Lipid nanoparticle vaccine adjuvants and antigen delivery systems
US-2016361411-A1 · Dec 15, 2016 · US
US12161709B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12161709-B2 |
| Application number | US-202117559190-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 22, 2021 |
| Priority date | Jan 11, 2017 |
| Publication date | Dec 10, 2024 |
| Grant date | Dec 10, 2024 |
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The present invention relates to compositions and methods for inducing an adaptive immune response against Zika virus (ZIKV) in a subject. In certain embodiments, the present invention provides a composition comprising a nucleoside-modified nucleic acid molecule encoding a ZIKV antigen, adjuvant, or a combination thereof. For example, in certain embodiments, the composition comprises a vaccine comprising a nucleoside-modified nucleic acid molecule encoding a ZIKV antigen, adjuvant, or a combination thereof.
Opening claim text (preview).
What is claimed is: 1. A composition for inducing an immune response against Zika virus (ZIKV) in a subject, the composition comprising at least one mRNA molecule encoding at least one ZIKV antigen, wherein the mRNA molecule comprises a sequence having at least 95% identity to the nucleotide sequence of SEQ ID NO: 1. 2. The composition of claim 1 , wherein the composition further comprises an adjuvant. 3. The composition of claim 1 , wherein the mRNA molecule further encodes at least one adjuvant. 4. The composition of claim 1 , further comprising a lipid nanoparticle (LNP). 5. The composition of claim 1 , wherein the at least one mRNA molecule is encapsulated within an LNP. 6. The composition of claim 1 , wherein the composition is a vaccine. 7. A method of inducing an adaptive immune response against Zika virus (ZIKV) in a subject comprising administering to the subject an effective amount of the composition of claim 1 . 8. The method of claim 7 , wherein the method further comprises administering to the subject an effective amount of an adjuvant. 9. The method of claim 7 , wherein the at least one mRNA molecule is encapsulated within an LNP. 10. The method of claim 7 , wherein the composition is a vaccine. 11. The method of claim 7 , wherein the composition is administered by a delivery route selected from the group consisting of intradermal, subcutaneous, inhalation, intranasal, and intramuscular. 12. The method of claim 7 , wherein the method comprises a single administration of the composition. 13. The method of claim 7 , wherein the method comprises multiple administrations of the composition. 14. A method of treating or preventing an infection, disease, or disorder associated with ZIKV in at least one selected from the group consisting of the subject and an unborn child of the subject, the method comprising administering to the subject the composition of claim 1 . 15. The method of claim 14 , wherein the at least one mRNA molecule comprises at least one modified nucleoside selected from the group consisting of pseudouridine, and 1-methyl-pseudouridine. 16. The method of claim 14 , wherein the composition further comprises an adjuvant. 17. The method of claim 14 , wherein the at least one mRNA molecule further encodes at least one adjuvant. 18. The method of claim 14 , further comprising a lipid nanoparticle (LNP). 19. The method of claim 14 , wherein the at least one mRNA is encapsulated within an LNP. 20. The method of claim 14 , wherein the composition is a vaccine. 21. The method of claim 14 , wherein the composition is administered by a delivery route selected from the group consisting of intradermal, subcutaneous, inhalation, intranasal, and intramuscular. 22. The method of claim 14 , wherein the method comprises a single administration of the composition. 23. The method of claim 14 , wherein the method comprises multiple administrations of the composition.
Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title
Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers · CPC title
Organic adjuvants · CPC title
characterised by the host/recipient, e.g. newborn with maternal antibodies · CPC title
characterised by the dose, timing or administration schedule · CPC title
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