Targeting the Golgi apparatus enhances PD-L1 blockade and synergizes with oxaliplatin to improve immunotherapy efficacy
Haohuan Li·Li Chen·Keren Long·Lu Lu·Shibo Tian·Juan Deng·Long Jin·Jiaxue Cao·Peng Yuan·Qin Zhong·Ziyu Chen·Desheng Li·Xiaolan Fan·Zhiyong Qian·Fanli Kong·Chengdong Wang·Dengfeng Gao·Xiaoxia Liang·Funeng Xu·Chao Cui·Chenglu Sun
Immune checkpoint blockade targeting programmed death ligand-1 (PD-L1) has emerged as a cornerstone of cancer immunotherapy, yielding durable responses in subsets of patients across multiple malignancies. However, clinical outcomes remain limited because of incomplete blockade, low tumor immunogenicity, and poor targeting specificity. Here, we report the development of a chondroitin sulfate-modified liposomal formulation (OPCR-Lip) designed to achieve comprehensive PD-L1 blockade while reprogram
