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Flavivirus Vaccine Polynucleotides Inducing Protective CD8+ T Cell Immunity

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Summary

USPTO published patent application US20260097108A1 by inventors Charneau et al. disclosing recombinant polynucleotides encoding non-structural antigens from Dengue virus (DENV), Zika virus (ZIKV), and Yellow Fever virus (YFV) designed to elicit protective CD8+ T-cell immune responses. The application covers polyepitope fusion polypeptides and lentiviral vectors for flavivirus vaccine development.

What changed

USPTO published patent application US20260097108A1 disclosing polynucleotides and lentiviral vectors expressing non-structural flavivirus antigens from DENV, ZIKV, and YFV. The claimed invention utilizes MHC class I T-cell epitopes in fusion polypeptides to induce protective CD8+ T-cell immunity.

Pharmaceutical and biotechnology companies developing flavivirus vaccines should monitor this application for potential licensing opportunities or to assess freedom-to-operate. The broad claim scope covering multiple flaviviruses and polyepitope approaches may overlap with competing vaccine programs.

What to do next

  1. Monitor for patent prosecution updates
  2. Review claims for potential freedom-to-operate concerns if developing flavivirus vaccines

Archived snapshot

Apr 9, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

POLYNUCLEOTIDES AND LENTIVIRAL VECTORS EXPRESSING NON-STRUCTURAL ANTIGENS OF A FLAVIVIRUS SELECTED FROM THE GROUP OF DENV, ZIKV AND YFV, INDUCING PROTECTIVE CD8+ T-CELL IMMUNITY IN A HOST

Application US20260097108A1 Kind: A1 Apr 09, 2026

Inventors

Pierre CHARNEAU, Kirill NEMIROV, Pierre AUTHIE, Philippe SOUQUE, Amandine NOIRAT, Fanny MONCOQ

Abstract

The invention relates to recombinant polynucleotides encoding at least a recombinant polynucleotide expressing at least a first fusion polypeptide that comprises MHC class I T-cell epitopes suitable to elicit a T cell immune response in a host in need thereof, wherein the MHC class I T-cell epitopes originate from a plurality of antigens wherein the antigens comprise at least non-structural antigens and are from at least one flavivirus selected from the group of 10 Dengue virus (DENV), ZIKA virus (ZIKV) and Yellow Fever virus (YFV). The invention also relates to the polypeptides comprising polyepitopes of said antigens encoded by the recombinant polynucleotides.

CPC Classifications

A61K 39/12 C07K 14/70539 C12N 5/0602 C12N 7/04 C12N 15/625 C12N 15/86 A61K 2039/53 A61K 2039/70 C07K 2319/00 C12N 2740/15043 C12N 2770/24134

Filing Date

2023-10-20

Application No.

19120869

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Last updated

Classification

Agency
USPTO
Published
April 9th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260097108A1

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers Healthcare providers
Industry sector
3254 Pharmaceutical Manufacturing 3254.1 Biotechnology
Activity scope
Patent application filing Vaccine research Gene therapy vector development
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare Biotechnology

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