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Antitumor activity of Z15-0-2, a bispecific nanobody targeting PD-1 and CTLA-4.
Zeng, Jianyao; Fang, Yuan; Zhang, Zixuan; Lv, Zhenzhen; Wang, Xiaodie; Huang, Qian; Tian, Zhidan; Li, Jiaguo; Xu, Wenfeng; Zhu, Weimin; Yu, Jing; Liu, Tao; Qian, Qijun.
Affiliation
  • Zeng J; School of Medicine, Shanghai University, Shanghai, 200444, China.
  • Fang Y; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Zhang Z; School of Medicine, Shanghai University, Shanghai, 200444, China.
  • Lv Z; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Wang X; School of Medicine, Shanghai University, Shanghai, 200444, China.
  • Huang Q; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Tian Z; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Li J; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Xu W; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Zhu W; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Yu J; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China.
  • Liu T; Shanghai Cell Therapy Group Co., Ltd, Shanghai, 201805, China. liut@shcell.com.
  • Qian Q; School of Medicine, Shanghai University, Shanghai, 200444, China. qianqj@shu.edu.cn.
Oncogene ; 43(29): 2244-2252, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38806619
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antibodies, Bispecific / CTLA-4 Antigen / Programmed Cell Death 1 Receptor / Single-Domain Antibodies Limits: Animals / Female / Humans Language: En Journal: Oncogene Journal subject: BIOLOGIA MOLECULAR / NEOPLASIAS Year: 2024 Document type: Article Affiliation country: China Country of publication: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antibodies, Bispecific / CTLA-4 Antigen / Programmed Cell Death 1 Receptor / Single-Domain Antibodies Limits: Animals / Female / Humans Language: En Journal: Oncogene Journal subject: BIOLOGIA MOLECULAR / NEOPLASIAS Year: 2024 Document type: Article Affiliation country: China Country of publication: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM