Therapeutics for glycogen storage disease type iii
This invention provides a range of translatable polynucleotide and oligomer molecules for expressing a human amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL), or a fragment thereof having AGL activity. The polynucleotide and oligomer molecules are expressible to provide the human AGL or a fragment thereof having AGL activity. The molecules can be used as active agents to express an active polypeptide or protein in cells or subjects. The agents can be used in methods for ameliorating, preventing, delaying onset, or treating a disease or condition associated with reduced activity of amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL) in a subject.
1 . A lipid nanoparticle (LNP) comprising: (a) a polynucleotide comprising a nucleobase sequence encoding a human amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (hAGL) of SEQ ID NO: 2, wherein the nucleobase sequence encoding hAGL is at least 97% identical to SEQ ID NO: 41, and wherein the polynucleotide comprises a 5′ cap, a 5′ untranslated region (5′ UTR), a 3′ untranslated region (3′ UTR), and a 3′ polyA tail; (b) a cationic lipid; (c) a neutral lipid; (d) a PEG-modified lipid; and (e) a sterol.
2 . The LNP of claim 1 , wherein at least one uridine residue in the polynucleotide is replaced with an N 1 -methylpseudouridine residue.
3 . The LNP of claim 1 , wherein all uridine residues in the polynucleotide are replaced with N 1 -methylpseudouridine residues.
4 . The LNP of claim 1 , wherein the 5′ UTR is derived from a tobacco etch virus (TEV).
5 . The LNP of claim 1 , wherein the 5′ UTR comprises SEQ ID NO: 3.
6 . The LNP of claim 1 , wherein the 3′ UTR is derived from a Xenopus beta globin.
7 . The LNP of claim 1 , wherein the 3′ UTR comprises SEQ ID NO: 5.
8 . The LNP of claim 1 , wherein the 3′ polyA tail is 60 to 220 adenosine nucleotides in length.
9 . The LNP of claim 1 , wherein the 3′ polyA tail is 100 adenosine nucleotides in length.
10 . The LNP of claim 1 , wherein the cationic lipid is selected from ATX-002, ATX-081, ATX-095, and ATX-126.
11 . The LNP of claim 1 , wherein the neutral lipid is 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC).
12 . The LNP of claim 1 , wherein the PEG-modified lipid is dimyristoylglycerol (DMG)-PEG-2K.
13 . The LNP of claim 1 , wherein the sterol is cholesterol.
14 . The LNP of claim 1 , wherein the lipids are provided in a molar ratio of 20-60% cationic lipid:5-25% neutral lipid:25-55% sterol:0.5-15% PEG-modified lipid.
15 . A method of treating glycogen storage disease type III (GSDIII), the method comprising administering to a subject a LNP of claim 1 .
16 . The method of claim 15 , wherein the administration is daily, weekly, biweekly, or monthly.
17 . The method of claim 15 , wherein the administration is intravenous or subcutaneous.
18 . The method of claim 15 , wherein the method comprises administration of a dose of the polynucleotide of 0.01 mg/kg to 10 mg/kg.
19 . The method of claim 15 , wherein the method comprises administration of a dose of the polynucleotide of at least 0.1 mg/kg.
20 . The method of claim 19 , wherein the administration is biweekly.