声动力疗法
材料科学
免疫疗法
癌症免疫疗法
细菌
癌症
纳米技术
医学
生物
生物化学
内科学
细胞凋亡
遗传学
作者
Cheng Wang,Linfu Chen,Jiafei Zhu,Chunjie Wang,Maoyi Li,Miao Yu,Nanhui Liu,Jiayu Zhao,Feng Pan,Yi Liu,Junjie Zhu,Yang Yang,Qian Chen
标识
DOI:10.1002/adfm.202316092
摘要
Abstract Synthetic biology is propelling medicine into a new era through its capacity to genetically program living cells. One of the particular interests is engineering bacteria as a live and targeted therapeutic delivery system. Herein, the bacterial biohybrid ( E. coli ‐pE@PCN) is developed by genetically engineering Escherichia coli BL21 to overexpress catalase ( E. coli ‐pE) and electrostatically adsorbing nano‐sonosensitizers (PCN NPs) for enhanced and targeted sonodynamic therapy (SDT). Leveraging the ability to colonize and penetrate deep in tumors, engineered bacteria can not only sustainably express catalase to relieve tumor hypoxia, but also facilitate the enriched and expanded distribution of the carried sonosensitizer at the tumor site, so as to trigger effective SDT. More interestingly, it is found that E. coli ‐pE@PCN‐based SDT can successfully inhibit the growth of subcutaneous and orthotopic colorectal tumors by inducing potent antitumor immune responses due to the released tumor‐associated antigens and native immunogenicity of bacterial pathogen‐associated molecular patterns. Furthermore, E. coli ‐pE@PCN‐based SDT can not only prime a strong immune memory response to prevent tumor recurrence but also elicit a potent abscopal effect to inhibit tumor metastasis. Therefore, the programmable bacteria‐based biohybrids developed here pave an avenue to prepare next‐generation sonodynamic‐immunotherapeutics to eliminate cancer and prevent its relapse and metastasis.
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