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携带基于多酚的超微粒的口服纳米装甲活细菌生物疗法通过重建免疫肿瘤学-微生物群轴增强化疗效果。

Oral Nanoarmored Live Bacterial Biotherapeutics Bearing Polyphenol-Based Supraparticles Enhance Chemotherapy via Reestablishing Immuno-Oncology-Microbiome Axis.

作者信息

Liu Qinling, Wu Yue, Fan Qingxin, Liu Jialing, Chen Yan, He Yuanmeng, Wei Wenqi, Zhang Haojie, Zhao Yueling, He Yunxiang, Du Xiao, Guo Junling

机构信息

Tea Resources Utilization and Quality Testing Key Laboratory of Sichuan Province, College of Horticulture, Sichuan Agricultural University, Chengdu, Sichuan 611130, China.

BMI Center for Biomass Materials and Nanointerfaces, National Engineering Laboratory for Clean Technology of Leather Manufacture, Ministry of Education Key Laboratory of Leather Chemistry and Engineering, College of Biomass Science and Engineering, Sichuan University, Chengdu, Sichuan 610065, China.

出版信息

ACS Nano. 2025 Jul 8;19(26):23575-23591. doi: 10.1021/acsnano.5c01158. Epub 2025 Jun 26.

Abstract

The immuno-oncology-microbiome (IOM) axis, referring to the gut microbiota-regulated immune interactions on the tumor microenvironment and systemic immunity, is essential for cancer therapies. However, the cytotoxicity of chemotherapeutic agents (Chemos) disrupts the gut microbiota- and gut microbiota-manipulated IOM axis, further diminishing the therapeutic efficacy. Here, we developed oral nanoarmored live bacterial biotherapeutics (supraLBT), to reshape the tumor microenvironment and enhance chemotherapy via reestablishing the IOM axis. The cyto-adhesive polyphenol-based supraparticles, made from green tea polyphenol and food-grade milk protein, attached on microbes ( Nissle1917, EcN) resisted a range of clinically relevant Chemos via phenolic-mediated noncovalent interactions, enhancing supraLBT survival by 27-fold compared with bare EcN. SupraLBT restored the intestinal microbiota and the disrupted IOM axis, thereby reducing the infiltration of regulatory T cells, increasing the recruitment of cytotoxic CD8 T cells to the tumor bed, and further inhibiting tumor proliferation and demonstrating enhanced systemic immune responses. Notably, oral supraLBT combined with chemotherapy (doxorubicin) exhibited 2.35-fold greater tumor regression than that of doxorubicin alone, indicating that oral supraLBT can enhance the chemotherapeutic effect. Further investigations revealed that supraLBT reprogrammed the immune tumor microenvironment by upregulating antitumor cytokines and altering the gut microbial composition. Given the intricate interplay between gut microbiota, host immune system, and tumor microenvironment, this work presents a facile and biomaterial-engineered microorganism-based strategy to enhance the synergistic immuno-chemotherapy effects.

摘要

免疫肿瘤学-微生物群(IOM)轴,指的是肠道微生物群对肿瘤微环境和全身免疫的调节性免疫相互作用,对癌症治疗至关重要。然而,化疗药物(Chemos)的细胞毒性会破坏肠道微生物群以及由肠道微生物群操控的IOM轴,进而降低治疗效果。在此,我们开发了口服纳米装甲活细菌生物疗法(supraLBT),通过重建IOM轴来重塑肿瘤微环境并增强化疗效果。由绿茶多酚和食品级乳蛋白制成的基于细胞粘附多酚的超微粒附着在微生物(Nissle1917、EcN)上,通过酚介导的非共价相互作用抵抗一系列临床相关的化疗药物,与裸露的EcN相比,使supraLBT的存活率提高了27倍。SupraLBT恢复了肠道微生物群和被破坏的IOM轴,从而减少调节性T细胞的浸润,增加细胞毒性CD8 T细胞向肿瘤床的募集,并进一步抑制肿瘤增殖,同时表现出增强的全身免疫反应。值得注意的是,口服supraLBT联合化疗(阿霉素)显示出的肿瘤消退效果比单独使用阿霉素高2.35倍,表明口服supraLBT可增强化疗效果。进一步研究表明,supraLBT通过上调抗肿瘤细胞因子和改变肠道微生物组成来重新编程免疫肿瘤微环境。鉴于肠道微生物群、宿主免疫系统和肿瘤微环境之间复杂的相互作用,这项工作提出了一种简便的、基于生物材料工程微生物的策略,以增强免疫化疗的协同效果。

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