Nucleic Acid Molecules for Targeted Immune Response Induction

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Solution Overview

Problem

Current immunotherapy and gene therapy methods are imperfect and lack effective solutions for treating diseases, particularly in inducing immune responses against specific proteins overexpressed in cancer cells or infectious agents.

Innovation Solution

Nucleic acid molecules are designed to encode sequences for constitutive promoters, full-length proteins, linkers, ubiquitin, and protein fragments, which are operatively connected to facilitate expression and immune response induction, including the use of nuclear localization signals for efficient cellular uptake and expression of target molecules.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If current immunotherapy and gene therapy methods are used, then treatment of diseases is achieved, but the therapies are imperfect and lack effective solutions for inducing immune responses against specific proteins

Engineering Contradiction:
Improveeffectiveness of immune response inductionVSAvoidability to treat specific diseases effectively
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent segments the target protein into multiple components: full-length protein, linker, ubiquitin, and protein fragments (at least 7 amino acid residues). This segmentation allows the immune system to recognize multiple epitopes simultaneously, enhancing the immune response while maintaining versatility for treating different diseases by targeting different protein segments.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent creates a composite therapeutic construct by operatively connecting multiple nucleic acid sequences that encode different protein components (full-length protein, linker, ubiquitin, fragments). This composite approach combines the advantages of each component to achieve reliable and versatile immune response induction against specific disease targets.

Inventive Principle:
Principle #40Composite materials

2Reliability

If nucleic acid molecules encode multiple components (full-length protein, linker, ubiquitin, fragments), then immune response induction is enhanced, but the molecular complexity increases

Engineering Contradiction:
Improveimmune response induction effectivenessVSAvoidnucleic acid molecule structure
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent merges multiple nucleic acid sequences into a single operatively connected construct that encodes full-length protein, linker, ubiquitin, and protein fragments. This merging simplifies delivery and expression while maintaining the complex functional benefits of multiple protein components for reliable immune response induction.

Inventive Principle:
Principle #5Merging (Combining)

3Measurement precision

If protein fragments of at least 7 amino acid residues are included, then immune response specificity is improved, but the precision of target recognition requires higher manufacturing precision

Engineering Contradiction:
Improvetarget protein recognition specificityVSAvoidsequence encoding accuracy
Core Design Contradiction:
Measurement precisionVSManufacturing precision

Solution Approach 1:

The patent specifies a minimum parameter for fragment length (at least 7 amino acid residues) that optimizes immune recognition without requiring excessive manufacturing precision. This parameter change balances specificity with practical manufacturability, allowing reliable target recognition while accommodating standard molecular biology techniques.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS11844824B2Nucleic acid molecules and methods of using the same
Publication Date: 2023.12.19 PEPVAX INC
  • US11844824B2 patent drawing
  • US11844824B2 patent drawing

AI summary

Nucleic acid molecules are provided herein that can be used, for example, to treat cancer or infections, or to induce an immune response in a subject, or to deliver or express a target molecule in or from a cell.