Low-Dose Multivalent Vaccine Composition for Broad Variant Protection

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Solution Overview

Problem

Existing vaccines often require a minimum dose of antigen components to elicit an optimal immune response, and there is a need for compositions that can effectively prevent pathogens from diverse phylogenetic families like influenza and HIV.

Innovation Solution

A vaccine composition comprising a plurality of RNAs and viral-like particles that encode or display six or more homologous distinct antigen components with less than 98% sequence identity, present in specific amounts ranging from 1 ng to 5 micrograms, to induce an immune response.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If multiple homologous antigen components are included in a vaccine composition, then broad protection against diverse pathogens is achieved, but the complexity of the composition increases

Engineering Contradiction:
Improvebroad protectionVSAvoidcomposition complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The vaccine composition is segmented into multiple discrete antigen components (six or more homologous distinct antigen components) that can be individually encoded by separate RNAs or displayed on separate viral-like particles. This segmentation allows each component to target specific pathogen variants while maintaining overall compositional manageability through modular design

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The vaccine composition achieves multi-functionality by incorporating multiple homologous distinct antigen components that collectively provide broad protection against diverse pathogens from the same phylogenetic family. Each antigen component contributes to universal coverage while maintaining specificity for different variants

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

2Device complexity

If low doses of antigen components are used, then the vaccine composition simplicity is improved, but the immune response effectiveness may be compromised

Engineering Contradiction:
Improvecomposition simplicityVSAvoidimmune response effectiveness
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

Multiple antigen components are merged into a single vaccine composition where each component is present at low individual doses (1 ng to 5 micrograms). The combined effect of multiple low-dose components achieves broad immune coverage that would be difficult to attain with high doses of single components, thereby maintaining simplicity while ensuring effectiveness

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The dose parameters for each antigen component are optimized to fall within the range of 1 ng to 5 micrograms. This parameter optimization ensures that each component elicits sufficient immune response at low doses, while the collective effect of multiple components provides comprehensive protection without requiring high individual doses

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS20260027196A1Low dose vaccine compositions
Publication Date: 2026.01.29 CENTIVAX INC
  • US20260027196A1 patent drawing
  • US20260027196A1 patent drawing
  • US20260027196A1 patent drawing

AI summary

The present disclosure provides a vaccine composition comprising six or more homologous distinct antigen components. Any two of the six or more homologous distinct antigen components may share less than 98% or 95% sequence identity. The homologous distinct antigen components may comprise proteins. An amount of a protein in a dose of said human adult vaccine composition may be about 600 nanograms (ng) to about 3 micrograms (μg). The homologous distinct antigen components may comprise a plurality of RNA. An amount of an RNA of said plurality of RNA in a dose of said vaccine composition may be about 1 ng to about 5 μg per dose. The homologous distinct antigen components may comprise a plurality of proteins displayed on heterologous viral-like particles (VLPs). An amount of a protein displayed on a heterologous VLP of the plurality of proteins displayed on heterologous VLPs in a dose of the vaccine composition may be about 1 ng to about 5 μg per dose.