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

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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895414/
https://www.ncbi.nlm.nih.gov/pubmed/24482750
http://dx.doi.org/10.4161/onci.26677
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author 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
author_facet 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
author_sort Schietinger, Andrea
collection PubMed
description 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.
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spelling pubmed-38954142014-01-30 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 Oncoimmunology Original Research 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. Landes Bioscience 2013-11-01 2013-11-04 /pmc/articles/PMC3895414/ /pubmed/24482750 http://dx.doi.org/10.4161/onci.26677 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Original Research
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
Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer
title Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer
title_full Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer
title_fullStr Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer
title_full_unstemmed Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer
title_short Longitudinal confocal microscopy imaging of solid tumor destruction following adoptive T cell transfer
title_sort longitudinal confocal microscopy imaging of solid tumor destruction following adoptive t cell transfer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895414/
https://www.ncbi.nlm.nih.gov/pubmed/24482750
http://dx.doi.org/10.4161/onci.26677
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