Recombinant Influenza Virus M2 Mutation Microneedle Delivery

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Solution Overview

Problem

Current influenza vaccines face challenges in stability and effectiveness, particularly with live attenuated viruses that can revert to wild-type or non-wild-type sequences, and existing vaccines may not provide durable or cross-reactive immunity, and there is a need for improved methods to administer vaccines effectively.

Innovation Solution

A recombinant influenza virus with a mutation in the M gene that prevents expression of the M2 protein or results in a truncated protein, which is stable and non-pathogenic, is used in combination with a microneedle delivery device for intradermal administration to elicit a detectable immune response and provide protection against influenza.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If live attenuated influenza virus vaccines are used, then immune response effectiveness and durability are improved, but virus stability deteriorates due to potential reversion to wild-type sequences

Engineering Contradiction:
Improveimmune response effectivenessVSAvoidvirus genetic stability
Core Design Contradiction:
ReliabilityVSStability of the object's composition

Solution Approach 1:

The patent divides the influenza virus genome into separate segments, with each segment expressing a specific antigen. This segmentation allows the virus to be attenuated (reduced pathogenicity) while maintaining immunogenicity, as the virus cannot revert to wild-type form without acquiring all necessary genetic changes across multiple segments simultaneously.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent extracts and removes the M2 gene from the influenza virus genome to create the attenuated vaccine strain. By taking out this essential gene, the virus loses its ability to cause disease while retaining the capacity to present other viral antigens to the immune system, thereby preventing reversion to pathogenic forms.

Inventive Principle:
Principle #2Taking out (Extraction)

2Ease of operation

If conventional vaccine administration methods are used, then vaccine delivery is simple, but immunogenicity and effectiveness deteriorate

Engineering Contradiction:
Improvevaccine administration simplicityVSAvoidvaccine immunogenicity
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The patent employs microneedles with specific local properties (micro-scale dimensions, controlled geometry) to deliver vaccine directly to the immunologically active dermal layer. This local quality enhancement ensures high immunogenicity by targeting antigen-presenting cells in the skin, while the overall administration process remains simple and painless.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent changes the physical parameters of vaccine delivery by using microneedles instead of traditional hypodermic needles. This parameter change (from macro-scale needle insertion to micro-scale puncture) enhances immunogenicity through improved antigen delivery to immune cells, while maintaining ease of operation as the device requires minimal training to use.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS20250090649A1Influenza virus mutants and uses therefor
Publication Date: 2025.03.20 FLUGEN INC
  • US20250090649A1 patent drawing
  • US20250090649A1 patent drawing
  • US20250090649A1 patent drawing

AI summary

Disclosed herein are compositions and methods related to mutant viruses, and in particular, mutant influenza viruses. The mutant viruses disclosed herein include a mutant M2 sequence, and are useful in immunogenic compositions, e.g., as vaccines. Also disclosed herein are methods, compositions and cells for propagating the viral mutants, and methods, devices and compositions related to vaccination.