PNA-CPP Adjuvants for Mucosal Vaccine Immunity

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Solution Overview

Problem

Current vaccines, especially inactivated and subunit vaccines, face challenges in generating sufficient immunity due to lack of infectivity and mucosal affinity, requiring adjuvants with immunostimulatory capabilities, while existing adjuvants like aluminum salts have limitations, particularly in combination with mucosal vaccines.

Innovation Solution

Modification of peptide nucleic acids (PNAs) with cell penetrating peptides (CPPs), such as TAT from HIV, to create adjuvants that enhance vaccine efficacy and safety by promoting immune responses through both injection and mucosal administration.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If inactivated vaccines or subunit vaccines are used, then safety is improved, but immune response capability deteriorates

Engineering Contradiction:
ImprovesafetyVSAvoidimmune response capability
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent combines inactivated/subunit vaccines (safe but weak immunogenicity) with PNA-CPP adjuvants (potent immunostimulatory agents) to create a composite vaccine system that maintains safety while significantly enhancing immune response capability through synergistic interaction between antigen and adjuvant

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The invention creates a composite vaccine formulation consisting of inactivated or subunit antigen components combined with PNA-CPP adjuvant molecules, where the composite system produces immune responses superior to either component alone while maintaining the safety profile of the inactivated/subunit approach

Inventive Principle:
Principle #40Composite materials

2Productivity

If live attenuated vaccines are used, then immune response capability is improved, but safety deteriorates

Engineering Contradiction:
Improveimmune response capabilityVSAvoidsafety
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent extracts the immunostimulatory function from live attenuated vaccines and transfers it to the PNA-CPP adjuvant system, allowing inactivated/subunit vaccines to achieve similar immune response capability without the safety risks associated with live viral components

Inventive Principle:
Principle #2Taking out (Extraction)

3Productivity

If aluminum salts adjuvant is used, then immune response is improved, but mucosal affinity deteriorates

Engineering Contradiction:
Improveimmune responseVSAvoidmucosal affinity
Core Design Contradiction:
ProductivityVSAdaptability or versatility

Solution Approach 1:

The patent fundamentally changes the chemical and physical parameters of the adjuvant system by using PNA-CPP molecules with specific properties (cell-penetrating capability, mucosal affinity, immunostimulatory activity) that enable effective immune response enhancement through mucosal routes, unlike traditional aluminum salt adjuvants

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS12016920B2Adjuvant based on peptide nucleic acid
Publication Date: 2024.06.25 DENKA CO LTD
  • US12016920B2 patent drawing
  • US12016920B2 patent drawing
  • US12016920B2 patent drawing

AI summary

Provided are an adjuvant useful for preparing a vaccine having high efficacy and high safety, and a vaccine composition comprising the adjuvant.The adjuvant comprises a peptide nucleic acid to which a cell penetrating peptide is bound.