moDC-Targeted Mucosal Vaccine Adjuvant for Durable Lung Immunity

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Solution Overview

Problem

There are few effective mucosal vaccines due to challenges in developing safe and potent mucosal adjuvants.

Innovation Solution

A vaccine composition comprising an antigen, a cyclic dinucleotide (CDN), soluble tumor necrosis factor (TNF), and a CD64 antibody or antibody fragment, targeting monocyte-derived dendritic cells (moDCs) to induce lung mucosal antibody responses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If mucosal vaccines are developed to induce protective immunity against mucosal pathogens, then vaccine efficacy is improved, but development of safe and effective mucosal adjuvants becomes more difficult

Engineering Contradiction:
Improvevaccine efficacyVSAvoidadjuvant development complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent uses monocyte-derived dendritic cells (moDCs) as intermediary cells to bridge the gap between the vaccine antigen and the immune system. moDCs are targeted specifically to process and present antigen in the mucosal tissue, facilitating effective immune response without requiring complex adjuvant formulations. This intermediary approach simplifies vaccine development while maintaining high efficacy.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent applies local quality by targeting moDCs specifically in the mucosal tissue environment rather than using system-wide adjuvants. The vaccine composition is designed to act locally at the mucosal surface, inducing protective immunity precisely where needed against mucosal pathogens, thereby improving efficacy without the complexity of systemic adjuvant development.

Inventive Principle:
Principle #3Local quality

2Productivity

If moDCs are targeted to present antigen, then antibody response is enhanced, but specificity of immune response may be reduced

Engineering Contradiction:
Improveantibody responseVSAvoidimmune response specificity
Core Design Contradiction:
ProductivityVSMeasurement precision

Solution Approach 1:

The patent employs parameter changes by modulating the functional state of moDCs through targeted cytokine signaling (e.g., CD40L, CD70, CD27 interactions). These parameter modifications enhance the antibody response capability of moDCs while maintaining their specificity for pathogen antigens. The controlled adjustment of moDC activation parameters ensures both high antibody production and specific immune response.

Inventive Principle:
Principle #35Parameter changes

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

Generates efficacious vaccine responses and long-term memory responses on mucosal surfaces, enhancing protection against pathogens.

Implementation Method 1

a CD64 antibody or antibody fragment, targeting monocyte-derived dendritic cells (moDCs)

Methodology Applied
Scientific EffectAntibody binding:

Implementation Method 2

a cyclic dinucleotide (CDN), soluble tumor necrosis factor (TNF), and a CD64 antibody or antibody fragment, targeting monocyte-derived dendritic cells (moDCs)

Methodology Applied
Scientific EffectCyclic dinucleotide activation:

Implementation Method 3

Generates efficacious vaccine responses and long-term memory responses on mucosal surfaces, enhancing protection against pathogens

Methodology Applied
Scientific EffectImmune response generation:

Data Source

PatentUS12569557B2Targeting moDC to enhance vaccine efficacy on mucosal surface
Publication Date: 2026.03.10 UNIV OF FLORIDA RESEARCH FOUNDATION INC
  • US12569557B2 patent drawing
  • US12569557B2 patent drawing
  • US12569557B2 patent drawing

AI summary

Described herein are novel vaccine compositions and methods for use thereof in inducing an immune response in a subject especially aged subjects. Specifically exemplified are vaccine compositions that include an antigen; a cyclic dinucleotide; soluble tumor necrosis factor (TNF); or a CD64 antibody or antibody fragment. Optionally, the vaccine composition comprises a TNF conjugated with a moDC targeting moiety in addition to or in place of TNF or CD64 antibody or antibody fragment, or both TNF and CD64 antibody or antibody fragment.