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A rapid in vitro methodology for simultaneous target discovery and antibody generation against functional cell subpopulations.
Nixon, Allison M L; Duque, Alejandro; Yelle, Nicholas; McLaughlin, Megan; Davoudi, Sadegh; Pedley, Nicolas M; Haynes, Jennifer; Brown, Kevin R; Pan, James; Hart, Traver; Gilbert, Penney M; Singh, Sheila K; O'Brien, Catherine A; Sidhu, Sachdev S; Moffat, Jason.
Afiliación
  • Nixon AML; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • Duque A; Department of Molecular Genetics, University of Toronto, Toronto, M5S 1A8, Canada.
  • Yelle N; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • McLaughlin M; Stem Cell and Cancer Research Institute, McMaster University, Hamilton, L8S 4K1, Canada.
  • Davoudi S; Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, L8N 3Z5, Canada.
  • Pedley NM; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • Haynes J; Department of Molecular Genetics, University of Toronto, Toronto, M5S 1A8, Canada.
  • Brown KR; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • Pan J; Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, M5S 3G9, Canada.
  • Hart T; Princess Margaret Cancer Centre, University Health Network, Toronto, M5G 2MC1, Canada.
  • Gilbert PM; Princess Margaret Cancer Centre, University Health Network, Toronto, M5G 2MC1, Canada.
  • Singh SK; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • O'Brien CA; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • Sidhu SS; Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
  • Moffat J; Department of Bioinformatics and Computational Biology, MD Anderson Cancer Center, Houston, Texas, 77030, USA.
Sci Rep ; 9(1): 842, 2019 01 29.
Article en En | MEDLINE | ID: mdl-30696911
Cell surface antigen discovery is of great interest for biomedical research both for isolation of rare cell populations and therapeutic targeting. We developed a rapid, cost-effective, fully in vitro technology which facilities the simultaneous target discovery and human antibody generation on the surface of virtually any cell population of interest. We apply our technique to human colorectal cancer-initiating cells (CICs) and identify hundreds of unique human antibodies. We characterized the top three antibody candidates targeting these CICs and identify their protein targets as integrin α7 (ITGA7), HLA-A1 and integrin ß6 (ITGB6). We demonstrate that these antibodies can be used to isolate self-renewing colorectal CICs, and that the integrin α7 antibody can prospectively identify glioblastoma brain tumor initiating cells as well as human muscle stem cells. We also demonstrate that genetic ablation of integrin ß6 impedes colorectal CIC function. The methodology can be readily applied to other cell populations including stem cells, cancer, or immune cells to facilitate the rapid identification of novel targets and simultaneous generation of potent and specific antibodies with therapeutic potential.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Biomarcadores de Tumor / Glioblastoma / Anticuerpos / Antígenos de Superficie Límite: Humans Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Biomarcadores de Tumor / Glioblastoma / Anticuerpos / Antígenos de Superficie Límite: Humans Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article País de afiliación: Canadá
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