生物
细胞毒性T细胞
癌症研究
信使核糖核酸
抗原
体内
抗体
体外
双特异性抗体
分子生物学
免疫学
单克隆抗体
基因
生物化学
遗传学
作者
J Zeng,Yuan Fang,Zixuan Zhang,Zhenzhen Lv,Xiaodie Wang,Qian Huang,Zhidan Tian,Jiaguo Li,Wenfeng Xu,Weimin Zhu,Jing Yu,Tao Liu,Qijun Qian
出处
期刊:Oncogene
[Springer Nature]
日期:2024-05-28
卷期号:43 (29): 2244-2252
被引量:4
标识
DOI:10.1038/s41388-024-03066-5
摘要
Abstract 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.
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