Abstract

T cell engineering with antigen-specific T cell receptors (TCRs) has allowed the generation of increasingly specific, reliable, and versatile T cell products with near-physiological features. However, a broad applicability of TCR-based therapies in cancer is still limited by the restricted number of TCRs, often also of suboptimal potency, available for clinical use. In addition, targeting of tumor neoantigens with TCR-engineered T cell therapy moves the field towards a highly personalized treatment, as tumor neoantigens derive from somatic mutations and are extremely patient-specific. Therefore, relevant TCRs have to be de novo identified for each patient and within a narrow time window. The naïve repertoire of healthy donors would represent a reliable source due to its huge diverse TCR repertoire, which theoretically entails T cells for any antigen specificity, including tumor neoantigens. As a challenge, antigen-specific naïve T cells are of extremely low frequency and mostly of low functionality, making the identification of highly functional TCRs finding a “needle in a haystack.” In this review, we present the technological advancements achieved in high-throughput mapping of patient-specific neoantigens and corresponding cognate TCRs and how these platforms can be used to interrogate the naïve repertoire for a fast and efficient identification of rare but therapeutically valuable TCRs for personalized adoptive T cell therapy.

Highlights

  • T cells evolved over millions of years to protect the host from infections, through the recognition of target proteins of the pathogen via the T cell receptor (TCR) and subsequent T cell activation

  • Many efforts are required to identify new and more functional TCRs. In this big challenge for identifying tumor-specific TCRs many questions are still on debate: (i) which is the best tumor-associated antigen to target?, (ii) how could functional TCRs be identified and characterized with high-throughput?, (iii) which is the best source for TCR extraction?, and (iv) how could it be possible to predict cross-reactivity and, off-target toxicities? In this review, we discuss the great potential of the antigen-unexperienced repertoire of healthy donors as source for functional TCRs for adoptive T cell transfer (ACT), and how this can be integrated with methodologies for high-throughput tumor neoantigen identification and TCR characterization, to make possible a patient-specific ACT

  • Targeting of tumor neoantigens has emerged as the new frontier for a more efficient and safer ACT, including TCR-based therapies

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Summary

Introduction

T cells evolved over millions of years to protect the host from infections, through the recognition of target proteins of the pathogen (antigens) via the T cell receptor (TCR) and subsequent T cell activation. Thereby, TCR-activated T cells can clear target cells efficiently with high sensitivity and specificity This concept has been widely used therapeutically over the last decades to treat infections and tumors by the adoptive transfer of antigen-specific T cells [1]. T cells isolated from cancer resections showed tumor specificity and elicited potent antitumor activity when reinfused in tumor-bearing hosts [5,6] These observations paved the way for the use of ACT in cancer therapy, especially in the form of transfer of autologous, ex vivo expanded TILs [7,8,9]. The overall limited therapeutic efficacy and occurrence of related toxicities point in the direction that much broader repertoire of more functional TCR-engineered T cell products is needed. In this big challenge for identifying tumor-specific TCRs many questions are still on debate: (i) which is the best tumor-associated antigen to target?, (ii) how could functional TCRs be identified and characterized with high-throughput?, (iii) which is the best source for TCR extraction?, and (iv) how could it be possible to predict cross-reactivity and, off-target toxicities? In this review, we discuss the great potential of the antigen-unexperienced repertoire of healthy donors as source for functional TCRs for ACT, and how this can be integrated with methodologies for high-throughput tumor neoantigen identification and TCR characterization, to make possible a patient-specific ACT

Identification of Functional Tumor-Specific TCRs for Highly Personalized ACT
Generation of the Naïve TCR Repertoire
Clone-Size Distribution
Avidity of the Naïve TCR Repertoire in the Context of Tumor Antigens
Detection of Low-Frequency Antigen-Specific Naïve T Cells
High Abundance of Low Avidity TCRs
Preclinical Validation of TCR Functionality
Prediction of TCR Cross-Reactivity
Findings
Conclusions
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