Boehringer Ingelheim Regional Center Vienna (RCV), GmbH & Co KG., Cancer Immunology & Immune Modulation, Vienna, Austria.
Boehringer Ingelheim Pharmaceuticals, Inc., Translational Medicine and Clinical Pharmacology, Ridgefield, CT, United States.
Front Immunol. 2022 Sep 8;13:1008764. doi: 10.3389/fimmu.2022.1008764. eCollection 2022.
Colorectal cancer (CRC) is one of the most common cancers worldwide and demands more effective treatments. We sought to identify tumor selective CRC antigens and their therapeutic potential for cytotoxic T-cell targeting by transcriptomic and immunohistochemical analysis. LY6G6D was identified as a tumor selectively expressed CRC antigen, mainly in the microsatellite stable (MSS) subtype. A specific anti LY6G6D/CD3 T cell engager (TcE) was generated and demonstrated potent tumor cell killing and T cell activation . Ex vivo treatment of primary patient-derived CRC tumor slice cultures with the LY6G6D/CD3 TcE led to IFNγ secretion in LY6G6D positive tumor samples. , LY6G6D/CD3 TcE monotherapy demonstrated tumor regressions in pre-clinical mouse models of engrafted human CRC tumor cells and PBMCs. Lastly, 2D and 3D cocultures of LY6G6D positive and negative cells were used to explore the bystander killing of LY6G6D negative cells after specific activation of T cells by LY6G6D positive cells. LY6G6D/CD3 TcE treatment was shown to lyse target negative cells in the vicinity of target positive cells through a combined effect of IFNγ, TNFα and Fas/FasL. In summary, LY6G6D was identified as a selectively expressed CRC antigen that can be utilized to potently re-direct and activate cytotoxic T-cells to lyse LY6G6D expressing CRC using a TcE. This effect can be spread to target negative neighboring tumor cells, potentially leading to improved therapeutic efficacy.
结直肠癌(CRC)是全球最常见的癌症之一,需要更有效的治疗方法。我们通过转录组学和免疫组织化学分析,旨在鉴定肿瘤选择性 CRC 抗原及其用于细胞毒性 T 细胞靶向的治疗潜力。LY6G6D 被鉴定为一种肿瘤选择性表达的 CRC 抗原,主要在微卫星稳定(MSS)亚型中表达。生成了一种特异性抗 LY6G6D/CD3 T 细胞衔接器(TcE),并证明其具有强大的肿瘤细胞杀伤和 T 细胞激活作用。用 LY6G6D/CD3 TcE 对原发性患者来源的 CRC 肿瘤切片培养物进行体外处理,导致 LY6G6D 阳性肿瘤样本中 IFNγ 的分泌。在植入人 CRC 肿瘤细胞和 PBMC 的临床前小鼠模型中,LY6G6D/CD3 TcE 单药治疗显示出肿瘤消退。最后,使用 2D 和 3D 共培养物研究了 LY6G6D 阳性和阴性细胞在 LY6G6D 阳性细胞特异性激活 T 细胞后对 LY6G6D 阴性细胞的旁观者杀伤作用。LY6G6D/CD3 TcE 治疗通过 IFNγ、TNFα 和 Fas/FasL 的联合作用,显示出在靶阳性细胞附近裂解靶阴性细胞的作用。总之,LY6G6D 被鉴定为一种选择性表达的 CRC 抗原,可用于通过 TcE 有效地重新定向和激活细胞毒性 T 细胞,以裂解表达 LY6G6D 的 CRC。这种效应可以传播到靶阴性相邻肿瘤细胞,从而潜在地提高治疗效果。