CD40 DNA Aptamer Adjuvants for Low-Immunogenicity Vaccines

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Solution Overview

Problem

Existing CD40 agonists, such as anti-CD40 monoclonal antibodies, are costly and highly immunogenic, making them impractical for use as vaccine adjuvants in industries with tight profit margins, and there is a need for alternative biomolecules with low-immunogenicity for enhancing immune responses.

Innovation Solution

Development of immunostimulatory nucleic acids, specifically DNA aptamers with high specificity and affinity for CD40, which are produced through SELEX and used to create immunostimulatory complexes with antigens to enhance immune responses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If anti-CD40 monoclonal antibodies are used as CD40 agonists, then immune response stimulation is achieved, but production cost increases and immunogenicity worsens

Engineering Contradiction:
Improveimmune response stimulationVSAvoidhigh immunogenicity
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent uses DNA aptamers as simplified copies that mimic the function of anti-CD40 monoclonal antibodies. These aptamers bind to CD40 and stimulate immune responses without the high immunogenicity and production costs associated with full monoclonal antibodies, achieving the desired immune stimulation through a less complex molecular structure

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The patent employs DNA aptamers as cost-effective alternatives to expensive monoclonal antibodies. DNA aptamers can be synthesized more cheaply and are less immunogenic, making them suitable for applications where cost and immunogenicity are concerns while still achieving the necessary immune response stimulation

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

2Reliability

If anti-CD40 monoclonal antibodies are used as vaccine adjuvants, then immune response enhancement is achieved, but production cost increases

Engineering Contradiction:
Improveimmune response enhancementVSAvoidproduction cost
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent replaces expensive monoclonal antibody adjuvants with DNA aptamer copies that replicate the essential CD40-stimulating function. This substitution dramatically reduces production costs while maintaining the ability to enhance immune responses in vaccine applications

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The patent uses synthetically produced DNA aptamers as inexpensive substitutes for costly monoclonal antibody adjuvants. The DNA-based approach enables lower-cost manufacturing and distribution of vaccine adjuvants while preserving the desired immunoenhancement effects

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The DNA aptamers effectively stimulate immune responses, demonstrating elevated antibody titers and robust immune activation, offering a cost-effective and less immunogenic alternative to traditional CD40 agonists.

Implementation Method 1

DNA aptamers with high specificity and affinity for the CD40 protein, which are synthesized to mimic the CD40-CD40L interaction

Methodology Applied
Scientific EffectMolecular recognition and binding:

Data Source

PatentUS12618074B2CD40 specific DNA aptamers as vaccine adjuvants
Publication Date: 2026.05.05 TEXAS A&M UNIVERSITY
  • US12618074B2 patent drawing
  • US12618074B2 patent drawing
  • US12618074B2 patent drawing

AI summary

The present invention provides immunostimulatory nucleic acids that have an affinity to a specific target protein. The present invention also provides templates and methods for making and using the immunostimulatory nucleic acids. Further, methods for linking the immunostimulatory nucleic acids to antigens and using the resulting complexes to enhance an immune response are provided.