Aggregation-induced emission photosensitizer/bacteria biohybrids enhance Cerenkov radiation-induced photodynamic therapy by activating anti-tumor immunity for synergistic tumor treatment

被引:17
|
作者
Zhu, Ziyang [1 ,2 ,3 ]
Liu, Qingyao [1 ,2 ,3 ]
Zhu, Ke
Wang, Kun [4 ,5 ]
Lin, Lan [6 ]
Chen, Yaqi [7 ]
Shao, Fuqiang [4 ]
Qian, Ruijie [1 ,2 ,3 ]
Song, Yangmeihui [1 ,2 ,3 ]
Gao, Yu [1 ,2 ,3 ]
Yang, Biao [1 ,2 ,3 ]
Jiang, Dawei [1 ,2 ,3 ]
Lan, Xiaoli [1 ,2 ,3 ]
An, Rui [1 ,2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Nucl Med, Wuhan 430022, Peoples R China
[2] Hubei Prov Key Lab Mol Imaging, Wuhan 430022, Peoples R China
[3] Minist Educ, Key Lab Biol Targeted Therapy, Wuhan 430022, Peoples R China
[4] Zigong Acad Med Sci, Zigong First Peoples Hosp, Dept Nucl Med, Zigong 643000, Peoples R China
[5] Tongji Univ, Shanghai East Hosp, Sch Med, Dept Nucl Med, Shanghai 200120, Peoples R China
[6] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Integrated Tradit Chinese & Western Med, 1277 Jiefang Ave, Wuhan 430022, Peoples R China
[7] Huazhong Univ Sci & Technol, Liyuan Hosp, Tongji Med Coll, Wuhan 430077, Peoples R China
关键词
Bacteria; Cerenkov radiation; Photodynamic therapy; Tumor immunotherapy; Biohybrids; IMMUNOGENIC CELL-DEATH; SALMONELLA-TYPHIMURIUM;
D O I
10.1016/j.actbio.2023.06.009
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cerenkov radiation-induced photodynamic therapy (CR-PDT) gets rid of the limited tissue penetration depth of the external light source and provides a feasible scheme for the PDT excited by the internal light. However, due to the low luminescence intensity of Cerenkov radiation, CR-PDT alone cannot effectively inhibit tumor growth, curbing the potential clinical translation of CR-PDT. Herein, we reported an AIE-PS/bacteria biohybrid (EcN@TTVP) composed of Escherichia coli Nissle 1917 (EcN) loaded with aggregation-induced emission photosensitizer (AIE-PS) termed TTVP, which enhanced CR-PDT by activating anti-tumor immunity for synergistic tumor treatment. The preferential tumor-colonized EcN@TTVP and radiopharmaceutical 18 F-fluorodeoxyglucose ( 18 F-FDG) were administered sequentially to enable them to co-enrich in the tumor site, thereby triggering CR-PDT and promoting immunogenic tumor cell death. Most importantly, EcN acting as immunoadjuvants enhanced the maturation of dendritic cells (DCs) and priming of cytotoxic T cells (CTLs). Therefore, under the synergistic treatment of CR-PDT and immunotherapy, AIE-PS/bacteria biohybrids resulted in either efficient tumor remission or a survival prolongation in tumor-bearing mice, which presented significant advantages over single CR-PDT. Remarkably, no obvious toxic effects were observed during the treatment. In this study, we proposed a synergistic therapeutic strategy based on EcN@TTVP for combined CR-PDT and immunotherapy against tumors. Moreover, this strategy may have great potential in clinical translation and provide references for deep-seated tumor treatment.
引用
收藏
页码:519 / 533
页数:15
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