the modified siRNA is less immunogenic than the unmodified siRNA sequence, and
wherein the modified siRNA is capable of silencing expression of the target sequence;
(b) a cationic lipid, wherein said cationic lipid is selected from the group consisting of 1,2-DiLinoleyloxy-N,N-dimethylaminopropane (DLinDMA), 1,2-Dilinolenyloxy-N,N-dimethylaminopropane (DLenDMA), and a mixture thereof;
(c) a non-cationic lipid; and
(d) a conjugated lipid that inhibits aggregation of particles.
2. The nucleic acid-lipid particle in accordance with claim 1 , wherein the modified siRNA has reduced toxicity relative to an siRNA that is not in a nucleic acid-lipid particle.
3. The nucleic acid-lipid particle in accordance with claim 1 , wherein said cationic lipid is DLinDMA.
4. The nucleic acid-lipid particle in accordance with claim 1 , wherein said non-cationic lipid is a member selected from the group consisting of distearoylphosphatidylcholine (DSPC), dioleoylphosphatidylcholine (DOPC), dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylglycerol (DOPG), dipalmitoylphosphatidylglycerol (DPPG), dioleoyl-phosphatidylethanolamine (DOPE), palmitoyloleoylphosphatidylcholine (POPC), palmitoyloleoyl-phosphatidylethanolamine (POPE), dioleoyl- phosphatidylethanolamine 4-(N-maleimidomethyl)-cyclohexane-1-carboxylate (DOPE-mal), dipalmitoyl phosphatidyl ethanolamine (DPPE), dimyristoylphosphoethanolamine (DMPE), distearoyl-phosphatidyl-ethanolamine (DSPE), 16O-monomethyl PE, 16-O-dimethyl PE, 18-1-trans PE, 1-stearoyl-2-oleoyl-phosphatidyethanolamine (SOPE), cholesterol, and a mixture thereof.
5. The nucleic acid-lipid particle in accordance with claim 1 , wherein said non-cationic lipid is DSPC.
6. The nucleic acid-lipid particle in accordance with claim 1 , wherein the conjugated lipid that inhibits aggregation of particles comprises a polyethyleneglycol (PEG)-lipid and the PEG-lipid is member selected from the group consisting of a PEG-diacylglycerol, a PEG dialkyloxypropyl, a PEG-phospholipid, a PEG-ceramide, and a mixture thereof.
7. The nucleic acid-lipid particle in accordance with claim 1 , wherein the conjugated lipid that inhibits aggregation of particles comprises a PEG-dialkyloxypropyl (DAA) conjugate.
8. The nucleic acid-lipid particle in accordance with claim 7 , wherein the PEG-DAA conjugate is a member selected from the group consisting of a PEG-dilauryloxypropyl (C 12 ), a PEG-dimyristyloxypropyl (C 14 ), a PEG-dipalmityloxypropyl (C 16 ), and a PEG-distearyloxypropyl (C 18 ).
9. The nucleic acid-lipid particle in accordance with claim 7 , wherein the PEG-DAA conjugate is a PEG-dimyristyloxypropyl (C 14 ).
10. The nucleic acid-lipid particle in accordance with claim 1 , wherein said cationic lipid comprises from about 15% to about 35% of the total lipid present in said particle.
11. The nucleic acid-lipid particle in accordance with claim 1 , wherein said non-cationic lipid comprises from about 15% to about 25% of the total lipid present in said particle.
12. The nucleic acid-lipid particle in accordance with claim 7 , wherein said PEG-DAA conjugate comprises from 1% to about 10% of the total lipid present in said particle.
13. The nucleic acid-lipid particle in accordance with claim 7 , wherein said PEG-DAA conjugate comprises about 2% of the total lipid present in said particle.
14. The nucleic acid-lipid particle in accordance with claim 1 , further comprising cholesterol.
15. The nucleic acid-lipid particle in accordance with claim 14 , wherein the cholesterol comprises from about 40% to about 60% of the total lipid present in said particle.
16. The nucleic acid-lipid particle in accordance with claim 1 , wherein the modified siRNA is fully encapsulated in said nucleic acid-lipid particle.
17. A composition comprising a nucleic acid-lipid particle in accordance with claim 1 and a carrier.
18. The nucleic acid-lipid particle in accordance with claim 1 , wherein said cationic lipid comprises from about 2% to about 60% of the total lipid present in said particle.
19. The nucleic acid-lipid particle in accordance with claim 1 , wherein said cationic lipid comprises from about 40% to about 50% of the total lipid present in said particle.
20. The nucleic acid-lipid particle in accordance with claim 1 , wherein said non-cationic lipid comprises from about 5% to about 90% of the total lipid present in said particle.
21. The nucleic acid-lipid particle in accordance with claim 1 , wherein said non-cationic lipid comprises from about 20% to about 85% of the total lipid present in said particle.
22. The nucleic acid-lipid particle in accordance with claim 14 , wherein the cholesterol comprises from about 20% to about 45% of the total lipid present in said particle.
23. The nucleic acid-lipid particle in accordance with claim 1 , wherein said particle has a median diameter of from about 50 nm to about 150 nm.
24. The nucleic acid-lipid particle in accordance with claim 1 , wherein said non-cationic lipid comprises a phospholipid and cholesterol, and wherein said conjugated lipid that inhibits aggregation of particles comprises a PEG-DAA conjugate.
25. The nucleic acid-lipid particle in accordance with claim 1 , wherein the modified siRNA further comprises a second non-immunostimulatory mismatch motif.
26. The nucleic acid-lipid particle in accordance with claim 1 , wherein the modified siRNA comprises a double-stranded sequence of about 19 to about 25 nucleotides in length.
27. The nucleic acid-lipid particle in accordance with claim 1 , wherein the modified siRNA comprises 3′ overhangs.
28. The nucleic acid-lipid particle in accordance with claim 1 , wherein said conjugated lipid that inhibits aggregation of particles comprises from about 1% to about 15% of the total lipid present in said particle.