Photothermal therapy and immunotherapy have attracted widespread attention because of their great advantages for enhancing the effectiveness of cancer treatment and reducing side effects. However, they also have their own shortcomings. Based on the characteristics of photothermal therapy and immunotherapy, functionalized nanoparticle-mediated photothermal-immune synergistic therapy can effectively compensate for their respective deficiencies and produce synergistic effects. Herein, we designed a bioengineering strategy to construct a novel anticancer nanoplatform (AM@DSPE-PEG/OMV) for photothermal-immunotherapy of cancer by coating bacterial outer membrane vesicles onto polyethylene glycolized antimony alkene nanosheets (AM@DSPE-PEG). Bacterial outer membrane vesicles (OMV) have emerged as potent activators of the host immune response in the realm of cancer immunotherapy. In conjunction with near-infrared light irradiation, antimonene nanosheets demonstrate remarkable photothermal properties, thereby instigating immunogenic cell death and facilitating the release of both antigens and "danger signals". This dual mechanism facilitates the thermal ablation of primary tumors, thereby eliciting an immune response. Additionally, these processes further stimulate the maturation of dendritic cells, consequently augmenting antigen presentation and fortifying the immune response. Thus, the synergistic utilization of OMV and antimonene nanosheets holds promise in enhancing the efficacy of immunotherapeutic interventions for cancer. We demonstrated that AM@DSPE-PEG/OMV can passively target tumors, exhibit excellent biocompatibility and superior photothermal conversion efficiency, significantly upregulate the secretion levels of cellular pro-inflammatory factors, and display outstanding cytotoxic effects against cancer cells in vitro. In summary, this bioengineering strategy displayed a broader prospect for photothermal-immunotherapy synergy.
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