CD3 Aptamer Targeting for T Cell Labeling

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Solution Overview

Problem

Current methods lack effective and specific targeting of T cells for therapeutic and diagnostic applications, as existing technologies do not provide efficient means to selectively bind and modulate CD3 proteins on T cells.

Innovation Solution

Development of DNA and RNA aptamers that specifically bind to CD3 ε/γ or CD3 ε/δ protein complexes, allowing for targeted labeling, purification, or modulation of T cells, and their use in delivery vehicles for therapeutic agents.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If existing targeting technologies are used for T cell targeting, then general cell targeting can be achieved, but specific and efficient binding to CD3 proteins is insufficient

Engineering Contradiction:
Improvebinding specificity to CD3VSAvoidtargeting efficiency
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent employs SELEX (Systematic Evolution of Ligands by EXponential enrichment) to iteratively optimize aptamer sequences, changing nucleic acid parameters through multiple selection rounds. This process transforms random nucleic acid sequences into high-affinity binders with specific CD3 targeting capability, resolving the contradiction between binding specificity and targeting efficiency

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates synthetic nucleic acid copies (aptamers) that replicate the binding function of natural ligands but with enhanced properties. These aptamer copies can be chemically synthesized with controlled sequences that specifically recognize CD3 proteins, achieving both high specificity and efficiency that natural systems alone cannot provide

Inventive Principle:
Principle #26Copying

2Measurement precision

If aptamers are used for T cell targeting, then high specificity and affinity to CD3 proteins is achieved, but complexity in aptamer design and selection increases

Engineering Contradiction:
Improvebinding affinityVSAvoidaptamer selection process
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent develops a universal SELEX platform that can select aptamers against multiple different targets using the same basic methodology. The process universally applies to various proteins and cell surfaces, reducing the perceived complexity by showing that the same systematic approach works across different applications

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The patent divides the complex aptamer selection process into discrete, manageable segments: library preparation, selection rounds, amplification, and characterization. Each segment can be independently optimized and controlled, making the overall complex process more tractable and reproducible

Inventive Principle:
Principle #1Segmentation

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 aptamers enable precise targeting and modulation of T cells, enhancing therapeutic delivery and diagnostic capabilities by providing high specificity and affinity to CD3 proteins, thereby overcoming the limitations of existing technologies.

Implementation Method 1

aptamers that bind to CD3 and can be used to target, label or sort T cells

Methodology Applied
Scientific EffectMolecular recognition and binding:

Data Source

PatentUS20220251562A1Anti-CD3 Aptamers for Use in Cell Targeting and Labeling
Publication Date: 2022.08.11 IXAKA FRANCE
  • US20220251562A1 patent drawing
  • US20220251562A1 patent drawing
  • US20220251562A1 patent drawing

AI summary

High affinity aptamer sequences recognizing CD3 protein complex on cell surfaces are provided. The aptamers can be used as targeting moieties for delivery vehicles or as molecular components for immunotherapy, immunodiagnostics, or for isolating, purifying, or characterizing CD3+ T cells in a subject.