Antigen Binding Domains for CD70 and GPC3 Targeting
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Solution Overview
Problem
Current cancer therapies face challenges in effectively targeting and eliminating cancer cells, particularly those expressing CD70, GPC3, and IL13Rα2 proteins, which are often involved in tumor progression and resistance to treatment.
Innovation Solution
Development of antigen binding domains, specifically heavy chain variable domains (VH) with defined complementarity determining regions (CDR) for antibodies targeting CD70, GPC3, and IL13Rα2, integrated into chimeric antigen receptors (CARs) or chimeric fusion proteins, enabling specific binding and intracellular signaling for enhanced cancer cell targeting and elimination.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If current cancer therapies are used to target cancer cells expressing CD70, GPC3, and IL13Rα2 proteins, then treatment coverage is provided, but effectiveness is reduced due to tumor progression and treatment resistance
Solution Approach 1:
The patent modifies the structure of chimeric antigen receptors by changing parameters such as the antigen-binding domain configuration, CDR sequences, and domain architecture to create novel CAR variants with improved ability to recognize and bind to cancer cells expressing CD70, GPC3, and IL13Rα2, thereby overcoming treatment resistance
Solution Approach 2:
The invention creates composite chimeric antigen receptors that integrate multiple functional domains including antigen-binding domains, transmembrane domains, and intracellular signaling domains in a unified structure, enabling simultaneous targeting of multiple cancer-associated proteins and enhanced therapeutic effectiveness
2Measurement precision
If antigen binding domains with defined CDR regions are developed for targeting specific proteins, then binding specificity is improved, but development complexity increases
Solution Approach 1:
The patent segments the antibody structure into distinct functional domains with defined complementarity determining regions (CDR1, CDR2, CDR3) in the variable heavy chain, allowing independent optimization of each domain's binding characteristics while maintaining overall structural organization
Solution Approach 2:
The invention develops antigen-binding domains with universal structural frameworks that can be adapted to target multiple different antigens (CD70, GPC3, IL13Rα2) by modifying only the CDR regions, thereby achieving high binding specificity without requiring complete redesign of the entire antibody structure
Data Source
AI summary
Compositions and methods for binding to target antigens. Compositions comprising variable heavy chain domains with binding specificity to CD70, GPC3, IL13Ralpha2 and Cadherin CDH17 antigens.


