Your browser doesn't support javascript.
loading
Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer.
Schietinger, Andrea; Arina, Ainhoa; Liu, Rebecca B; Wells, Sam; Huang, Jianhua; Engels, Boris; Bindokas, Vytas; Bartkowiak, Todd; Lee, David; Herrmann, Andreas; Piston, David W; Pittet, Mikael J; Lin, P Charles; Zal, Tomasz; Schreiber, Hans.
Afiliación
  • Schietinger A; Department of Pathology; The University of Chicago; Chicago, IL USA.
  • Arina A; Department of Pathology; The University of Chicago; Chicago, IL USA.
  • Liu RB; Department of Pathology; The University of Chicago; Chicago, IL USA.
  • Wells S; Department of Physiology and Biophysics; Vanderbilt University School of Medicine; Nashville, TN USA.
  • Huang J; Department of Radiation Oncology and The Vanderbilt-Ingram Cancer Center; Vanderbilt University School of Medicine; Nashville, TN USA.
  • Engels B; Department of Pathology; The University of Chicago; Chicago, IL USA.
  • Bindokas V; Integrated Microscopy Core; The University of Chicago; Chicago, IL USA.
  • Bartkowiak T; Department of Immunology; The University of Texas MD Anderson Cancer Center; Houston, TX USA.
  • Lee D; School of Medicine; The University of Chicago; Chicago, IL USA.
  • Herrmann A; Departments of Cancer Immunotherapeutics & Tumor Immunology; City of Hope; Duarte, CA USA.
  • Piston DW; Department of Physiology and Biophysics; Vanderbilt University School of Medicine; Nashville, TN USA.
  • Pittet MJ; Center for Systems Biology; Massachusetts General Hospital and Harvard Medical School; Boston, MA USA.
  • Lin PC; Department of Radiation Oncology and The Vanderbilt-Ingram Cancer Center; Vanderbilt University School of Medicine; Nashville, TN USA ; Center for Cancer Research; National Cancer Institute, NIH; Frederick, MD USA.
  • Zal T; Department of Immunology; The University of Texas MD Anderson Cancer Center; Houston, TX USA.
  • Schreiber H; Department of Pathology; The University of Chicago; Chicago, IL USA.
Oncoimmunology ; 2(11): e26677, 2013 Nov 01.
Article en En | MEDLINE | ID: mdl-24482750
ABSTRACT
A fluorescence-based, high-resolution imaging approach was used to visualize longitudinally the cellular events unfolding during T cell-mediated tumor destruction. The dynamic interplay of T cells, cancer cells, cancer antigen loss variants, and stromal cells-all color-coded in vivo-was analyzed in established, solid tumors that had developed behind windows implanted on the backs of mice. Events could be followed repeatedly within precisely the same tumor region-before, during and after adoptive T cell therapy-thereby enabling for the first time a longitudinal in vivo evaluation of protracted events, an analysis not possible with terminal imaging of surgically exposed tumors. T cell infiltration, stromal interactions, and vessel destruction, as well as the functional consequences thereof, including the elimination of cancer cells and cancer cell variants were studied. Minimal perivascular T cell infiltrates initiated vascular destruction inside the tumor mass eventually leading to macroscopic central tumor necrosis. Prolonged engagement of T cells with tumor antigen-crosspresenting stromal cells correlated with high IFNγ cytokine release and bystander elimination of antigen-negative cancer cells. The high-resolution, longitudinal, in vivo imaging approach described here will help to further a better mechanistic understanding of tumor eradication by T cells and other anti-cancer therapies.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncoimmunology Año: 2013 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncoimmunology Año: 2013 Tipo del documento: Article