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Microglia-Centered Combinatorial Strategies Against Glioblastoma
Tumor-associated microglia (MG) and macrophages (MΦ) are important components of the glioblastoma (GBM) immune tumor microenvironment (iTME). From the recent advances in understanding how MG and GBM cells evolve and interact during tumorigenesis, we emphasize the cooperation of MG with other immune...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552736/ https://www.ncbi.nlm.nih.gov/pubmed/33117364 http://dx.doi.org/10.3389/fimmu.2020.571951 |
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author | Martins, Tomás A. Schmassmann, Philip Shekarian, Tala Boulay, Jean-Louis Ritz, Marie-Françoise Zanganeh, Steven vom Berg, Johannes Hutter, Gregor |
author_facet | Martins, Tomás A. Schmassmann, Philip Shekarian, Tala Boulay, Jean-Louis Ritz, Marie-Françoise Zanganeh, Steven vom Berg, Johannes Hutter, Gregor |
author_sort | Martins, Tomás A. |
collection | PubMed |
description | Tumor-associated microglia (MG) and macrophages (MΦ) are important components of the glioblastoma (GBM) immune tumor microenvironment (iTME). From the recent advances in understanding how MG and GBM cells evolve and interact during tumorigenesis, we emphasize the cooperation of MG with other immune cell types of the GBM-iTME, mainly MΦ and T cells. We provide a comprehensive overview of current immunotherapeutic clinical trials and approaches for the treatment of GBM, which in general, underestimate the counteracting contribution of immunosuppressive MG as a main factor for treatment failure. Furthermore, we summarize new developments and strategies in MG reprogramming/re-education in the GBM context, with a focus on ways to boost MG-mediated tumor cell phagocytosis and associated experimental models and methods. This ultimately converges in our proposal of novel combinatorial regimens that locally modulate MG as a central paradigm, and therefore may lead to additional, long-lasting, and effective tumoricidal responses. |
format | Online Article Text |
id | pubmed-7552736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75527362020-10-27 Microglia-Centered Combinatorial Strategies Against Glioblastoma Martins, Tomás A. Schmassmann, Philip Shekarian, Tala Boulay, Jean-Louis Ritz, Marie-Françoise Zanganeh, Steven vom Berg, Johannes Hutter, Gregor Front Immunol Immunology Tumor-associated microglia (MG) and macrophages (MΦ) are important components of the glioblastoma (GBM) immune tumor microenvironment (iTME). From the recent advances in understanding how MG and GBM cells evolve and interact during tumorigenesis, we emphasize the cooperation of MG with other immune cell types of the GBM-iTME, mainly MΦ and T cells. We provide a comprehensive overview of current immunotherapeutic clinical trials and approaches for the treatment of GBM, which in general, underestimate the counteracting contribution of immunosuppressive MG as a main factor for treatment failure. Furthermore, we summarize new developments and strategies in MG reprogramming/re-education in the GBM context, with a focus on ways to boost MG-mediated tumor cell phagocytosis and associated experimental models and methods. This ultimately converges in our proposal of novel combinatorial regimens that locally modulate MG as a central paradigm, and therefore may lead to additional, long-lasting, and effective tumoricidal responses. Frontiers Media S.A. 2020-09-29 /pmc/articles/PMC7552736/ /pubmed/33117364 http://dx.doi.org/10.3389/fimmu.2020.571951 Text en Copyright © 2020 Martins, Schmassmann, Shekarian, Boulay, Ritz, Zanganeh, vom Berg and Hutter. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Martins, Tomás A. Schmassmann, Philip Shekarian, Tala Boulay, Jean-Louis Ritz, Marie-Françoise Zanganeh, Steven vom Berg, Johannes Hutter, Gregor Microglia-Centered Combinatorial Strategies Against Glioblastoma |
title | Microglia-Centered Combinatorial Strategies Against Glioblastoma |
title_full | Microglia-Centered Combinatorial Strategies Against Glioblastoma |
title_fullStr | Microglia-Centered Combinatorial Strategies Against Glioblastoma |
title_full_unstemmed | Microglia-Centered Combinatorial Strategies Against Glioblastoma |
title_short | Microglia-Centered Combinatorial Strategies Against Glioblastoma |
title_sort | microglia-centered combinatorial strategies against glioblastoma |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552736/ https://www.ncbi.nlm.nih.gov/pubmed/33117364 http://dx.doi.org/10.3389/fimmu.2020.571951 |
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