Key Laboratory of Medical Imaging Precision Theranostics and Radiation Protection, University of South China, College of Hunan Province, Changsha, Hunan 410028, China; Institution of Medical Imaging, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, China; CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Cell Rep Med. 2024 May 21;5(5):101512. doi: 10.1016/j.xcrm.2024.101512. Epub 2024 Apr 18.
Our previous work developed acoustic response bacteria, which enable the precise tuning of transgene expression through ultrasound. However, it is still difficult to visualize these bacteria in order to guide the sound wave to precisely irradiate them. Here, we develop ultrasound-visible engineered bacteria and chemically modify them with doxorubicin (DOX) on their surfaces. These engineered bacteria (Ec@DIG-GVs) can produce gas vesicles (GVs), providing a real-time imaging guide for remote hyperthermia high-intensity focused ultrasound (hHIFU) to induce the expression of the interferon (IFN)-γ gene. The production of IFN-γ can kill tumor cells, induce macrophage polarization from the M2 to the M1 phenotype, and promote the maturation of dendritic cells. DOX can be released in the acidic tumor microenvironment, resulting in immunogenic cell death of tumor cells. The concurrent effects of IFN-γ and DOX activate a tumor-specific T cell response, producing the synergistic anti-tumor efficacy. Our study provides a promising strategy for bacteria-mediated tumor chemo-immunotherapy.
我们之前的工作开发了声响应细菌,通过超声波实现转基因表达的精确调节。然而,要对这些细菌进行可视化仍然很困难,以便引导声波精确照射它们。在这里,我们开发了超声可见的工程细菌,并在其表面用阿霉素(DOX)对其进行化学修饰。这些工程细菌(Ec@DIG-GVs)可以产生气穴(GVs),为远程高热高强度聚焦超声(hHIFU)诱导干扰素(IFN)-γ基因的表达提供实时成像指导。IFN-γ 的产生可以杀死肿瘤细胞,诱导巨噬细胞从 M2 向 M1 表型极化,并促进树突状细胞的成熟。DOX 可以在酸性肿瘤微环境中释放,导致肿瘤细胞发生免疫原性细胞死亡。IFN-γ 和 DOX 的协同作用激活了肿瘤特异性 T 细胞反应,产生了协同的抗肿瘤疗效。我们的研究为细菌介导的肿瘤化疗免疫治疗提供了一种很有前途的策略。