Overview of Cellular Immunotherapy for Patients with Glioblastoma
High grade gliomas (HGG) including glioblastomas (GBM) are the most common and devastating primary brain tumours. Despite important progresses in GBM treatment that currently includes surgery combined to radio- and chemotherapy, GBM patients' prognosis remains very poor. Immunotherapy is one of...
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Online Access: | http://dx.doi.org/10.1155/2010/689171 |
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doaj-0e255c1042be45988da8c0e70f47df2d2020-11-25T00:22:47ZengHindawi LimitedClinical and Developmental Immunology1740-25221740-25302010-01-01201010.1155/2010/689171689171Overview of Cellular Immunotherapy for Patients with GlioblastomaElodie Vauleon0Tony Avril1Brigitte Collet2Jean Mosser3Véronique Quillien4Département de Biologie, Centre Eugène Marquis, Rue de la bataille Flandres Dunkerque, CS44229, 35042 Rennes cedex, FranceDépartement de Biologie, Centre Eugène Marquis, Rue de la bataille Flandres Dunkerque, CS44229, 35042 Rennes cedex, FranceDépartement de Biologie, Centre Eugène Marquis, Rue de la bataille Flandres Dunkerque, CS44229, 35042 Rennes cedex, FranceUMR6061 CNRS, Université de Rennes 1, IFR 140, CS34317, 35043 Rennes cedex, FranceDépartement de Biologie, Centre Eugène Marquis, Rue de la bataille Flandres Dunkerque, CS44229, 35042 Rennes cedex, FranceHigh grade gliomas (HGG) including glioblastomas (GBM) are the most common and devastating primary brain tumours. Despite important progresses in GBM treatment that currently includes surgery combined to radio- and chemotherapy, GBM patients' prognosis remains very poor. Immunotherapy is one of the new promising therapeutic approaches that can specifically target tumour cells. Such an approach could also maintain long term antitumour responses without inducing neurologic defects. Since the past 25 years, adoptive and active immunotherapies using lymphokine-activated killer cells, cytotoxic T cells, tumour-infiltrating lymphocytes, autologous tumour cells, and dendritic cells have been tested in phase I/II clinical trials with HGG patients. This paper inventories these cellular immunotherapeutic strategies and discusses their efficacy, limits, and future perspectives for optimizing the treatment to achieve clinical benefits for GBM patients.http://dx.doi.org/10.1155/2010/689171 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elodie Vauleon Tony Avril Brigitte Collet Jean Mosser Véronique Quillien |
spellingShingle |
Elodie Vauleon Tony Avril Brigitte Collet Jean Mosser Véronique Quillien Overview of Cellular Immunotherapy for Patients with Glioblastoma Clinical and Developmental Immunology |
author_facet |
Elodie Vauleon Tony Avril Brigitte Collet Jean Mosser Véronique Quillien |
author_sort |
Elodie Vauleon |
title |
Overview of Cellular Immunotherapy for Patients with Glioblastoma |
title_short |
Overview of Cellular Immunotherapy for Patients with Glioblastoma |
title_full |
Overview of Cellular Immunotherapy for Patients with Glioblastoma |
title_fullStr |
Overview of Cellular Immunotherapy for Patients with Glioblastoma |
title_full_unstemmed |
Overview of Cellular Immunotherapy for Patients with Glioblastoma |
title_sort |
overview of cellular immunotherapy for patients with glioblastoma |
publisher |
Hindawi Limited |
series |
Clinical and Developmental Immunology |
issn |
1740-2522 1740-2530 |
publishDate |
2010-01-01 |
description |
High grade gliomas (HGG) including glioblastomas (GBM) are the most common and devastating primary brain tumours. Despite important progresses in GBM treatment that currently includes surgery combined to radio- and chemotherapy, GBM patients' prognosis remains very poor. Immunotherapy is one of the new promising therapeutic approaches that can specifically target tumour cells. Such an approach could also maintain long term antitumour responses without inducing neurologic defects. Since the past 25 years, adoptive and active immunotherapies using lymphokine-activated killer cells, cytotoxic T cells, tumour-infiltrating lymphocytes, autologous tumour cells, and dendritic cells have been tested in phase I/II clinical trials with HGG patients. This paper inventories these cellular immunotherapeutic strategies and discusses their efficacy, limits, and future perspectives for optimizing the treatment to achieve clinical benefits for GBM patients. |
url |
http://dx.doi.org/10.1155/2010/689171 |
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