Engineering tumor-colonizing E. coli Nissle 1917 for detection and treatment of colorectal neoplasia

医学 结直肠癌 益生菌 腺瘤 结直肠腺瘤 临床试验 内科学 癌症 生物 遗传学 细菌
作者
Candice R. Gurbatri,Georgette Radford,Laura Vrbanac,Jongwon Im,E Thomas,Courtney Coker,Samuel Taylor,YoungUk Jang,Ayelet Sivan,Kyu Y. Rhee,Anas A. Saleh,Tiffany Chien,Fereshteh Zandkarimi,Ioana Lia,Tamsin R.M. Lannagan,Tongtong Wang,Josephine A. Wright,Hiroki Kobayashi,Jia Q. Ng,Matt Lawrence,Tarik Sammour,Michelle Thomas,Mark Lewis,Lito E. Papanicolas,Joanne Perry,Tracy Fitzsimmons,Patricia Kaazan,Amanda Lim,Alexandra M. Stavropoulos,Dion A. Gouskos,Julie Marker,Cheri Ostroff,Geraint B. Rogers,Nicholas Arpaia,Daniel L. Worthley,Susan L. Woods,Tal Danino
出处
期刊:Nature Communications [Nature Portfolio]
卷期号:15 (1) 被引量:35
标识
DOI:10.1038/s41467-024-44776-4
摘要

Abstract Bioengineered probiotics enable new opportunities to improve colorectal cancer (CRC) screening, prevention and treatment. Here, first, we demonstrate selective colonization of colorectal adenomas after oral delivery of probiotic E. coli Nissle 1917 (EcN) to a genetically-engineered murine model of CRC predisposition and orthotopic models of CRC. We next undertake an interventional, double-blind, dual-centre, prospective clinical trial, in which CRC patients take either placebo or EcN for two weeks prior to resection of neoplastic and adjacent normal colorectal tissue (ACTRN12619000210178). We detect enrichment of EcN in tumor samples over normal tissue from probiotic-treated patients (primary outcome of the trial). Next, we develop early CRC intervention strategies. To detect lesions, we engineer EcN to produce a small molecule, salicylate. Oral delivery of this strain results in increased levels of salicylate in the urine of adenoma-bearing mice, in comparison to healthy controls. To assess therapeutic potential, we engineer EcN to locally release a cytokine, GM-CSF, and blocking nanobodies against PD-L1 and CTLA-4 at the neoplastic site, and demonstrate that oral delivery of this strain reduces adenoma burden by ~50%. Together, these results support the use of EcN as an orally-deliverable platform to detect disease and treat CRC through the production of screening and therapeutic molecules.
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