Recombinant Protein Inducing Immune Tolerance for Multiple Sclerosis

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Solution Overview

Problem

Current treatments for multiple sclerosis, such as disease-modifying therapy drugs, only reduce recurrence and delay progression but are ineffective for severe cases and have significant side effects, necessitating a safer and more effective approach.

Innovation Solution

A recombinant protein comprising HSP65 and 6-segment tandem repeat antigen epitope polypeptide MOG35-55, connected through a flexible joint, is developed to induce immune tolerance and used in vaccines or drugs administered intranasally to prevent multiple sclerosis.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If disease modifying therapy drugs are used to treat multiple sclerosis, then the recurrence rate is reduced and disease progression is delayed, but the drugs are ineffective in severe cases and cause strong side effects

Engineering Contradiction:
Improveeffectiveness of treatmentVSAvoidside effects
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent uses the autoantigen MOG35-55, which normally triggers harmful autoimmune responses, and converts this harm into benefit by immunizing with the autoantigen to induce immune tolerance. This approach transforms the harmful autoimmune reaction into a protective tolerance mechanism, eliminating the need for external DMT drugs and their associated side effects.

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Solution Approach 2:

Instead of suppressing the immune response to MOG35-55 (the conventional approach), the patent inverts the strategy by actively inducing immune tolerance to the autoantigen. This inversion of the immune response strategy leads to protective effects without the harmful side effects of conventional DMT drugs.

Inventive Principle:
Principle #13The other way round (Inversion)

2Reliability

If conventional DMT drugs are used, then recurrence rate is reduced, but the treatment does not cure the disease and severe cases remain ineffective

Engineering Contradiction:
Improvetreatment effectivenessVSAvoidcure capability
Core Design Contradiction:
ReliabilityVSManufacturing precision

Solution Approach 1:

The patent applies preliminary action by immunizing with the autoantigen MOG35-55 before the disease progresses severely. This preventive immunization induces immune tolerance that can stop disease progression and achieve cure, rather than merely treating symptoms or reducing recurrence after disease establishment.

Inventive Principle:
Principle #10Preliminary action

3Object-affected harmful factors

If autoantigen immunization is used to induce immune tolerance, then safe and effective treatment is achieved, but the immune response must be precisely controlled

Engineering Contradiction:
Improvesafety of treatmentVSAvoidimmune response control complexity
Core Design Contradiction:
Object-affected harmful factorsVSDevice complexity

Solution Approach 1:

The patent applies local quality by using a specific peptide sequence (MOG35-55) from the autoantigen rather than the entire protein. This localized peptide approach allows precise control of the immune response to specific epitopes, simplifying the complexity of inducing targeted immune tolerance without affecting other autoantigen regions.

Inventive Principle:
Principle #3Local quality

Data Source

PatentUS20240197847A1Recombinant protein capable of resisting multiple sclerosis and preparation method and application thereof
Publication Date: 2024.06.20 INST OF ZOOLOGY GUANGDONG ACAD OF SCI
  • US20240197847A1 patent drawing
  • US20240197847A1 patent drawing
  • US20240197847A1 patent drawing

AI summary

The present invention discloses a recombinant protein capable of resisting multiple sclerosis and a preparation method and application thereof, and belongs to the technical field of biopharmacy. The recombinant protein of the present invention comprises Mycobacterium tuberculosis heat shock protein 65 and 6-segment tandem repeat myelin oligodendroglia glycoprotein antigen epitope polypeptides with multiple sclerosis autoimmune antigen characteristics at the 33rd-55th sites. The recombinant protein capable of resisting multiple sclerosis is used for preparing multiple sclerosis vaccines and/or preparing multiple sclerosis drugs. The present invention can play a role in preventing multiple sclerosis and can avoid side effects caused by most of disease modifying therapy (DMT) drugs.