Schoenfeld Katrin, Habermann Jan, Wendel Philipp, Harwardt Julia, Ullrich Evelyn, Kolmar Harald
Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Goethe University, Department of Pediatrics, Experimental Immunology and Cell Therapy, 60590 Frankfurt am Main, Germany.
Mol Ther Oncol. 2024 Jul 19;32(3):200850. doi: 10.1016/j.omton.2024.200850. eCollection 2024 Sep 19.
T cell-derived cancers are hallmarked by heterogeneity, aggressiveness, and poor clinical outcomes. Available targeted therapies are severely limited due to a lack of target antigens that allow discrimination of malignant from healthy T cells. Here, we report a novel approach for the treatment of T cell diseases based on targeting the clonally rearranged T cell receptor displayed by the cancerous T cell population. As a proof of concept, we identified an antibody with unique specificity toward a distinct T cell receptor (TCR) and developed antibody-drug conjugates, precisely recognizing and eliminating target T cells while preserving overall T cell repertoire integrity and cellular immunity. Our anti-TCR antibody-drug conjugates demonstrated effective receptor-mediated cell internalization, associated with induction of cancer cell death with strong signs of apoptosis. Furthermore, cell proliferation-inhibiting bystander effects observed on target-negative cells may contribute to the molecules' anti-tumor properties precluding potential tumor escape mechanisms. To our knowledge, this represents the first anti-TCR antibody-drug conjugate designed as custom-tailored immunotherapy for T cell-driven pathologies.
T细胞源性癌症的特点是异质性、侵袭性和较差的临床预后。由于缺乏能够区分恶性T细胞与健康T细胞的靶抗原,现有的靶向治疗方法受到严重限制。在此,我们报告一种基于靶向癌性T细胞群体所展示的克隆重排T细胞受体来治疗T细胞疾病的新方法。作为概念验证,我们鉴定出一种对独特T细胞受体(TCR)具有独特特异性的抗体,并开发了抗体-药物偶联物,能够精确识别并清除靶T细胞,同时保持整体T细胞库完整性和细胞免疫。我们的抗TCR抗体-药物偶联物显示出有效的受体介导的细胞内化作用,与诱导癌细胞死亡及强烈的凋亡迹象相关。此外,在靶阴性细胞上观察到的抑制细胞增殖的旁观者效应可能有助于该分子的抗肿瘤特性,排除潜在的肿瘤逃逸机制。据我们所知,这是首个设计用于T细胞驱动病症的定制免疫疗法的抗TCR抗体-药物偶联物。