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

被引:44
作者
Schietinger, Andrea [1 ]
Arina, Ainhoa [1 ]
Liu, Rebecca B. [1 ]
Wells, Sam [2 ]
Huang, Jianhua [3 ,4 ]
Engels, Boris [1 ]
Bindokas, Vytas [5 ]
Bartkowiak, Todd [6 ]
Lee, David [7 ]
Herrmann, Andreas [8 ,9 ]
Piston, David W. [2 ]
Pittet, Mikael J. [10 ,11 ]
Lin, P. Charles [3 ,4 ,12 ]
Zal, Tomasz [6 ]
Schreiber, Hans [1 ]
机构
[1] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[2] Vanderbilt Univ, Sch Med, Dept Physiol & Biophys, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Radiat Oncol, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Nashville, TN 37212 USA
[5] Univ Chicago, Chicago, IL USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[7] Univ Chicago, Sch Med, Chicago, IL 60637 USA
[8] Dept Canc Immunotherapeut, Duarte, CA USA
[9] Dept Tumor Immunol, Duarte, CA USA
[10] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[11] Harvard Univ, Sch Med, Boston, MA USA
[12] NCI, Ctr Canc Res, NIH, Frederick, MD 21701 USA
关键词
imaging; cancer; tumor microenvironment; tumor immunology; CD8 T cell; stroma; ANTIGENIC CANCER-CELLS; SUPPRESSOR-CELLS; STROMAL FIBROBLASTS; ESTABLISHED TUMORS; IMMUNE SUPPRESSION; CROSS-PRESENTATION; INTERFERON-GAMMA; LOSS VARIANTS; EXPRESSION; ERADICATION;
D O I
10.4161/onci.26677
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 IFN gamma 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.
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页数:14
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