A Three-in-One Nanoscale Coordination Polymer for Potent Chemo-Immunotherapy

被引:11
|
作者
Liu, Jing [1 ,2 ,3 ]
Jiang, Xiaomin [1 ]
Feng, Xuanyu [1 ]
Lee, Morten J. [1 ]
Li, Youyou [1 ]
Mao, Jianming [1 ]
Weichselbaum, Ralph R. [2 ,3 ]
Lin, Wenbin [1 ,2 ,3 ]
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
[3] Univ Chicago, Ludwig Ctr Metastasis Res, Chicago, IL 60637 USA
关键词
chemotherapy; immunogenic cell death; immunotherapy; nanoscale coordination polymers; programmed cell death-ligand 1; IMMUNOGENIC CELL-DEATH; COMBINATION THERAPY; CO-DELIVERY; OPEN-LABEL; CANCER; CHEMOTHERAPY; BLOCKADE; ANTIBODY; PD-L1; ADENOCARCINOMA;
D O I
10.1002/smtd.202201437
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The addition of immune checkpoint blockade to standard chemotherapy has changed the standards of care for some cancer patients. However, current chemo-immunotherapy strategies do not benefit most colorectal cancer patients and many triple-negative breast cancer patients. Here, the design of a three-in-one nanoscale coordination polymer (NCP), OX/GC/CQ, comprising prodrugs of oxaliplatin (OX), gemcitabine (GC), and 5-carboxy-8-hydroxyquinoline (CQ) for triple-modality chemo-immunotherapy is reported. OX/GC/CQ exhibits optimal pharmacokinetics and enhanced particle accumulation and drug release in acidic tumor tissues, wherein CQ greatly enhances immunogenic cell death induced by OX/GC and down-regulates programmed cell death-ligand 1 expression in cancer cells. Consequently, OX/GC/CQ efficiently promotes infiltration and activity of cytotoxic T lymphocytes, while decreasing the proportion of immunosuppressive regulatory T cells. Intravenous injection of OX/GC/CQ reduces the growth of colorectal carcinoma and triple-negative breast cancer, prevents metastasis to lungs, and extends mouse survival by 30-40 days compared to free drugs. This work highlights the potential of NCPs in co-delivering synergistic chemo-immunotherapeutics for the treatment of advanced and aggressive cancers.
引用
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页数:13
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