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Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme

Treatment of patients with glioblastoma multiforme (GBM) remains to be a challenge with a median survival of 14.6 months following diagnosis. Standard treatment options include surgery, radiation therapy, and systemic chemotherapy with temozolomide. Despite the fact that the brain constitutes an imm...

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Detalles Bibliográficos
Autores principales: Xu, Xun, Stockhammer, Florian, Schmitt, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299309/
https://www.ncbi.nlm.nih.gov/pubmed/22474481
http://dx.doi.org/10.1155/2012/764213
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author Xu, Xun
Stockhammer, Florian
Schmitt, Michael
author_facet Xu, Xun
Stockhammer, Florian
Schmitt, Michael
author_sort Xu, Xun
collection PubMed
description Treatment of patients with glioblastoma multiforme (GBM) remains to be a challenge with a median survival of 14.6 months following diagnosis. Standard treatment options include surgery, radiation therapy, and systemic chemotherapy with temozolomide. Despite the fact that the brain constitutes an immunoprivileged site, recent observations after immunotherapies with lysate from autologous tumor cells pulsed on dendritic cells (DCs), peptides, protein, messenger RNA, and cytokines suggest an immunological and even clinical response from immunotherapies. Given this plethora of immunomodulatory therapies, this paper gives a structure overview of the state-of-the art in the field. Particular emphasis was also put on immunogenic antigens as potential targets for a more specific stimulation of the immune system against GBM.
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spelling pubmed-32993092012-04-03 Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme Xu, Xun Stockhammer, Florian Schmitt, Michael Clin Dev Immunol Review Article Treatment of patients with glioblastoma multiforme (GBM) remains to be a challenge with a median survival of 14.6 months following diagnosis. Standard treatment options include surgery, radiation therapy, and systemic chemotherapy with temozolomide. Despite the fact that the brain constitutes an immunoprivileged site, recent observations after immunotherapies with lysate from autologous tumor cells pulsed on dendritic cells (DCs), peptides, protein, messenger RNA, and cytokines suggest an immunological and even clinical response from immunotherapies. Given this plethora of immunomodulatory therapies, this paper gives a structure overview of the state-of-the art in the field. Particular emphasis was also put on immunogenic antigens as potential targets for a more specific stimulation of the immune system against GBM. Hindawi Publishing Corporation 2012 2012-02-28 /pmc/articles/PMC3299309/ /pubmed/22474481 http://dx.doi.org/10.1155/2012/764213 Text en Copyright © 2012 Xun Xu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Xu, Xun
Stockhammer, Florian
Schmitt, Michael
Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme
title Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme
title_full Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme
title_fullStr Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme
title_full_unstemmed Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme
title_short Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme
title_sort cellular-based immunotherapies for patients with glioblastoma multiforme
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299309/
https://www.ncbi.nlm.nih.gov/pubmed/22474481
http://dx.doi.org/10.1155/2012/764213
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