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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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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. |
format | Online Article Text |
id | pubmed-3299309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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