RNA Polypeptide Vaccine Kit for Immune Response

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Solution Overview

Problem

Current DNA-based vaccines face safety concerns regarding integration into the host genome and potential uncontrolled propagation, while RNA vaccines are susceptible to degradation and lack efficient cellular uptake.

Innovation Solution

The development of immunogenic compositions comprising a self-replicating RNA molecule encoding a polypeptide antigen and a separate polypeptide antigen, delivered in a kit format for sequential administration, enhances immune response by providing antigenic epitopes in both RNA and polypeptide forms, potentially using alphavirus-derived RNA replicons and adjuvants like MF59.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If DNA-based vaccines are used, then cellular immune response is generated, but safety concerns arise regarding integration into host genome and uncontrolled propagation

Engineering Contradiction:
ImprovesafetyVSAvoidintegration into host genome
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent extracts the antigen-encoding sequence from the DNA vaccine context and transfers it to an RNA-based delivery system. By using RNA instead of DNA, the invention eliminates the risk of genomic integration while maintaining the ability to induce cellular immune responses through expression of the antigen in antigen-presenting cells.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The invention changes the fundamental parameter of the genetic material from DNA to RNA. This parameter change resolves the safety concern about genomic integration, as RNA does not integrate into the host genome like DNA can. The RNA is transient and degrades naturally, providing a safer alternative while maintaining immunogenicity.

Inventive Principle:
Principle #35Parameter changes

2Ease of operation

If RNA vaccines are used, then degradation susceptibility increases, but cellular uptake efficiency improves

Engineering Contradiction:
Improvecellular uptakeVSAvoidstability
Core Design Contradiction:
Ease of operationVSDuration of action of stationary object

Solution Approach 1:

The patent employs an adjuvant as an intermediary substance that facilitates the delivery and stabilization of RNA in the vaccine composition. The adjuvant protects the RNA from degradation while enhancing its cellular uptake and immunogenicity, effectively resolving the contradiction between RNA stability and cellular uptake efficiency.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The invention creates a composite vaccine composition combining RNA with adjuvants. This composite formulation provides both the benefits of RNA (transient expression, safety) and the stabilizing effects of adjuvants, while also enhancing cellular uptake and immune response.

Inventive Principle:
Principle #40Composite materials

3Quantity of substance

If only RNA component is administered, then antigen expression is achieved, but antibody titers are insufficient

Engineering Contradiction:
Improveantibody titerVSAvoidimmune response strength
Core Design Contradiction:
Quantity of substanceVSProductivity

Solution Approach 1:

The patent merges two immunogenic components into a single vaccine composition: RNA encoding an antigen and a separate antigen or adjuvant. This combination synergistically enhances the immune response, producing higher antibody titers and more robust cellular immunity than RNA alone, while maintaining the safety advantages of RNA-based delivery.

Inventive Principle:
Principle #5Merging (Combining)

4Ease of manufacture

If DNA vaccine is used, then manufacturing simplicity is maintained, but safety concerns regarding uncontrolled propagation arise

Engineering Contradiction:
Improvemanufacturing simplicityVSAvoiduncontrolled propagation
Core Design Contradiction:
Ease of manufactureVSObject-generated harmful factors

Solution Approach 1:

The invention extracts the antigen-encoding sequence from the DNA context and implements it in an RNA-based system. This extraction eliminates the propagation risks associated with DNA while preserving the manufacturing advantages of using a nucleic acid-based platform that can be produced through established in vitro transcription methods.

Inventive Principle:
Principle #2Taking out (Extraction)

Data Source

PatentUS11058762B2Immunogenic compositions and uses thereof
Publication Date: 2021.07.13 GLAXOSMITHKLINE BIOLOGICALS SA
  • US11058762B2 patent drawing
  • US11058762B2 patent drawing
  • US11058762B2 patent drawing

AI summary

This invention generally relates to immunogenic compositions that comprise an RNA component and a polypeptide component. Immunogenic compositions that deliver antigenic epitopes in two different forms—a first epitope from a pathogen, in RNA-coded form; and a second epitope from the same pathogen, in polypeptide form—are effective in inducing immune response to the pathogen. The invention also relates to a kit comprising an RNA-based priming composition and a polypeptide-based boosting composition. The kit may be used for sequential administration of the priming and the boosting compositions.