HBV HDV Vaccine Composition DNA Prime Protein Boost

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current therapies for chronic hepatitis B and D infections are inadequate, with nucleoside analogues providing only lifelong suppression of viral replication and not eliminating the risk of cancer, and existing vaccines failing to establish prophylactic immunity against both infections.

Innovation Solution

The use of recombinant nucleic acids, DNA, RNA, proteins, polypeptides, or peptides comprising HBV and/or HDV antigens in a DNA prime/protein boost composition approach to induce immune responses, antibody production, and immunity against HBV and/or HDV infections.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If nucleoside analogues are used for HBV therapy, then viral replication is suppressed, but the risk of cancer is not eliminated and lifelong treatment is required

Engineering Contradiction:
Improveviral replication suppressionVSAvoidtreatment duration
Core Design Contradiction:
ReliabilityVSDuration of action of moving object

Solution Approach 1:

The vaccine is administered before HBV infection occurs, establishing prophylactic immunity in advance. This preliminary action prevents the need for lifelong suppressive therapy by creating protective antibodies and T-cell responses that block viral entry and replication before infection can establish

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The invention converts the harmful chronic infection state into a beneficial protective immune response. By using HBV antigens (PreS1, S, PreS2) as vaccine components, the harmful viral proteins are repurposed to stimulate protective immunity, transforming the pathogen's own structures into defensive tools

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

2Reliability

If existing vaccines are used, then some immune response is generated, but prophylactic immunity against both HBV and HDV is not established

Engineering Contradiction:
Improveimmune responseVSAvoidprotection coverage
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The invention merges HBV antigens (PreS1, S, PreS2) with HDV antigen (HDAg) into a single combined vaccine composition. This merging strategy simultaneously targets both viruses, establishing cross-protective immunity against HBV and HDV coinfection or superinfection through a single immunization regimen

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The vaccine composition is designed with multi-functionality to protect against multiple viral threats. The combination of HBV and HDV antigens creates a universal prophylactic that addresses both infections, which commonly occur together, providing broad-spectrum protection that exceeds single-virus vaccines

Inventive Principle:
Principle #6Universality (Multi-functionality)

3Reliability

If DNA-only or protein-only immunogenic compositions are used, then immune response is induced, but the response is insufficient compared to combined approaches

Engineering Contradiction:
Improveimmune response inductionVSAvoidantibody production
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The invention uses a composite immunogenic composition that combines DNA and protein components in a prime-boost strategy. The DNA prime induces initial antigen expression and immune cell activation, while the protein boost enhances antibody production and affinity maturation, creating a synergistic effect that produces superior immune responses compared to either component alone

Inventive Principle:
Principle #40Composite materials

Data Source

PatentUS20250197452A1Compositions and methods for treating and preventing hepatitis b and d
Publication Date: 2025.06.19 SVENSKA VACCINFABRIKEN PROD AB
  • US20250197452A1 patent drawing
  • US20250197452A1 patent drawing
  • US20250197452A1 patent drawing

AI summary

Disclosed herein are immunogenic compositions or product combinations of engineered hepatitis B and hepatitis D nucleic acids, genes, peptides, or proteins that can be used to elicit an immune response against a hepatitis B and/or hepatitis D infection. Also disclosed are methods of using the immunogenic compositions or product combinations in subjects to generate immune responses against HBV and/or HDV by administering the compositions or combinations, for example, with a nucleic acid prime and polypeptide boost approach.