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

被引:0
|
作者
Candice R. Gurbatri
Georgette A. Radford
Laura Vrbanac
Jongwon Im
Elaine M. Thomas
Courtney Coker
Samuel R. Taylor
YoungUk Jang
Ayelet Sivan
Kyu 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 Papanicolas
Joanne Perry
Tracy Fitzsimmons
Patricia Kaazan
Amanda Lim
Alexandra M. Stavropoulos
Dion A. Gouskos
Julie Marker
Cheri Ostroff
Geraint Rogers
Nicholas Arpaia
Daniel L. Worthley
Susan L. Woods
Tal Danino
机构
[1] Columbia University,Department of Biomedical Engineering
[2] University of Adelaide,Adelaide Medical School
[3] Weill Cornell-Rockefeller-Sloan Kettering Tri-Institutional MD-PhD program,Division of Infectious Diseases, Weill Department of Medicine
[4] Weill Cornell Medicine,Department of Chemistry
[5] Columbia University,Colorectal Unit, Department of Surgery
[6] South Australian Health and Medical Research Institute (SAHMRI),College of Medicine and Public Health
[7] Royal Adelaide Hospital,Department of Microbiology & Immunology
[8] Flinders University,Herbert Irving Comprehensive Cancer Center
[9] Cancer Voices SA,Data Science Institute
[10] University of South Australia,undefined
[11] Vagelos College of Physicians and Surgeons of Columbia University,undefined
[12] Columbia University,undefined
[13] Colonoscopy Clinic,undefined
[14] Columbia University,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
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.
引用
收藏
相关论文
共 50 条
  • [21] A modified MacConkey agar for selective enumeration of necrotoxigenic E. coli O55 and probiotic E. coli Nissle 1917
    Splichalova, Alla
    Splichal, Igor
    Sonnenborn, Ulrich
    Rada, Vojtech
    JOURNAL OF MICROBIOLOGICAL METHODS, 2014, 104 : 82 - 86
  • [22] The Probiotic E. coli strain Nissle 1917 for the treatment of collagenous colitis:: First results of an open labeled trial
    Tromm, A
    Khoury, M
    Baestlein, E
    Wilhelms, G
    Stolte, M
    GASTROENTEROLOGY, 2003, 124 (04) : A479 - A479
  • [23] E. coli Nissle 1917 Affects Salmonella Adhesion to Porcine Intestinal Epithelial Cells
    Schierack, Peter
    Kleta, Sylvia
    Tedin, Karsten
    Babila, Julius Tachu
    Oswald, Sibylle
    Oelschlaeger, Tobias A.
    Hiemann, Rico
    Paetzold, Susanne
    Wieler, Lothar H.
    PLOS ONE, 2011, 6 (02):
  • [24] Probiotic therapy of prolonged non-specific diarrhoea in infants and toddlers by treatment with E. coli Nissle 1917
    Henker, J.
    Blokhin, B. M.
    Bolbot, Y. K.
    Maydannik, V. G.
    Wolff, C.
    Schulze, J.
    Sonnenborn, U.
    INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2007, 297 : 55 - 55
  • [25] Construction of recombinant E. coli Nissle 1917 (EcN) strains for the expression and secretion of defensins
    Seo, Ean-jeong
    Weibel, Stephanie
    Wehkamp, Jan
    Oelschlaeger, Tobias A.
    INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2012, 302 (06) : 276 - 287
  • [26] Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
    Tumas, Sarunas
    Meldgaard, Trine Sundebo
    Vaaben, Troels Holger
    Hernandez, Sara Suarez
    Rasmussen, Annemette Tengstedt
    Vazquez-Uribe, Ruben
    Hadrup, Sine Reker
    Sommer, Morten O. A.
    SCIENTIFIC REPORTS, 2023, 13 (01)
  • [27] Plasmid Vectors for in Vivo Selection-Free Use with the Probiotic E. coli Nissle 1917
    Kan, Anton
    Gelfat, Ilia
    Emani, Sivaram
    Praveschotinunt, Pichet
    Joshi, Neel S.
    ACS SYNTHETIC BIOLOGY, 2021, 10 (01): : 94 - 106
  • [28] Efficient markerless integration of genes in the chromosome of probiotic E. coli Nissle 1917 by bacterial conjugation
    Seco, Elena M.
    Angel Fernandez, Luis
    MICROBIAL BIOTECHNOLOGY, 2022, 15 (05): : 1374 - 1391
  • [29] E. coli Nissle 1917 modulates host glucose metabolism without directly acting on glucose
    Chavkin, Theodore A.
    Pham, Loc-Duyen
    Kostic, Aleksandar
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [30] E. coli Nissle 1917 inhibits EPEC infection by its adherence via FIC fimbria
    Kleta, S.
    Nordhoff, M.
    Tedin, K.
    Wieler, L. H.
    Oswald, S.
    Oelschlaeger, T.
    Bleiss, W.
    Holland, G.
    Schierack, P.
    INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2007, 297 : 54 - 54