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Cell-Membrane Immunotherapy Based on Natural Killer Cell Membrane Coated Nanoparticles for the Effective Inhibition of Primary and Abscopal Tumor Growth
404
Citations
23
References
2018
Year
NanoparticlesNanotherapeuticsEngineeringImmunologyImmunoeditingImmunotherapeuticsImmunotherapyNatural Killer CellsTumor BiologyNk Cell MembranesNanomedicineTumor ImmunologyTumor ImmunityShotgun ProteomicsRadiation OncologyTherapeutic VaccineTumor TargetingNatural KillerCell-membrane ImmunotherapyEffective InhibitionCell BiologyTumor MicroenvironmentCancer ImmunosurveillanceImmune Checkpoint InhibitorNano-drug DeliveryMedicineAbscopal Tumor Growth
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.
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