Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies

Cancer immunotherapy by immune checkpoint blockade has proven its great potential by saving the lives of a proportion of late stage patients with immunogenic tumor types. However, even in these sensitive tumor types, the majority of patients do not sufficiently respond to the therapy. Furthermore, o...

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Main Authors: Ana Rita Pombo Antunes, Isabelle Scheyltjens, Johnny Duerinck, Bart Neyns, Kiavash Movahedi, Jo A Van Ginderachter
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-02-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/52176
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spelling doaj-bdbc95f3f2d646099ade0c71834ee5332021-05-05T20:47:39ZengeLife Sciences Publications LtdeLife2050-084X2020-02-01910.7554/eLife.52176Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategiesAna Rita Pombo Antunes0Isabelle Scheyltjens1Johnny Duerinck2Bart Neyns3Kiavash Movahedi4Jo A Van Ginderachter5https://orcid.org/0000-0002-4442-7474Myeloid Cell Immunology Lab, VIB Center for Inflammation Research, Brussels, Belgium; Lab of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, BelgiumMyeloid Cell Immunology Lab, VIB Center for Inflammation Research, Brussels, Belgium; Lab of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, BelgiumDepartment of Neurosurgery, UZ Brussels, Brussels, BelgiumDepartment of Medical Oncology, UZ Brussels, Brussels, BelgiumMyeloid Cell Immunology Lab, VIB Center for Inflammation Research, Brussels, Belgium; Lab of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, BelgiumMyeloid Cell Immunology Lab, VIB Center for Inflammation Research, Brussels, Belgium; Lab of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, BelgiumCancer immunotherapy by immune checkpoint blockade has proven its great potential by saving the lives of a proportion of late stage patients with immunogenic tumor types. However, even in these sensitive tumor types, the majority of patients do not sufficiently respond to the therapy. Furthermore, other tumor types, including glioblastoma, remain largely refractory. The glioblastoma immune microenvironment is recognized as highly immunosuppressive, posing a major hurdle for inducing immune-mediated destruction of cancer cells. Scattered information is available about the presence and activity of immunosuppressive or immunostimulatory cell types in glioblastoma tumors, including tumor-associated macrophages, tumor-infiltrating dendritic cells and regulatory T cells. These cell types are heterogeneous at the level of ontogeny, spatial distribution and functionality within the tumor immune compartment, providing insight in the complex cellular and molecular interplay that determines the immune refractory state in glioblastoma. This knowledge may also yield next generation molecular targets for therapeutic intervention.https://elifesciences.org/articles/52176glioblastomamicroenvironmentimmunotherapytumor-associated macrophagetumor-associated dendritic cellregulatory T cell
collection DOAJ
language English
format Article
sources DOAJ
author Ana Rita Pombo Antunes
Isabelle Scheyltjens
Johnny Duerinck
Bart Neyns
Kiavash Movahedi
Jo A Van Ginderachter
spellingShingle Ana Rita Pombo Antunes
Isabelle Scheyltjens
Johnny Duerinck
Bart Neyns
Kiavash Movahedi
Jo A Van Ginderachter
Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
eLife
glioblastoma
microenvironment
immunotherapy
tumor-associated macrophage
tumor-associated dendritic cell
regulatory T cell
author_facet Ana Rita Pombo Antunes
Isabelle Scheyltjens
Johnny Duerinck
Bart Neyns
Kiavash Movahedi
Jo A Van Ginderachter
author_sort Ana Rita Pombo Antunes
title Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
title_short Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
title_full Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
title_fullStr Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
title_full_unstemmed Understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
title_sort understanding the glioblastoma immune microenvironment as basis for the development of new immunotherapeutic strategies
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-02-01
description Cancer immunotherapy by immune checkpoint blockade has proven its great potential by saving the lives of a proportion of late stage patients with immunogenic tumor types. However, even in these sensitive tumor types, the majority of patients do not sufficiently respond to the therapy. Furthermore, other tumor types, including glioblastoma, remain largely refractory. The glioblastoma immune microenvironment is recognized as highly immunosuppressive, posing a major hurdle for inducing immune-mediated destruction of cancer cells. Scattered information is available about the presence and activity of immunosuppressive or immunostimulatory cell types in glioblastoma tumors, including tumor-associated macrophages, tumor-infiltrating dendritic cells and regulatory T cells. These cell types are heterogeneous at the level of ontogeny, spatial distribution and functionality within the tumor immune compartment, providing insight in the complex cellular and molecular interplay that determines the immune refractory state in glioblastoma. This knowledge may also yield next generation molecular targets for therapeutic intervention.
topic glioblastoma
microenvironment
immunotherapy
tumor-associated macrophage
tumor-associated dendritic cell
regulatory T cell
url https://elifesciences.org/articles/52176
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