Institute of Drug Metabolism and Pharmaceutical Analysis, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, Zhejiang Province, China.
Department of Innovative Drug Discovery and Development, Zhejiang Doer Biologics Co., Ltd., Hangzhou, 310058, Zhejiang Province, China.
Cancer Immunol Immunother. 2024 Mar 30;73(5):82. doi: 10.1007/s00262-024-03673-x.
Claudin 18.2 (CLDN18.2) is a highly anticipated target for solid tumor therapy, especially in advanced gastric carcinoma and pancreatic carcinoma. The T cell engager targeting CLDN18.2 represents a compelling strategy for enhancing anti-cancer efficacy.
Based on the in-house screened anti-CLDN18.2 VHH, we have developed a novel tri-specific T cell engager targeting CLDN18.2 for gastric and pancreatic cancer immunotherapy. This tri-specific antibody was designed with binding to CLDN18.2, human serum albumin (HSA) and CD3 on T cells.
The DR30318 demonstrated binding affinity to CLDN18.2, HSA and CD3, and exhibited T cell-dependent cellular cytotoxicity (TDCC) activity in vitro. Pharmacokinetic analysis revealed a half-life of 22.2-28.6 h in rodents and 41.8 h in cynomolgus monkeys, respectively. The administration of DR30318 resulted in a slight increase in the levels of IL-6 and C-reactive protein (CRP) in cynomolgus monkeys. Furthermore, after incubation with human PBMCs and CLDN18.2 expressing cells, DR30318 induced TDCC activity and the production of interleukin-6 (IL-6) and interferon-gamma (IFN-γ). Notably, DR30318 demonstrated significant tumor suppression effects on gastric cancer xenograft models NUGC4/hCLDN18.2 and pancreatic cancer xenograft model BxPC3/hCLDN18.2 without affecting the body weight of mice.
Claudin 18.2(CLDN18.2)是实体瘤治疗的一个备受期待的靶点,特别是在晚期胃癌和胰腺癌中。靶向 CLDN18.2 的 T 细胞衔接子代表了提高抗癌疗效的一种有吸引力的策略。
基于内部筛选的抗 CLDN18.2 VHH,我们开发了一种新型三特异性 T 细胞衔接子,用于治疗胃癌和胰腺癌的免疫疗法。该三特异性抗体的设计目的是与 CLDN18.2、人血清白蛋白(HSA)和 T 细胞上的 CD3 结合。
DR30318 表现出对 CLDN18.2、HSA 和 CD3 的结合亲和力,并在体外显示出 T 细胞依赖性细胞毒性(TDCC)活性。药代动力学分析显示,在啮齿动物中的半衰期为 22.2-28.6 小时,在食蟹猴中为 41.8 小时。在食蟹猴中,DR30318 的给药导致 IL-6 和 C 反应蛋白(CRP)水平略有升高。此外,在与人 PBMC 和表达 CLDN18.2 的细胞孵育后,DR30318 诱导 TDCC 活性和白细胞介素-6(IL-6)和干扰素-γ(IFN-γ)的产生。值得注意的是,DR30318 对胃癌异种移植模型 NUGC4/hCLDN18.2 和胰腺癌异种移植模型 BxPC3/hCLDN18.2 表现出显著的肿瘤抑制作用,而不影响小鼠的体重。