Cell-Membrane Immunotherapy Based on Natural Killer Cell Membrane Coated Nanoparticles for the Effective Inhibition of Primary and Abscopal Tumor Growth

被引:335
作者
Deng, Guanjun [1 ,2 ]
Sun, Zhihong [1 ]
Li, Sanpeng [1 ,2 ]
Peng, Xinghua [1 ,2 ]
Li, Wenjun [1 ]
Zhou, Lihua [1 ]
Ma, Yifan [1 ]
Gong, Ping [1 ]
Cai, Lintao [1 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, CAS HK Joint Lab Biomat,CAS Key Lab Hlth Informat, Guangdong Key Lab Nanomed,Shenzhen Engn Lab Nanom, Shenzhen 518055, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
cell-membrane immunotherapy; NK cell membranes; M1; macrophages; photodynamic therapy; antitumor immunity; PHOTODYNAMIC THERAPY; T-CELLS; BLOCKADE; CYTOTOXICITY; POLARIZATION; RECOGNITION; M1;
D O I
10.1021/acsnano.8b05292
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing effective immunotherapies with low toxicity and high tumor specificity is the ultimate goal in the battle against cancer. Here, we reported a cell-membrane immunotherapy strategy that was able to eliminate primary tumors and inhibited distant tumors by using natural killer (NK) cell membrane cloaked photosensitizer 4,4',4 '',4"'-(porphine-5,10,15,20-tetrayl) tetrakis (benzoic acid) (TCPP)-loaded nanoparticles (NK-NPs). The proteomic profiling of NK cell membranes was performed through shotgun proteomics, and we found that NK cell membranes enabled the NK-NPs to target tumors and could induce or enhance pro-inflammatory M1-macrophages polarization to produce antitumor immunity. The TCPP loaded in NK-NPs could induce cancer cell death through photodynamic therapy and consequently enhanced the antitumor immunity efficiency of the NK cell membranes. The results confirmed that NK-NPs selectively accumulated in the tumor and were able to eliminate primary tumor growth and produce an abscopal effect to inhibit distant tumors. This cell-membrane immunotherapeutic approach offers a strategy for tumor immunotherapy.
引用
收藏
页码:12096 / 12108
页数:13
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