Lipid Formulations for Delivery of Messenger RNA
The present invention provides, among other things, methods of delivering mRNA in vivo, including administering to a subject in need of delivery a composition comprising an mRNA encoding a protein, encapsulated within a liposome such that the administering of the composition results in the expression of the protein encoded by the mRNA in vivo, wherein the liposome comprises a cationic lipid of formula I-c: or a pharmaceutically acceptable salt thereof.
1 - 56 . (canceled)
57 . A method of delivery of messenger RNA (mRNA) in vivo, comprising administering to a subject in need of delivery a composition comprising an mRNA encapsulated within a liposome,
wherein administration of the composition results in the expression of a protein encoded by the mRNA in vivo;
wherein the liposome comprises a cationic lipid of formula I-g:
or a pharmaceutically acceptable salt thereof,
wherein R L is linear C 8-12 alkyl and the liposome further comprises a non-cationic lipid, a cholesterol-based lipid, and a PEG-modified lipid, and
wherein the mRNA has a length of or greater than about 0.5 kb.
58 . The method of claim 57 , wherein R L is linear —C 8 H 17 , —C 9 H 19 , —C 10 H 21 , —C 11 H 23 , or —C 12 H 25 .
59 . The method of claim 58 , wherein R L is linear —C 8 H 17 .
60 . The method of claim 57 , wherein the non-cationic lipid is selected from DSPC (1,2-distearoyl-sn-glycero-3-phosphocholine), DPPC (1,2-dipalmitoyl-sn-glycero-3-phosphocholine), DOPE (1,2-dioleyl-sn-glycero-3-phosphoethanolamine), DOPC (1,2-dioleyl-sn-glycero-3-phosphotidylcholine) DPPE (1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine), DMPE (1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine), and DOPG (1,2-dioleoyl-sn-glycero-3-phospho-(1′-rac-glycerol)).
61 . The method of claim 57 , wherein the cholesterol-based lipid is cholesterol or PEGylated cholesterol.
62 . The method of claim 57 , wherein the PEG-modified lipid comprises a poly(ethylene) glycol chain of up to 5 kDa in length covalently attached to a lipid with alkyl chain(s) of C 6 -C 20 length.
63 . The method of claim 59 , wherein the liposome comprises the cationic lipid, DOPE, cholesterol, and DMG-PEG2K.
64 . The method of claim 57 , wherein the cationic lipid constitutes about 30-50% of the liposome by molar ratio.
65 . The method of claim 64 , wherein the cationic lipid constitutes about 40% of the liposome by molar ratio.
66 . The method of claim 63 , wherein the ratio of cationic lipid: DOPE: cholesterol:DMG-PEG2K is approximately 40:30:20:10, 40:30:25:5, or 40:32:25:3 by molar ratio.
67 . The method of claim 57 , wherein the liposome has a size less than about 250 nm, 200 nm, 150 nm, 100 nm, 75 nm, or 50 nm.
68 . The method of claim 57 , wherein the composition is to be administered intravenously, intrathecally, or via pulmonary delivery.
69 . The method of claim 68 , wherein the pulmonary delivery is by aerosolization, inhalation, nebulization or instillation.
70 . The method of claim 57 , wherein the expression of the protein encoded by the mRNA is detectable in liver, kidney, heart, spleen, serum, brain, skeletal muscle, lymph nodes, skin, and cerebrospinal fluid.
71 . The method of claim 57 , wherein the expression of the protein encoded by the mRNA is detectable 3 hours, 6 hours, 12 hours, 24 hours, or 1 week after the administration.
72 . The method of claim 57 , wherein the mRNA has a length of or greater than about 1 kb, 1.5 kb, 2 kb, 2.5 kb, 3 kb, 3.5 kb, 4 kb, 4.5 kb, or 5 kb.
73 . The method of claim 57 , wherein the protein encoded by the mRNA is a cytosolic protein, a secreted protein, or an enzyme.
74 . The method of claim 57 , wherein the protein encoded by the mRNA is cystic fibrosis transmembrane conductance regulator (CFTR), argininosuccinate synthetase (ASS1), factor IX (FIX), survival of motor neuron 1 (SMN-1), or phenylalanine hydroxylase.
75 . The method of claim 57 , wherein the mRNA is administered at a dose ranging from about 0.1-2.0 mg/kg body weight.
76 . The method of claim 57 , wherein the mRNA is administered at a dose of or less than about 1.0 mg/kg, 0.5 mg/kg, or 0.3 mg/kg body weight.
77 . The method of claim 57 , wherein the mRNA is unmodified or comprises one or more modified nucleotides.
78 . The method of claim 77 , wherein the one or more modified nucleotides comprise pseudouridine, N-1-methyl-pseudouridine, 2-aminoadenosine, 2-thiothymidine, inosine, pyrrolo-pyrimidine, 3-methyl adenosine, 5-methylcytidine, C-5 propynyl-cytidine, C-5 propynyl-uridine, 2-aminoadenosine, C5-bromouridine, C5-fluorouridine, C5-iodouridine, C5-propynyl-uridine, C5-propynyl-cytidine, C5-methylcytidine, 2-aminoadenosine, 7-deazaadenosine, 7-deazaguanosine, 8-oxoadenosine, 8-oxoguanosine, 0(6)-methylguanine, and/or 2-thiocytidine.