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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Main Authors: Elodie Vauleon, Tony Avril, Brigitte Collet, Jean Mosser, Véronique Quillien
Format: Article
Language:English
Published: Hindawi Limited 2010-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2010/689171
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spelling 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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