TCR mimic compounds for pHLA targeting with high potency modalities in oncology

Hans-Peter Gerber1, Leonard G Presta1

  • 1ADC Research and Development Codeable Therapeutics, Palo Alto, CA, United States.

Frontiers in Oncology
|November 7, 2022
PubMed

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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