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用于靶向肿瘤定植和局部治疗递送的自调节工程益生菌

Self-Adjusting Engineered Probiotic for Targeted Tumor Colonization and Local Therapeutics Delivery.

作者信息

Zou Zhen-Ping, Wang Xin-Ge, Shi Xuan-Ren, Sun Shu-Ting, Mi Jing, Zhang Xiao-Peng, Yin Bin-Cheng, Zhou Ying, Ye Bang-Ce

机构信息

Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.

Institute of Engineering Biology and Health, Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.

出版信息

Adv Sci (Weinh). 2025 Aug;12(31):e06486. doi: 10.1002/advs.202406486. Epub 2025 May 28.

DOI:10.1002/advs.202406486
PMID:40432606
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12376540/
Abstract

Engineered bacteria have demonstrated great potential for treating a broad array of tumors. However, the precision and safety of controlling the performance of engineered bacteria in vivo remains a central challenge. Here, genetic circuit programming strategy is utilized to construct an engineered Escherichia coli Nissle 1917 with accurate targeted colonizing and on-demand payloads releasing ability. The engineered probiotic survives only in the presence of more than 5 mM L-lactate by employing an improved lactate-sensing system, which leads to preventing the growth outside the permissive environments in mice. Meanwhile an expressing α-hemolysin (SAH) circuit based on quorum-sensing system is introduced to augment anti-tumor effect. Furthermore, coagulase (Coa) induced by high-level lactate creates the closure to deprive tumor of nutrients and oxygen and may help prevent the leakage of bacteria and SAH, which enhances the therapeutic effectiveness and biosafety. This self-adjusting living biotherapeutics significantly inhibits tumor proliferation and prolongs the survival time of colorectal tumor-bearing mice. Together, this work takes a step toward safer and more effective application of living bacteria for tumor treatment in practice.

摘要

工程菌已显示出在治疗多种肿瘤方面的巨大潜力。然而,在体内控制工程菌性能的精确性和安全性仍然是一个核心挑战。在此,利用基因回路编程策略构建了一种具有精确靶向定殖和按需释放载荷能力的工程化大肠杆菌Nissle 1917。通过采用改进的乳酸感应系统,工程益生菌仅在存在超过5 mM L-乳酸的情况下存活,这导致其在小鼠体内的允许环境之外无法生长。同时,引入基于群体感应系统的表达α-溶血素(SAH)回路以增强抗肿瘤效果。此外,由高水平乳酸诱导的凝固酶形成封闭,剥夺肿瘤的营养和氧气,并可能有助于防止细菌和SAH泄漏,从而提高治疗效果和生物安全性。这种自我调节的活体生物疗法显著抑制肿瘤增殖并延长结直肠癌荷瘤小鼠的存活时间。总之,这项工作朝着在实践中更安全、更有效地应用活菌进行肿瘤治疗迈出了一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/c54204cce1dd/ADVS-12-e06486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/f8450bd68f13/ADVS-12-e06486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/da5158844ef8/ADVS-12-e06486-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/0e6dfe25a44f/ADVS-12-e06486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/4753c4960125/ADVS-12-e06486-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/e26559e5afd0/ADVS-12-e06486-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/3f34bf76e936/ADVS-12-e06486-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/80d94bc69f04/ADVS-12-e06486-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/c54204cce1dd/ADVS-12-e06486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/f8450bd68f13/ADVS-12-e06486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/da5158844ef8/ADVS-12-e06486-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/0e6dfe25a44f/ADVS-12-e06486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/4753c4960125/ADVS-12-e06486-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/e26559e5afd0/ADVS-12-e06486-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/3f34bf76e936/ADVS-12-e06486-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/80d94bc69f04/ADVS-12-e06486-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adaa/12376540/c54204cce1dd/ADVS-12-e06486-g001.jpg

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本文引用的文献

1
Setting "cold" tumors on fire: Cancer therapy with live tumor-targeting bacteria.点燃“冷”肿瘤:利用靶向肿瘤的活菌进行癌症治疗
Med. 2025 Jan 10;6(1):100549. doi: 10.1016/j.medj.2024.11.002. Epub 2024 Dec 16.
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Probiotic neoantigen delivery vectors for precision cancer immunotherapy.益生菌新抗原递呈载体用于精准癌症免疫治疗。
Nature. 2024 Nov;635(8038):453-461. doi: 10.1038/s41586-024-08033-4. Epub 2024 Oct 16.
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Reprogramming the tumor immune microenvironment using engineered dual-drug loaded Salmonella.利用工程化双重载药沙门氏菌重编程肿瘤免疫微环境。
Nat Commun. 2024 Aug 6;15(1):6680. doi: 10.1038/s41467-024-50950-5.
4
Exploiting bacteria for cancer immunotherapy.利用细菌进行癌症免疫疗法。
Nat Rev Clin Oncol. 2024 Aug;21(8):569-589. doi: 10.1038/s41571-024-00908-9. Epub 2024 Jun 5.
5
Probiotic-guided CAR-T cells for solid tumor targeting.益生菌引导的 CAR-T 细胞用于实体瘤靶向治疗。
Science. 2023 Oct 13;382(6667):211-218. doi: 10.1126/science.add7034. Epub 2023 Oct 12.
6
Protocol for engineering E. coli Nissle 1917 to diagnose, record, and ameliorate inflammatory bowel disease in mice.工程改造大肠杆菌Nissle 1917以诊断、记录和改善小鼠炎症性肠病的方案。
STAR Protoc. 2023 Apr 26;4(2):102254. doi: 10.1016/j.xpro.2023.102254.
7
Active recruitment of anti-PD-1-conjugated platelets through tumor-selective thrombosis for enhanced anticancer immunotherapy.通过肿瘤选择性血栓形成主动募集抗 PD-1 偶联血小板以增强抗癌免疫治疗。
Sci Adv. 2023 Mar 29;9(13):eadf6854. doi: 10.1126/sciadv.adf6854.
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Synthetic bacterial therapies for intestinal diseases based on quorum-sensing circuits.基于群体感应回路的肠道疾病合成细菌疗法。
Biotechnol Adv. 2023 Jul-Aug;65:108142. doi: 10.1016/j.biotechadv.2023.108142. Epub 2023 Mar 26.
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Chemokines expressed by engineered bacteria recruit and orchestrate antitumor immunity.工程菌表达的趋化因子募集并协调抗肿瘤免疫。
Sci Adv. 2023 Mar 10;9(10):eadc9436. doi: 10.1126/sciadv.adc9436. Epub 2023 Mar 8.
10
Biomarker-responsive engineered probiotic diagnoses, records, and ameliorates inflammatory bowel disease in mice.生物标志物响应型工程益生菌诊断、记录并改善小鼠的炎症性肠病。
Cell Host Microbe. 2023 Feb 8;31(2):199-212.e5. doi: 10.1016/j.chom.2022.12.004. Epub 2022 Dec 27.