T cell receptor therapeutics: immunological targeting of the intracellular cancer proteome

被引:0
作者
Christopher A. Klebanoff
Smita S. Chandran
Brian M. Baker
Sergio A. Quezada
Antoni Ribas
机构
[1] Human Oncology and Pathogenesis Program,Memorial Sloan Kettering Cancer Center (MSKCC)
[2] Parker Institute for Cancer Immunotherapy,Weill Cornell Medical College
[3] Cornell University,Department of Chemistry and Biochemistry
[4] University of Notre Dame,The Harper Cancer Research Institute
[5] University of Notre Dame,Cancer Immunology Unit, Research Department of Haematology
[6] University College London Cancer Institute,Cancer Research UK Lung Cancer Centre of Excellence
[7] University College London Cancer Institute,undefined
[8] Achilles Therapeutics,undefined
[9] Jonsson Comprehensive Cancer Center at the University of California,undefined
[10] Los Angeles (UCLA),undefined
来源
Nature Reviews Drug Discovery | 2023年 / 22卷
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摘要
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.
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页码:996 / 1017
页数:21
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