Attenuating viral mutations in protein genes

Patent metadata

Field	Value
Publication number	US-12318439-B2
Application number	US-202217737991-A
Country	US
Kind code	B2
Filing date	May 5, 2022
Priority date	May 9, 2021
Publication date	Jun 3, 2025
Grant date	Jun 3, 2025

Abstract

Embodiments relate to attenuated flaviviruses for use in vaccines and immunogenic compositions. Embodiments include methods for treating or preventing one or more conditions, for example flavivirus infection, using an attenuated flavivirus. In some embodiments, the provided methods and compositions involve one or more attenuated flaviviruses that are capable of inducing a protective immune response.

First claim

The invention claimed is:

1. An attenuated flavivirus genome comprising a NS4B gene segment encoding a mutant NS4B protein having an amino acid substitution analogous to an alanine or glycine substitution at proline 54 of the West Nile Virus (WNV) NS4B protein, SEQ ID NO: 19.

2. The attenuated flavivirus genome of claim 1 , comprising one or more mutations in the gene segment encoding non-structural protein 1 (NS1), analogous to amino acids 792 to 1143 of SEQ ID NO: 2, the one or more mutations resulting in disruption of one or more glycosylation sites of the NS1 protein.

3. The attenuated flavivirus genome of claim 2 , wherein the one or more mutations in the glycosylation sites of the NS1 protein is a substitution of one or more of wild-type amino acids asparagine 130, asparagine 131, or threonine 132 of NS1.

4. The attenuated flavivirus genome of claim 3 , wherein the substitution of wild-type amino acids asparagine 130, asparagine 131, or asparagine 130 and asparagine 131 is a substitution of an asparagine residue with a polar amino acid.

5. The attenuated flavivirus genome of claim 4 , wherein the polar amino acid is a glutamine residue.

6. The attenuated flavivirus genome of claim 3 , wherein the substitution of amino acid threonine 132 is a substitution of the threonine residue with a nonpolar amino acid.

7. The attenuated flavivirus genome of claim 6 , wherein the nonpolar amino acid is an alanine residue.

8. The attenuated flavivirus genome of claim 3 , wherein the one or more mutations corresponding to one or more glycosylation sites of NS1 of the flavivirus further comprise a substitution of wild-type amino acid 175 of NS1, a substitution of wild-type amino acid 207 of NS1, or a substitution of wild-type amino acid 175 and amino acid 207 of NS1.

9. The attenuated flavivirus genome of claim 8 , wherein the substitution of wild-type amino acid asparagine 175, wild-type amino acid asparagine 207, or wild-type amino acid asparagine 175 and wild-type amino acid asparagine 207 is a substitution of an asparagine residue with a nonpolar amino acid.

10. The attenuated flavivirus genome of claim 9 , wherein the nonpolar amino acid is an alanine residue.

11. A nucleic acid construct encoding the genome of the attenuated flavivirus of claim 1 .

12. The nucleic acid construct of claim 11 , wherein the flavivirus is selected from the group consisting of West Nile virus, Japanese encephalitis virus, St. Louis encephalitis virus, tickborne encephalitis virus, Zika virus, dengue fever virus, and yellow fever virus (YFV).

13. The nucleic acid construct of claim 11 , wherein the flavivirus is yellow fever virus (YFV).

14. The nucleic acid construct of claim 11 , wherein the nucleic acid encoding the genome of the attenuated flavivirus further comprises one or more mutations corresponding to one or more glycosylation sites of non-structural protein 1 (NS1) of the flavivirus.

15. An immunogenic composition comprising the attenuated flavivirus encoded by claim 1 and a pharmaceutically acceptable carrier or diluent.

16. A method of inducing an immune response in a subject comprising administering an effective amount of the composition of claim 15 to the subject.

17. The method of claim 16 , wherein the subject is a non-human primate, a human, a horse, or a bird.

18. A vaccine composition comprising the attenuated flavivirus genome of claim 1 or an attenuated flavivirus encoded by the attenuated genome of claim 1 and a pharmaceutically acceptable carrier or diluent.

19. The attenuated flavivirus genome of claim 1 , wherein the flavivirus is selected from the group consisting of West Nile virus, Japanese encephalitis virus, St. Louis encephalitis virus, tickborne encephalitis virus, Zika virus, dengue fever virus, and yellow fever virus (YFV).

Assignees

• Univ Texas

Inventors

• Kaiser Jaclyn
• Wang Tian
• Barrett Alan
• Carpio Kassandra

Classifications

• A61K39/00

  Medicinal preparations containing antigens or antibodies (materials for immunoassay G01N33/53) · CPC title

• C12N7/00

  Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof (preparing medicinal viral antigen or antibody compositions, e.g. virus vaccines, A61K39/00) · CPC title

• A61K2039/5254

  avirulent or attenuated · CPC title

• A61P31/14 Primary

  for RNA viruses · CPC title

• C12N2770/24134

  Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein · CPC title