Multi-Subtype Vaccine Molecules for Broad Influenza Protection

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Solution Overview

Problem

Conventional influenza vaccines are limited by their strain-specific nature, requiring time-consuming production and often failing to provide broad immunity against diverse influenza strains, especially due to antigenic drift and shifts.

Innovation Solution

A DNA vaccine formulation that targets hemagglutinin (HA) proteins from multiple influenza subtypes to major histocompatibility complex (MHC) class II molecules on antigen-presenting cells, inducing a mixture of HA proteins to enhance strain-specific and cross-protective antibody responses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If conventional influenza vaccines are used, then strain-specific immunity is achieved, but broad protection against diverse influenza strains is limited

Engineering Contradiction:
Improvebroad protection against diverse influenza strainsVSAvoidstrain-specific immunity effectiveness
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The vaccine composition combines multiple HA proteins from different influenza subtypes (H1, H3, H5, H7, H9, H10) into a single formulation, enabling the vaccine to provide both strain-specific immunity against individual subtypes and broad cross-protection against diverse influenza strains, including those not explicitly included in the mixture

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

Solution Approach 2:

The patent merges six different HA proteins into one vaccine composition that can be administered simultaneously, consolidating what would traditionally require multiple separate vaccines into a single multi-functional preparation that addresses both specific and broad protection needs

Inventive Principle:
Principle #5Merging (Combining)

2Productivity

If conventional vaccine production methods are used, then strain-specific vaccines are produced, but production time is substantial and production capacity is limited

Engineering Contradiction:
Improvevaccine production capacityVSAvoidproduction time
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The vaccine combines multiple HA proteins from different influenza subtypes into a single formulation that can be produced and administered together, eliminating the need for separate production lines and timing coordination for multiple individual vaccines, thereby substantially increasing production capacity and reducing time losses

Inventive Principle:
Principle #5Merging (Combining)

3Adaptability or versatility

If DNA vaccines encoding multiple HA proteins are used, then broad immunity is induced, but vaccine complexity increases

Engineering Contradiction:
Improvebroad immunity against multiple strainsVSAvoidvaccine composition complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The vaccine uses a universal approach by including HA proteins from six different influenza subtypes in a single composition, providing multi-functional protection that covers both current circulating strains and potential future variants, thereby achieving broad immunity through a standardized multi-component formulation rather than complex customized vaccines

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

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The vaccine mixture induces high titers of strain-specific antibodies and cross-reactive antibodies, providing protection against included and unrelated influenza strains, including unanticipated antigenic shifts.

Implementation Method 1

Each of the targeted DNA vaccines induced high titers of strain-specific anti-HA antibodies

Methodology Applied
Scientific EffectAntigen-antibody interaction:

Implementation Method 2

the vaccine mixture induced antibodies that cross-reacted with strains not included in the vaccine mixture

Methodology Applied
Scientific EffectImmune response:

Data Source

PatentUS12447205B2Vaccine molecules
Publication Date: 2025.10.21 UNIVERSITY OF OSLO
  • US12447205B2 patent drawing
  • US12447205B2 patent drawing
  • US12447205B2 patent drawing

AI summary

Provided herein is technology relating to vaccines and particularly, but not exclusively, to compositions, methods, and uses of a mixture of immunogenic vaccine molecules comprising components for targeting the dimeric vaccine molecules to antigen-presenting cells and components for eliciting an immunogenic response, wherein the components for eliciting an immunogenic response preferably comprise at least three variants of an immunogenic protein, such as variants of immunogenic proteins obtained from three or more different strains of a pathogenic organism.