School of Medicine, Shanghai University, Shanghai, 200444, China.
Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
Oncogene. 2024 Jul;43(29):2244-2252. doi: 10.1038/s41388-024-03066-5. Epub 2024 May 28.
The combination of programmed cell death protein 1 (PD-1) and cytotoxic T lymphocyte antigen 4 (CTLA-4) antibodies has potential for enhancing clinical efficacy. We described the development and antitumor activity of Z15-0, a bispecific nanobody targeting both the PD-1 and CTLA-4 pathways simultaneously. We designed and optimized the mRNA sequence encoding Z15-0, referred to as Z15-0-2 and through a series of in vitro and in vivo experiments, we established that the optimized Z15-0-2 mRNA sequence significantly increased the expression of the bispecific nanobody. Administration of Z15-0-2 mRNA to tumor-bearing mice led to greater inhibition of tumor growth compared to controls. In aggregate, we introduced a novel bispecific nanobody and have re-engineered it to boost expression of mRNA, representing a new drug development paradigm.
程序性死亡蛋白 1(PD-1)和细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)抗体的联合应用具有增强临床疗效的潜力。我们描述了 Z15-0 的开发和抗肿瘤活性,Z15-0 是一种同时针对 PD-1 和 CTLA-4 途径的双特异性纳米抗体。我们设计并优化了编码 Z15-0 的 mRNA 序列,称为 Z15-0-2,并通过一系列体外和体内实验,我们确定了优化的 Z15-0-2 mRNA 序列显著增加了双特异性纳米抗体的表达。与对照组相比,向荷瘤小鼠给予 Z15-0-2 mRNA 可导致更大程度的肿瘤生长抑制。总之,我们引入了一种新型的双特异性纳米抗体,并对其进行了重新设计以提高 mRNA 的表达,这代表了一种新的药物开发范例。