author_facet Lohr, Jennifer
Ratliff, Thomas
Huppertz, Andrea
Ge, Yingzi
Dictus, Christine
Ahmadi, Rezvan
Grau, Stefan
Hiraoka, Nobuyoshi
Eckstein, Volker
Ecker, Rupert C.
Korff, Thomas
von Deimling, Andreas
Unterberg, Andreas
Beckhove, Philipp
Herold-Mende, Christel
Lohr, Jennifer
Ratliff, Thomas
Huppertz, Andrea
Ge, Yingzi
Dictus, Christine
Ahmadi, Rezvan
Grau, Stefan
Hiraoka, Nobuyoshi
Eckstein, Volker
Ecker, Rupert C.
Korff, Thomas
von Deimling, Andreas
Unterberg, Andreas
Beckhove, Philipp
Herold-Mende, Christel
author Lohr, Jennifer
Ratliff, Thomas
Huppertz, Andrea
Ge, Yingzi
Dictus, Christine
Ahmadi, Rezvan
Grau, Stefan
Hiraoka, Nobuyoshi
Eckstein, Volker
Ecker, Rupert C.
Korff, Thomas
von Deimling, Andreas
Unterberg, Andreas
Beckhove, Philipp
Herold-Mende, Christel
spellingShingle Lohr, Jennifer
Ratliff, Thomas
Huppertz, Andrea
Ge, Yingzi
Dictus, Christine
Ahmadi, Rezvan
Grau, Stefan
Hiraoka, Nobuyoshi
Eckstein, Volker
Ecker, Rupert C.
Korff, Thomas
von Deimling, Andreas
Unterberg, Andreas
Beckhove, Philipp
Herold-Mende, Christel
Clinical Cancer Research
Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
Cancer Research
Oncology
author_sort lohr, jennifer
spelling Lohr, Jennifer Ratliff, Thomas Huppertz, Andrea Ge, Yingzi Dictus, Christine Ahmadi, Rezvan Grau, Stefan Hiraoka, Nobuyoshi Eckstein, Volker Ecker, Rupert C. Korff, Thomas von Deimling, Andreas Unterberg, Andreas Beckhove, Philipp Herold-Mende, Christel 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-10-2557 <jats:title>Abstract</jats:title> <jats:p>Purpose: In glioma—in contrast to various other cancers—the impact of T-lymphocytes on clinical outcome is not clear. We investigated the clinical relevance and regulation of T-cell infiltration in glioma.</jats:p> <jats:p>Experimental Design: T-cell subpopulations from entire sections of 93 WHO°II–IV gliomas were computationally identified using markers CD3, CD8, and Foxp3; survival analysis was then done on primary glioblastomas (pGBM). Endothelial cells expressing cellular adhesion molecules (CAM) were similarly computationally quantified from the same glioma tissues. Influence of prominent cytokines (as measured by ELISA from 53 WHO°II–IV glioma lysates) on CAM-expression in GBM-isolated endothelial cells was determined using flow cytometry. The functional relevance of the cytokine-mediated CAM regulation was tested in a transmigration assay using GBM-derived endothelial cells and autologous T-cells.</jats:p> <jats:p>Results: Infiltration of all T-cell subsets increased in high-grade tumors. Most strikingly, within pGBM, elevated numbers of intratumoral effector T cells (Teff, cytotoxic and helper) significantly correlated with a better survival; regulatory T cells were infrequently present and not associated with GBM patient outcome. Interestingly, increased infiltration of Teff cells was related to the expression of ICAM-1 on the vessel surface. Transmigration of autologous T cells in vitro was markedly reduced in the presence of CAM-blocking antibodies. We found that TGF-β molecules impeded transmigration and downregulated CAM-expression on GBM-isolated endothelial cells; blocking TGF-β receptor signaling increased transmigration.</jats:p> <jats:p>Conclusions: This study provides comprehensive and novel insights into occurrence and regulation of T-cell infiltration in glioma. Specifically, targeting TGF-β1 and TGF-β2 might improve intratumoral T-cell infiltration and thus enhance effectiveness of immunotherapeutic approaches. Clin Cancer Res; 17(13); 4296–308. ©2011 AACR.</jats:p> Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β Clinical Cancer Research
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recordtype ai
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series Clinical Cancer Research
source_id 49
title Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_unstemmed Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_full Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_fullStr Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_full_unstemmed Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_short Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_sort effector t-cell infiltration positively impacts survival of glioblastoma patients and is impaired by tumor-derived tgf-β
topic Cancer Research
Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-10-2557
publishDate 2011
physical 4296-4308
description <jats:title>Abstract</jats:title> <jats:p>Purpose: In glioma—in contrast to various other cancers—the impact of T-lymphocytes on clinical outcome is not clear. We investigated the clinical relevance and regulation of T-cell infiltration in glioma.</jats:p> <jats:p>Experimental Design: T-cell subpopulations from entire sections of 93 WHO°II–IV gliomas were computationally identified using markers CD3, CD8, and Foxp3; survival analysis was then done on primary glioblastomas (pGBM). Endothelial cells expressing cellular adhesion molecules (CAM) were similarly computationally quantified from the same glioma tissues. Influence of prominent cytokines (as measured by ELISA from 53 WHO°II–IV glioma lysates) on CAM-expression in GBM-isolated endothelial cells was determined using flow cytometry. The functional relevance of the cytokine-mediated CAM regulation was tested in a transmigration assay using GBM-derived endothelial cells and autologous T-cells.</jats:p> <jats:p>Results: Infiltration of all T-cell subsets increased in high-grade tumors. Most strikingly, within pGBM, elevated numbers of intratumoral effector T cells (Teff, cytotoxic and helper) significantly correlated with a better survival; regulatory T cells were infrequently present and not associated with GBM patient outcome. Interestingly, increased infiltration of Teff cells was related to the expression of ICAM-1 on the vessel surface. Transmigration of autologous T cells in vitro was markedly reduced in the presence of CAM-blocking antibodies. We found that TGF-β molecules impeded transmigration and downregulated CAM-expression on GBM-isolated endothelial cells; blocking TGF-β receptor signaling increased transmigration.</jats:p> <jats:p>Conclusions: This study provides comprehensive and novel insights into occurrence and regulation of T-cell infiltration in glioma. Specifically, targeting TGF-β1 and TGF-β2 might improve intratumoral T-cell infiltration and thus enhance effectiveness of immunotherapeutic approaches. Clin Cancer Res; 17(13); 4296–308. ©2011 AACR.</jats:p>
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author Lohr, Jennifer, Ratliff, Thomas, Huppertz, Andrea, Ge, Yingzi, Dictus, Christine, Ahmadi, Rezvan, Grau, Stefan, Hiraoka, Nobuyoshi, Eckstein, Volker, Ecker, Rupert C., Korff, Thomas, von Deimling, Andreas, Unterberg, Andreas, Beckhove, Philipp, Herold-Mende, Christel
author_facet Lohr, Jennifer, Ratliff, Thomas, Huppertz, Andrea, Ge, Yingzi, Dictus, Christine, Ahmadi, Rezvan, Grau, Stefan, Hiraoka, Nobuyoshi, Eckstein, Volker, Ecker, Rupert C., Korff, Thomas, von Deimling, Andreas, Unterberg, Andreas, Beckhove, Philipp, Herold-Mende, Christel, Lohr, Jennifer, Ratliff, Thomas, Huppertz, Andrea, Ge, Yingzi, Dictus, Christine, Ahmadi, Rezvan, Grau, Stefan, Hiraoka, Nobuyoshi, Eckstein, Volker, Ecker, Rupert C., Korff, Thomas, von Deimling, Andreas, Unterberg, Andreas, Beckhove, Philipp, Herold-Mende, Christel
author_sort lohr, jennifer
container_issue 13
container_start_page 4296
container_title Clinical Cancer Research
container_volume 17
description <jats:title>Abstract</jats:title> <jats:p>Purpose: In glioma—in contrast to various other cancers—the impact of T-lymphocytes on clinical outcome is not clear. We investigated the clinical relevance and regulation of T-cell infiltration in glioma.</jats:p> <jats:p>Experimental Design: T-cell subpopulations from entire sections of 93 WHO°II–IV gliomas were computationally identified using markers CD3, CD8, and Foxp3; survival analysis was then done on primary glioblastomas (pGBM). Endothelial cells expressing cellular adhesion molecules (CAM) were similarly computationally quantified from the same glioma tissues. Influence of prominent cytokines (as measured by ELISA from 53 WHO°II–IV glioma lysates) on CAM-expression in GBM-isolated endothelial cells was determined using flow cytometry. The functional relevance of the cytokine-mediated CAM regulation was tested in a transmigration assay using GBM-derived endothelial cells and autologous T-cells.</jats:p> <jats:p>Results: Infiltration of all T-cell subsets increased in high-grade tumors. Most strikingly, within pGBM, elevated numbers of intratumoral effector T cells (Teff, cytotoxic and helper) significantly correlated with a better survival; regulatory T cells were infrequently present and not associated with GBM patient outcome. Interestingly, increased infiltration of Teff cells was related to the expression of ICAM-1 on the vessel surface. Transmigration of autologous T cells in vitro was markedly reduced in the presence of CAM-blocking antibodies. We found that TGF-β molecules impeded transmigration and downregulated CAM-expression on GBM-isolated endothelial cells; blocking TGF-β receptor signaling increased transmigration.</jats:p> <jats:p>Conclusions: This study provides comprehensive and novel insights into occurrence and regulation of T-cell infiltration in glioma. Specifically, targeting TGF-β1 and TGF-β2 might improve intratumoral T-cell infiltration and thus enhance effectiveness of immunotherapeutic approaches. Clin Cancer Res; 17(13); 4296–308. ©2011 AACR.</jats:p>
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imprint_str_mv American Association for Cancer Research (AACR), 2011
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spelling Lohr, Jennifer Ratliff, Thomas Huppertz, Andrea Ge, Yingzi Dictus, Christine Ahmadi, Rezvan Grau, Stefan Hiraoka, Nobuyoshi Eckstein, Volker Ecker, Rupert C. Korff, Thomas von Deimling, Andreas Unterberg, Andreas Beckhove, Philipp Herold-Mende, Christel 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-10-2557 <jats:title>Abstract</jats:title> <jats:p>Purpose: In glioma—in contrast to various other cancers—the impact of T-lymphocytes on clinical outcome is not clear. We investigated the clinical relevance and regulation of T-cell infiltration in glioma.</jats:p> <jats:p>Experimental Design: T-cell subpopulations from entire sections of 93 WHO°II–IV gliomas were computationally identified using markers CD3, CD8, and Foxp3; survival analysis was then done on primary glioblastomas (pGBM). Endothelial cells expressing cellular adhesion molecules (CAM) were similarly computationally quantified from the same glioma tissues. Influence of prominent cytokines (as measured by ELISA from 53 WHO°II–IV glioma lysates) on CAM-expression in GBM-isolated endothelial cells was determined using flow cytometry. The functional relevance of the cytokine-mediated CAM regulation was tested in a transmigration assay using GBM-derived endothelial cells and autologous T-cells.</jats:p> <jats:p>Results: Infiltration of all T-cell subsets increased in high-grade tumors. Most strikingly, within pGBM, elevated numbers of intratumoral effector T cells (Teff, cytotoxic and helper) significantly correlated with a better survival; regulatory T cells were infrequently present and not associated with GBM patient outcome. Interestingly, increased infiltration of Teff cells was related to the expression of ICAM-1 on the vessel surface. Transmigration of autologous T cells in vitro was markedly reduced in the presence of CAM-blocking antibodies. We found that TGF-β molecules impeded transmigration and downregulated CAM-expression on GBM-isolated endothelial cells; blocking TGF-β receptor signaling increased transmigration.</jats:p> <jats:p>Conclusions: This study provides comprehensive and novel insights into occurrence and regulation of T-cell infiltration in glioma. Specifically, targeting TGF-β1 and TGF-β2 might improve intratumoral T-cell infiltration and thus enhance effectiveness of immunotherapeutic approaches. Clin Cancer Res; 17(13); 4296–308. ©2011 AACR.</jats:p> Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β Clinical Cancer Research
spellingShingle Lohr, Jennifer, Ratliff, Thomas, Huppertz, Andrea, Ge, Yingzi, Dictus, Christine, Ahmadi, Rezvan, Grau, Stefan, Hiraoka, Nobuyoshi, Eckstein, Volker, Ecker, Rupert C., Korff, Thomas, von Deimling, Andreas, Unterberg, Andreas, Beckhove, Philipp, Herold-Mende, Christel, Clinical Cancer Research, Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β, Cancer Research, Oncology
title Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_full Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_fullStr Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_full_unstemmed Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_short Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
title_sort effector t-cell infiltration positively impacts survival of glioblastoma patients and is impaired by tumor-derived tgf-β
title_unstemmed Effector T-Cell Infiltration Positively Impacts Survival of Glioblastoma Patients and Is Impaired by Tumor-Derived TGF-β
topic Cancer Research, Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-10-2557