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Oncoimmunology. 2013 Nov 1;2(11):e26677. Epub 2013 Nov 4.

Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer.

Author information

  • 1Department of Pathology; The University of Chicago; Chicago, IL USA.
  • 2Department of Physiology and Biophysics; Vanderbilt University School of Medicine; Nashville, TN USA.
  • 3Department of Radiation Oncology and The Vanderbilt-Ingram Cancer Center; Vanderbilt University School of Medicine; Nashville, TN USA.
  • 4Integrated Microscopy Core; The University of Chicago; Chicago, IL USA.
  • 5Department of Immunology; The University of Texas MD Anderson Cancer Center; Houston, TX USA.
  • 6School of Medicine; The University of Chicago; Chicago, IL USA.
  • 7Departments of Cancer Immunotherapeutics & Tumor Immunology; City of Hope; Duarte, CA USA.
  • 8Center for Systems Biology; Massachusetts General Hospital and Harvard Medical School; Boston, MA USA.
  • 9Department 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.

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.

KEYWORDS:

CD8 T cell; cancer; imaging; stroma; tumor immunology; tumor microenvironment

PMID:
24482750
[PubMed]
PMCID:
PMC3895414
Free PMC Article

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