CD96 Binding Proteins for Blocking CD155 Immune Inhibition
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Solution Overview
Problem
There is a need for improved antigen binding proteins that target CD96 for the treatment of diseases, as little is known about its function and existing technologies have not effectively addressed its role in immune regulation.
Innovation Solution
Development of CD96 binding proteins, nucleic acid constructs, expression vectors, and recombinant host cells to produce CD96 binding proteins, which can be used in pharmaceutical compositions for therapeutic applications.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If CD96 binding proteins are developed to block CD155-CD96 interaction, then immune inhibition is inhibited and therapeutic benefit is improved, but knowledge about CD96 function remains limited and mechanism understanding is insufficient
Solution Approach 1:
The patent segments the CD96 receptor into its ligand-binding domain (extracellular domain) and develops binding proteins that specifically target this domain. This segmentation allows blocking of the CD155-CD96 interaction without requiring complete understanding of the entire CD96 signaling mechanism, enabling therapeutic development despite limited functional knowledge of CD96
Solution Approach 2:
The patent introduces CD96 binding proteins as intermediary molecules that mediate the blocking of CD155 binding to CD96. These binding proteins serve as the active therapeutic agents that interfere with the natural ligand-receptor interaction, providing therapeutic benefit while the actual mechanism of CD96 signaling can be studied separately through research
2Adaptability or versatility
If CD96 binding proteins are used to treat diseases, then therapeutic applications are expanded, but the complexity of developing and characterizing new antigen binding proteins increases
Solution Approach 1:
The patent develops CD96 binding proteins with universal application potential across multiple disease states involving CD96-mediated immune inhibition. The binding proteins are designed to target the conserved CD96 receptor structure, enabling broad therapeutic applicability against different cancers and immune-related diseases while using a standardized development platform for antigen binding proteins
Solution Approach 2:
The patent employs parameter changes in the development process, including optimizing binding affinity, specificity, and stability parameters of the CD96 binding proteins. By systematically adjusting these parameters during development and characterization, the patent manages complexity through structured optimization rather than unguided experimentation
Data Source
AI summary
The present disclosure relates to compositions for treating CD96 mediated diseases, and related methods.


