T cell receptor therapeutics: immunological targeting of the intracellular cancer proteome
Christopher A Klebanoff1, Smita S Chandran2,3,4, Brian M Baker5,6
1Memorial Sloan Kettering Cancer Center (MSKCC), Human Oncology and Pathogenesis Program, New York, NY, USA. klebanoc@mskcc.org.
Abstract:
The T cell receptor (TCR) complex is a naturally occurring antigen sensor that detects, amplifies and coordinates cellular immune responses to epitopes derived from cell surface and intracellular proteins. Thus, TCRs enable the targeting of proteins selectively expressed by cancer cells, including neoantigens, cancer germline antigens and viral oncoproteins. As such, TCRs have provided the basis for an emerging class of oncology therapeutics. Herein, we review the current cancer treatment landscape using TCRs and TCR-like molecules. This includes adoptive cell transfer of T cells expressing endogenous or engineered TCRs, TCR bispecific engagers and antibodies specific for human leukocyte antigen (HLA)-bound peptides (TCR mimics). We discuss the unique complexities associated with the clinical development of these therapeutics, such as HLA restriction, TCR retrieval, potency assessment and the potential for cross-reactivity. In addition, we highlight emerging clinical data that establish the antitumour potential of TCR-based therapies, including tumour-infiltrating lymphocytes, for the treatment of diverse human malignancies. Finally, we explore the future of TCR therapeutics, including emerging genome editing methods to safely enhance potency and strategies to streamline patient identification.
Insights
T cell receptor (TCR) therapies offer a promising approach to cancer treatment by targeting cancer-specific antigens. This review covers current TCR-based treatments, challenges, and future directions in oncology.
Area of Science:
- Immunology
- Oncology
- Biotechnology
Background:
- The T cell receptor (TCR) complex acts as a natural sensor for cellular immune responses.
- TCRs can target cancer-specific antigens like neoantigens, making them valuable for cancer therapy.
Purpose of the Study:
- To review the current landscape of TCR-based cancer therapeutics.
- To discuss the complexities and challenges in the clinical development of TCR therapies.
- To highlight emerging data and future directions for TCR therapeutics.
Main Methods:
- Review of current literature on TCR-based oncology treatments.
- Discussion of adoptive cell transfer, TCR bispecific engagers, and TCR mimics.
- Analysis of clinical development challenges including HLA restriction and cross-reactivity.
Main Results:
- TCR-based therapies show antitumour potential in diverse human malignancies.
- Emerging clinical data support the efficacy of TCR-based treatments.
- Genome editing and patient identification strategies are advancing TCR therapy.
Conclusions:
- TCR therapeutics represent an emerging and promising class of oncology treatments.
- Overcoming clinical development complexities is key to advancing TCR therapies.
- Future strategies aim to enhance potency and patient selection for TCR-based treatments.
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