Cardiovascular toxicity and titin cross-reactivity of affinity-enhanced T cells in myeloma and melanoma

  • Gerald P. Linette
    Siteman Cancer Center and Departments of Medicine and Pathology and Immunology, Washington University School of Medicine, St. Louis, MO;
  • Edward A. Stadtmauer
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Marcela V. Maus
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Aaron P. Rapoport
    The Greenebaum Cancer Center, University of Maryland, Baltimore, MD;
  • Bruce L. Levine
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Lyndsey Emery
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Leslie Litzky
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Adam Bagg
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Beatriz M. Carreno
    Siteman Cancer Center and Departments of Medicine and Pathology and Immunology, Washington University School of Medicine, St. Louis, MO;
  • Patrick J. Cimino
    Siteman Cancer Center and Departments of Medicine and Pathology and Immunology, Washington University School of Medicine, St. Louis, MO;
  • Gwendolyn K. Binder-Scholl
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Dominic P. Smethurst
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Andrew B. Gerry
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Nick J. Pumphrey
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Alan D. Bennett
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Joanna E. Brewer
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Joseph Dukes
    Immunocore Ltd, Abingdon, United Kingdom
  • Jane Harper
    Immunocore Ltd, Abingdon, United Kingdom
  • Helen K. Tayton-Martin
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Bent K. Jakobsen
    Adaptimmune Ltd, Philadelphia and Abingdon, United Kingdom; and
  • Namir J. Hassan
    Immunocore Ltd, Abingdon, United Kingdom
  • Michael Kalos
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;
  • Carl H. June
    Abramson Cancer Center, Department of Medicine, and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA;

書誌事項

公開日
2013-08-08
DOI
  • 10.1182/blood-2013-03-490565
公開者
American Society of Hematology

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説明

<jats:title>Key Points</jats:title> <jats:p>Engineered T-cell receptors can have redundant recognition of alternative protein motifs, resulting in severe cardiac toxicity. The use of induced pleuripotent stem cells (iPSCs) is a promising approach to identify potential off-target effects of engineered T cells.</jats:p>

収録刊行物

  • Blood

    Blood 122 (6), 863-871, 2013-08-08

    American Society of Hematology

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