免疫原性细胞死亡
癌症研究
免疫系统
先天免疫系统
免疫
生物
免疫疗法
材料科学
免疫学
作者
Zhen Ya,Hai‐Tao Wu,Wanlin Jia,Hanbing Chu,Mingting Zhu,Yan Li,Lei Zhang,Yujin Zong,Shifang Guo,Mingxi Wan
出处
期刊:Small
[Wiley]
日期:2025-06-08
卷期号:21 (30)
标识
DOI:10.1002/smll.202503639
摘要
Abstract Engineered bacteria as intelligent microbots preferentially targeting and colonizing tumors have overcome the poor delivery efficacy of nanomedicines toward large hypoxic tumors. In this study, Escherichia coli ( E.coli ) filled with gas vesicles is modified with drugs‐loaded liposomes via amide condensation to achieve synergistic sono‐chemotherapy. In this study, to regulate intelligent microbots for high‐performance tumor therapy, a whirlwind‐focused acoustic vortex (FAV) is used, which has a larger focal region and stronger thermal and cavitation effects as compared to the conventional focused ultrasound (FUS). The large tumors receiving single FAV irradiation exhibited enhanced and uniform drug bioaccumulation throughout the entire tumor due to the full coverage and rapid and uniform heating characteristics of FAV irradiation. The FAV‐regulated intelligent microbots caused more serious DNA double‐strand breaks (DSBs), activated the cyclic GMP‐AMP synthase‐stimulator of interferon genes (cGAS‐STING) pathway to release immune cytokines, and induced immunogenic cell death (ICD) for innate immunity activation. The activated systemic immunity is further boosted by combining FAV‐regulated sono‐chemotherapy with immune checkpoint blockades to increase the infiltration of cytotoxic T cells, decrease the population of immunosuppressive cells, and finally reshape the immunosuppressive tumor microenvironment. This study provides a synergistic strategy via regulating intelligent microbots for large tumor immunotherapy.
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