Abstract 4768: Development of fully human TCR-mimic antibodies targeting intracellular tumor antigens using humanized RenTCR-mimic transgenic mice

Abstract T cell receptors (TCRs), a promising therapeutic strategy for targeting intracellular antigens, can specifically recognize antigen peptide presented by human lymphocyte antigen (HLA) and mediate T cell responses to eliminate tumor cells. However, the low affinity of TCRs presents a great challenge to their broader clinical application. TCR-mimic (TCRm) antibodies, with similar antigen recognition capabilities as TCRs but higher affinity, offer a solution to these limitations, enabling the targeting of previously undruggable cancer antigens. Neverthelss, specificity remains a major challenge to ensure therapeutic accuracy and patient safety, as TCRm antibodies need to precisely target a single tumor-specific peptide antigen presented by HLA rather than other similar peptides. Using RenTCR-mimic transgenic mice, we describe the generation and preclinical evaluation of fully human TCRm antibodies by fusing them with a humanized anti-CD3 scFv to form T cell engager or assembled on T cell surface to build TCRm-T cells, further to specifically redirect T cells to lysis tumors by our proprietary RenTCR-mimic platform. We determine cross-reactive peptide sequences predicted by in silico or known off-target sequences. We further confirm the specificity and safety of TCRm antibodies. Despite low density antigen copies, TCRm antibodies elicited antibody-mediated T-cell recognition and cytotoxicity against antigen peptide-HLA complexes-restricted cell lines. Based on these methods, we perform screens to validate TCRm antibodies specificity. These experiments led us to discriminate between the target peptide and the potential off-target peptides presented by HLA and highlight the therapeutics potential of TCRm antibodies in tumor immunotherapy, offering a novel approach to expanding the repertoire of druggable cancer targets. Citation Format: Han Zhang, Wanbo Tang, Jun Du, Yue Zhang, Limin Zhao, Xin Jiao, Baihong Liu, Yi Yang. Development of fully human TCR-mimic antibodies targeting intracellular tumor antigens using humanized RenTCR-mimic transgenic mice [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 4768.

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Publication Details

Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-4768
Primary Topic
Monoclonal and Polyclonal Antibodies Research
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article
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article

Abstract 4768: Development of fully human TCR-mimic antibodies targeting intracellular tumor antigens using humanized RenTCR-mimic transgenic mice

Wanbo Tang, Limin Zhao, Baihong Liu, Han Zhang et al.
Cancer Research
Monoclonal and Polyclonal Antibodies Research
article

Abstract 4768: Development of fully human TCR-mimic antibodies targeting intracellular tumor antigens using humanized RenTCR-mimic transgenic mice

Wanbo Tang, Limin Zhao, Baihong Liu, Han Zhang, Jun Du, Xin Jiao, Yue Zhang, Yi Yang
article en

Abstract

Abstract T cell receptors (TCRs), a promising therapeutic strategy for targeting intracellular antigens, can specifically recognize antigen peptide presented by human lymphocyte antigen (HLA) and mediate T cell responses to eliminate tumor cells. However, the low affinity of TCRs presents a great challenge to their broader clinical application. TCR-mimic (TCRm) antibodies, with similar antigen recognition capabilities as TCRs but higher affinity, offer a solution to these limitations, enabling the targeting of previously undruggable cancer antigens. Neverthelss, specificity remains a major challenge to ensure therapeutic accuracy and patient safety, as TCRm antibodies need to precisely target a single tumor-specific peptide antigen presented by HLA rather than other similar peptides. Using RenTCR-mimic transgenic mice, we describe the generation and preclinical evaluation of fully human TCRm antibodies by fusing them with a humanized anti-CD3 scFv to form T cell engager or assembled on T cell surface to build TCRm-T cells, further to specifically redirect T cells to lysis tumors by our proprietary RenTCR-mimic platform. We determine cross-reactive peptide sequences predicted by in silico or known off-target sequences. We further confirm the specificity and safety of TCRm antibodies. Despite low density antigen copies, TCRm antibodies elicited antibody-mediated T-cell recognition and cytotoxicity against antigen peptide-HLA complexes-restricted cell lines. Based on these methods, we perform screens to validate TCRm antibodies specificity. These experiments led us to discriminate between the target peptide and the potential off-target peptides presented by HLA and highlight the therapeutics potential of TCRm antibodies in tumor immunotherapy, offering a novel approach to expanding the repertoire of druggable cancer targets. Citation Format: Han Zhang, Wanbo Tang, Jun Du, Yue Zhang, Limin Zhao, Xin Jiao, Baihong Liu, Yi Yang. Development of fully human TCR-mimic antibodies targeting intracellular tumor antigens using humanized RenTCR-mimic transgenic mice [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 4768.

Cancer ResearchVol. 85(8_Supplement_1)
Beijing Biocytogen (China) (CN)
Openalex Percentile: Top 87%
Monoclonal and Polyclonal Antibodies Research
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