CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Novel ADC and γδ T cell engager targeting CDH17 for the therapy of gastrointestinal cancers.
Novel ADC and γδ T cell engager targeting CDH17 for the therapy of gastrointestinal cancers.
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CDH17 靶向 ADC 和γδ TCE 均显示出控制 GI 癌症的良好效力和疗效。它们可以提供互补的治疗选择,可用于联合治疗。
Cadherin-17 (CDH17) 是一种细胞黏附分子,在生理条件下沿肠上皮紧密连接表达。CDH17 在胃肠道 (GI) 癌症中的异常过表达促进肿瘤生长和转移,并与患者不良预后相关。由于其在正常组织中表达受限且与恶性肿瘤密切相关,CDH17 成为胃肠道癌症的一个新兴治疗靶点。
生成了一种高亲和力抗CDH17单克隆抗体(TAVO307),并将其与auristatin衍生的细胞毒性载荷偶联,以获得靶向CDH17的抗体-药物偶联物(ADC)。同时,鉴定出一种能够激活Vδ1和Vδ2亚群γδ T细胞受体的VHH抗体,并将其与抗CDH17抗体结合,生成靶向CDH17的T细胞衔接器(TCE),以招募在肠道黏膜中丰富存在并在肿瘤免疫监视中发挥关键作用的γδ T细胞。进一步在TCE上整合了一种与IL-15受体α sushi结构域融合的减毒白细胞介素-15(IL-15),以增强γδ T细胞的扩增和激活。
基于CDH17的ADC在多种GI癌细胞系中表现出强效且选择性的细胞毒性,并在异种移植模型中实现了显著的肿瘤消退。CDH17 γδ TCE诱导了肿瘤抗原依赖性的γδ T细胞脱颗粒,并重定向Vδ1和Vδ2 T细胞以有效杀伤表达CDH17的癌细胞。IL-15融合进一步增强了γδ T细胞的扩增和活化。
Cadherin-17 (CDH17) is a cell-adhesion molecule physiologically expressed along the intestinal epithelial tight junctions. Aberrant overexpression of CDH17 in gastrointestinal (GI) cancers promotes tumor growth and metastasis and is associated with poor patient prognosis. Due to its restricted expression in normal tissues and strong association with malignancy, CDH17 represents an emerging therapeutic target for GI tract cancers.
A high-affinity anti-CDH17 monoclonal antibody (TAVO307) was generated and conjugated with auristatin-derived cytotoxic payloads to obtain CDH17-directed antibody-drug conjugates (ADCs). In parallel, a VHH antibody capable of activating γδ T cell receptors from both Vδ1 and Vδ2 subsets was identified and combined with the anti-CDH17 antibody to generate CDH17-targeted T cell engager (TCE) to recruit γδ T cells, which are abundant in the intestinal mucosa and play a critical role in tumor immunosurveillance. An attenuated interleukin-15 (IL-15) fused with the IL-15 receptor α sushi domain was further incorporated on TCE to enhance γδ T cell expansion and activation.
CDH17-based ADCs exhibited potent and selective cytotoxicity in multiple GI cancer cell lines and significant tumor regression in xenograft models. The CDH17 γδ TCE induced tumor antigen-dependent γδ T cell degranulation and redirected both Vδ1 and Vδ2 T cells to effectively kill CDH17-expressing cancer cells. IL-15 fusion further augmented γδ T cell expansion and activation.
Both CDH17-targeted ADCs and γδ TCEs demonstrated promising potency and efficacy to control GI cancers. They could offer complementary therapeutic options that could be used in combination therapy.
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