TCR mimic compounds for pHLA targeting with high potency modalities in oncology
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Hans-Peter Gerber1, Leonard G Presta1
1ADC Research and Development Codeable Therapeutics, Palo Alto, CA, United States.
Abstract:
pHLA complexes represent the largest class of cell surface markers on cancer cells, making them attractive for targeted cancer therapies. Adoptive cell therapies expressing TCRs that recognize tumor specific pHLAs take advantage of the unique selectivity and avidity of TCR: pHLA interactions. More recently, additional protein binding domains binding to pHLAs, known as TCR mimics (TCRm), were developed for tumor targeting of high potency therapeutic modalities, including bispecifics, ADCs, CAR T and -NK cells. TCRm compounds take advantage of the exquisite tumor specificity of certain pHLA targets, including cell lineage commitment markers and cancer testis antigens (CTAs). To achieve meaningful anti-tumor responses, it is critical that TCRm compounds integrate both, high target binding affinities and a high degree of target specificity. In this review, we describe the most advanced approaches to achieve both criteria, including affinity- and specificity engineering of TCRs, antibodies and alternative protein scaffolds. We also discuss the status of current TCRm based therapeutics developed in the clinic, key challenges, and emerging trends to improve treatment options for cancer patients treated with TCRm based therapeutics in Oncology.
Insights
TCR mimics (TCRm) offer targeted cancer therapy by binding to peptide-MHC complexes (pHLAs) on cancer cells. Engineering TCRm for high affinity and specificity is crucial for effective anti-tumor responses and improved patient outcomes.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Peptide-MHC class I (pHLAs) are abundant cancer cell surface markers, making them key targets for cancer therapies.
- TCR mimics (TCRm) are engineered protein binders that recognize pHLAs, enabling targeted delivery of potent therapeutics like bispecifics and CAR T-cells.
Purpose of the Study:
- To review advanced strategies for engineering TCRm with high binding affinity and specificity for pHLA targets.
- To discuss the clinical status of TCRm-based therapeutics and identify challenges and future trends in oncology.
Main Methods:
- Affinity and specificity engineering of T-cell receptors (TCRs), antibodies, and alternative protein scaffolds.
- Analysis of current TCRm-based therapeutic development in the clinic.
Main Results:
- TCRm compounds leverage the tumor-specific nature of pHLA targets, including cancer-testis antigens (CTAs).
- Achieving high affinity and specificity in TCRm is critical for potent anti-tumor activity.
Conclusions:
- Advanced engineering approaches are vital for optimizing TCRm-based cancer therapies.
- Further development is needed to overcome challenges and improve treatment options for cancer patients.
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