US2022175906A1PendingUtilityA1
Zika virus rna vaccines
Est. expirySep 14, 2037(~11.1 yrs left)· nominal 20-yr term from priority
Y02A50/30A61K 39/12A61K 2039/575A61P 31/14A61K 48/005A61K 2039/55555A61K 2121/00A61K 2039/53A61K 2039/545C12N 2770/24134A61K 47/6931A61K 2039/525A61K 31/7088A61K 9/51A61K 2039/54
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Claims
Abstract
Provided herein, in some embodiments, are Zika virus RNA vaccines and methods of producing an antigen-specific immune response in a subject.
Claims
exact text as granted — not AI-modified1 . A method comprising administering to a subject a messenger ribonucleic acid (mRNA) comprising an open reading frame (ORF) encoding a Japanese encephalitis virus (JEV) signal peptide fused to a Zika virus (ZIKV) prME protein comprising a sequence having at least 90% identity to SEQ ID NO: 7, wherein the mRNA is in a composition comprising a lipid nanoparticle.
2 - 38 . (canceled)
39 . The method of claim 1 , wherein 20 μg-200 μg of the mRNA is administered to the subject.
40 . The method of claim 39 , wherein 20 μg-60 μg of the mRNA is administered to the subject.
41 . The method of claim 1 , wherein a first dose and a second dose of the mRNA is administered to the subject.
42 . The method of claim 1 , wherein the ZIKV prME protein comprises a sequence having at least 95% identity to SEQ ID NO: 7.
43 . The method of claim 42 , wherein the ZIKV prME protein comprises the sequence of SEQ ID NO: 7.
44 . The method of claim 1 , wherein the mRNA vaccine comprises at least one modified nucleotide.
45 . The method of claim 44 , wherein at least 80% of uracil nucleotides in the ORF of the mRNA have a 1-methyl-pseudouridine modification.
46 . The method of claim 45 , wherein 100% of uracil nucleotides in the ORF of the mRNA have a 1-methyl-pseudouridine modification.
47 . The method of claim 1 , wherein the lipid nanoparticle comprises 20-60 mol % ionizable cationic lipid, 5-25 mol % non-cationic lipid, 25-55 mol % sterol, and 0.5-15 mol % PEG-modified lipid.
48 . The method of claim 47 , wherein the ionizable cationic lipid comprises the following compound:
49 . A method comprising:
administering to a subject a first dose and a second dose of a messenger ribonucleic acid (mRNA) comprising an open reading frame (ORF) encoding a Japanese encephalitis virus (JEV) signal peptide fused to a Zika virus (ZIKV) prME protein comprising a sequence having at least 95% identity to SEQ ID NO: 7, wherein the mRNA is in a composition comprising a lipid nanoparticle.
50 . The method of claim 49 , wherein 20 μg-60 μg of the mRNA is administered to the subject.
51 . The method of claim 49 , wherein at least 80% of uracil nucleotides in the ORF of the mRNA have a 1-methyl-pseudouridine modification.
52 . The method of claim 51 , wherein 100% of uracil nucleotides in the ORF of mRNA have a 1-methyl-pseudouridine modification.
53 . The method of claim 49 , wherein the lipid nanoparticle comprises 20-60 mol % ionizable cationic lipid, 5-25 mol % non-cationic lipid, 25-55 mol % sterol, and 0.5-15 mol % PEG-modified lipid.
54 . The method of claim 53 , wherein the ionizable cationic lipid comprises the following compound:
55 . A method comprising:
administering to a subject a first dose and a second dose of a messenger ribonucleic acid (mRNA) comprising an open reading frame (ORF) encoding a Japanese encephalitis virus (JEV) signal peptide fused to a Zika virus (ZIKV) prME protein comprising a sequence having at least 95% identity to SEQ ID NO: 7, wherein 100% of uracil nucleotides in the ORF of mRNA have a 1-methyl-pseudouridine modification, and wherein the mRNA is in a composition comprising a lipid nanoparticle, and wherein 20 μg-60 μg of the mRNA is administered to the subject.
56 . The method of claim 55 , wherein the lipid nanoparticle comprises 20-60 mol % ionizable cationic lipid, 5-25 mol % non-cationic lipid, 25-55 mol % sterol, and 0.5-15 mol % PEG-modified lipid.
57 . The method of claim 56 , wherein the ionizable cationic lipid comprises the following compound:Join the waitlist — get patent alerts
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