| Literature DB >> 30444351 |
Guanjun Deng1,2, Zhihong Sun1, Sanpeng Li1,2, Xinghua Peng1,2, Wenjun Li1, Lihua Zhou1, Yifan Ma1, Ping Gong1, Lintao Cai1.
Abstract
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.Entities:
Keywords: M1 macrophages; NK cell membranes; antitumor immunity; cell-membrane immunotherapy; photodynamic therapy
Mesh:
Substances:
Year: 2018 PMID: 30444351 DOI: 10.1021/acsnano.8b05292
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881