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The therapeutic landscape for cells engineered with chimeric antigen receptors.
MacKay, Matthew; Afshinnekoo, Ebrahim; Rub, Jonathan; Hassan, Ciaran; Khunte, Mihir; Baskaran, Nithyashri; Owens, Bryan; Liu, Lauren; Roboz, Gail J; Guzman, Monica L; Melnick, Ari M; Wu, Shixiu; Mason, Christopher E.
Afiliación
  • MacKay M; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
  • Afshinnekoo E; The WorldQuant Initiative for Quantitative Prediction, Weill Cornell Medicine, New York, NY, USA.
  • Rub J; The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.
  • Hassan C; Tri-Institutional Computational Biology and Medicine Program, Weill Cornell Medicine of Cornell University, New York, NY, USA.
  • Khunte M; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
  • Baskaran N; The WorldQuant Initiative for Quantitative Prediction, Weill Cornell Medicine, New York, NY, USA.
  • Owens B; The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.
  • Liu L; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
  • Roboz GJ; The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.
  • Guzman ML; Yale University, New Haven, CT, USA.
  • Melnick AM; Yale University, New Haven, CT, USA.
  • Wu S; Yale University, New Haven, CT, USA.
  • Mason CE; Yale University, New Haven, CT, USA.
Nat Biotechnol ; 38(2): 233-244, 2020 02.
Article en En | MEDLINE | ID: mdl-31907405
Despite the global rapid increase in the number of clinical trials employing chimeric antigen receptors (CARs), no comprehensive survey of their scope, targets and design exists. In this study, we present an interactive CAR clinical trial database, spanning 64 targets deployed in T cells (CAR-T), natural killer cells (CAR-NK) or mixtures (CAR-NK/T) from over 500 clinical trials in 20 countries, encompassing >20,000 patients. By combining these data with transcriptional and proteomic data, we create a 'targetable landscape' for CAR cell therapies based on 13,206 proteins and RNAs across 78 tissues, 124 cell types and 20 cancer types. These data suggest a landscape of over 100 single targets and over 100,000 target pairs using logical switches for CAR cell engineering. Our analysis of the CAR cellular therapeutic landscape may aid the design of future therapies, improve target-to-patient matching, and ultimately help inform our understanding of CAR therapy's safety and efficacy.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ingeniería Celular / Receptores Quiméricos de Antígenos Límite: Humans Idioma: En Revista: Nat Biotechnol Asunto de la revista: BIOTECNOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ingeniería Celular / Receptores Quiméricos de Antígenos Límite: Humans Idioma: En Revista: Nat Biotechnol Asunto de la revista: BIOTECNOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos