免疫疗法
封锁
内化
适体
PD-L1
癌症免疫疗法
癌症研究
化学
免疫检查点
嵌合体(遗传学)
基因沉默
融合蛋白
免疫系统
细胞
生物
受体
免疫学
分子生物学
生物化学
重组DNA
基因
作者
Fatao Luo,Gang Yang,Xia Bai,Deyu Yuan,Ling Li,Diyue Wang,LU Xiao-xiang,Yiran Cheng,Yuchun Wang,Xu Song,Yongyun Zhao
标识
DOI:10.1016/j.chembiol.2023.10.010
摘要
Checkpoint inhibitor antibody therapy by blocking the interaction of surface programmed death-ligand 1(PD-L1) and programmed cell death protein 1(PD-1) has promising advantages in cancer immunotherapy. However, the response of many patients remains unsatisfactorily, suspected to be relevant to PD-L1 located in other cellular compartments and antibodies do not have access to the intracellular compartments. Herein, we identify a PD-L1-targeting DNA aptamer (PA9-1) with dual roles, including an antagonist and a delivery agent dependent on PD-L1 internalization. And we design the PD-L1-targeting antagonistic aptamer-ASO delivery system (PA9-1-ASO), with synergistic inhibitory PD-L1 activity involving the combination of blockade and silencing mechanisms. This chimera not only blocks PD-L1/PD-1 but also achieves targeted delivery of the conjugated ASO to reduce both surface PD-L1 and total PD-L1 expression. Compared with the single blockade, this chimera with the dual inhibitory function synergistically inhibits PD-L1 to amplify immunotherapeutic efficacy, providing a promising synergistic strategy for immunotherapy.
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