Core-shell nanoscale coordination polymers combine chemotherapy and photodynamic therapy to potentiate checkpoint blockade cancer immunotherapy

被引:784
作者
He, Chunbai [1 ]
Duan, Xiaopin [1 ]
Guo, Nining [1 ,2 ,3 ]
Chan, Christina [1 ]
Poon, Christopher [1 ]
Weichselbaum, Ralph R. [2 ,3 ]
Lin, Wenbin [1 ]
机构
[1] Univ Chicago, Dept Chem, 929 E 57th St, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Radiat & Cellular Oncol, 5758 S Maryland Ave, Chicago, IL 60637 USA
[3] Univ Chicago, Ludwig Ctr Metastasis Res, 5758 S Maryland Ave, Chicago, IL 60637 USA
关键词
IMMUNE-SYSTEM; CELL-DEATH; TUMOR; PD-1; MICROENVIRONMENT; NANOPARTICLES; ANTIBODIES; TOLERANCE; MELANOMA; PATHWAY;
D O I
10.1038/ncomms12499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Advanced colorectal cancer is one of the deadliest cancers, with a 5-year survival rate of only 12% for patients with the metastatic disease. Checkpoint inhibitors, such as the antibodies inhibiting the PD-1/PD-L1 axis, are among the most promising immunotherapies for patients with advanced colon cancer, but their durable response rate remains low. We herein report the use of immunogenic nanoparticles to augment the antitumour efficacy of PD-L1 antibody-mediated cancer immunotherapy. Nanoscale coordination polymer (NCP) core-shell nanoparticles carry oxaliplatin in the core and the photosensitizer pyropheophorbide-lipid conjugate (pyrolipid) in the shell (NCP@pyrolipid) for effective chemotherapy and photodynamic therapy (PDT). Synergy between oxaliplatin and pyrolipid-induced PDT kills tumour cells and provokes an immune response, resulting in calreticulin exposure on the cell surface, antitumour vaccination and an abscopal effect. When combined with anti-PD-L1 therapy, NCP@pyrolipid mediates regression of both light-irradiated primary tumours and non-irradiated distant tumours by inducing a strong tumour-specific immune response.
引用
收藏
页数:12
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