首页|靶向PD-1/PD-L1的新策略:降解剂、双功能分子及共价抑制剂

靶向PD-1/PD-L1的新策略:降解剂、双功能分子及共价抑制剂

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靶向细胞程序性死亡受体-1(programmed cell death protein-1,PD-1)/细胞程序性死亡配体-1(programmed cell death ligand-1,PD-L1)已成为最具前景的肿瘤免疫治疗靶点之一.目前,PD-1/PD-L1单克隆抗体药物及小分子抑制剂都面临着相应的发展瓶颈,许多研究者尝试探索不同的策略以阻断PD-L1/PD-L1通路,期望改善肿瘤治疗的效果.本文总结了靶向PD-L1的降解剂、双功能分子及共价抑制剂,旨在为PD-1/PD-L1药物的开发提供有益的思路.
New strategies for targeting PD-1/PD-L1:degraders,bifunctional molecules and covalent inhibitors
Programmed cell death protein-1(PD-1)/programmed cell death ligand-1(PD-L1)has been considered to be one of the most promising targets for tumor immunotherapy.At present,both monoclonal antibody drugs and small molecule inhibitors targeting PD-1/PD-L1 are facing bottlenecks.Numerous researchers have tried to explore different strategies to block the PD-L1/PD-L1 pathway,hoping to improve the effects of tumor immunotherapy.This review focuses on the degraders,bifunctional molecules and covalent inhibitors that target PD-L1,aiming to provide inspiring insights for the development of anti-PD-1/PD-L1 drugs.

PD-1/PD-L1tumor immunotherapydegradersbifunctional moleculescovalent inhibitors

王志杰、廖晓彤、郭霞、陈建军

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南方医科大学深圳医院, 深圳 518100

南方医科大学药学院, 广州 510515

PD-1/PD-L1 肿瘤免疫 降解剂 双功能分子 共价抑制剂

国家自然科学基金国家自然科学基金

8217366882373706

2024

中国药科大学学报
中国药科大学

中国药科大学学报

CSTPCD北大核心
影响因子:0.655
ISSN:1000-5048
年,卷(期):2024.55(1)
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