声动力疗法
纳米载体
免疫疗法
佐剂
癌症免疫疗法
癌症研究
免疫原性细胞死亡
癌细胞
荧光寿命成像显微镜
化学
免疫系统
光动力疗法
医学
癌症
材料科学
纳米技术
免疫学
药物输送
荧光
内科学
有机化学
物理
量子力学
作者
Yuanyuan Zhang,Yujie Zhang,Yonghong Li,Yuhan Fu,Yuanru Zhao,Wei Zhao,Runqing Li,Yao Xian,Kangsheng Tu,Feng Wu,Cheng Li,Yuzhu Hou,Mingzhen Zhang
标识
DOI:10.1016/j.cej.2023.145685
摘要
The combination of sonodynamic therapy (SDT) with immunotherapy can not only overcome the limitations of immunotherapy such as poor responsiveness and high side effects but also improve the sensitivity of SDT. Here an integrated biomimetic nanoparticle was constructed for NIR-II fluorescence imaging-guided sonodynamic-immune combination therapy. Polymer micelles (Ag2S@P) were synthesized by self-assembly of Ag2S QDs and amphiphilic polymers Pluronic F-127, and the micelles were modified with the homologous adjuvant-embedded cancer cell membrane to generate a biomimetic nanocarriers Ag2S@P@CM-A. The modified cancer cell membrane endowed nanoparticles homologous targeting ability. Under NIR-II fluorescence imaging-guided SDT, Ag2S@P@M-A generates reactive oxygen species (ROS) induced immunogenic cell death (ICD) that is characterized by the release of tumor-associated antigens (TAAs) and damage-associated molecular patterns (DAMPs). Meanwhile, the nanoparticles released toll-like receptor 4 agonist monophosphoryl lipid A (MPLA) in tumors, together with TAAs and DAMPs, to promote dendritic cell (DCs) maturation, cytotoxic T cells activation, and tumor infiltration, effectively inhibiting tumor growth. In combination with checkpoint blockade PD-L1, Ag2S@P@M-A mediated sonodynamic-immunotherapy exhibited more potent anticancer efficacy. In conclusion, our study reported a promising therapeutic strategy for bridging the limitations of SDT and immunotherapy to enhance the efficacy of cancer therapy.
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