The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy

Glioblastoma (GBM) is the most common and aggressive malignant primary brain tumor in adults. Its aggressive nature is attributed partly to its deeply invasive margins, its molecular and cellular heterogeneity, and uniquely tolerant site of origin—the brain. The immunosuppressive central nervous sys...

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Main Authors: Fiona A. Desland, Adília Hormigo
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/19/7358
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spelling doaj-1c2f7519de844e2cb2feb84e00c822932020-11-25T03:35:32ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-10-01217358735810.3390/ijms21197358The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma ImmunotherapyFiona A. Desland0Adília Hormigo1Icahn School of Medicine at Mount Sinai, The Tisch Cancer Institute, Department of Neurology, Box 1137, 1 Gustave L. Levy Pl, New York, NY 10029-6574, USAIcahn School of Medicine at Mount Sinai, The Tisch Cancer Institute, Department of Neurology, Box 1137, 1 Gustave L. Levy Pl, New York, NY 10029-6574, USAGlioblastoma (GBM) is the most common and aggressive malignant primary brain tumor in adults. Its aggressive nature is attributed partly to its deeply invasive margins, its molecular and cellular heterogeneity, and uniquely tolerant site of origin—the brain. The immunosuppressive central nervous system (CNS) and GBM microenvironments are significant obstacles to generating an effective and long-lasting anti-tumoral response, as evidenced by this tumor’s reduced rate of treatment response and high probability of recurrence. Immunotherapy has revolutionized patients’ outcomes across many cancers and may open new avenues for patients with GBM. There is now a range of immunotherapeutic strategies being tested in patients with GBM that target both the innate and adaptive immune compartment. These strategies include antibodies that re-educate tumor macrophages, vaccines that introduce tumor-specific dendritic cells, checkpoint molecule inhibition, engineered T cells, and proteins that help T cells engage directly with tumor cells. Despite this, there is still much ground to be gained in improving the response rates of the various immunotherapies currently being trialed. Through historical and contemporary studies, we examine the fundamentals of CNS immunity that shape how to approach immune modulation in GBM, including the now revamped concept of CNS privilege. We also discuss the preclinical models used to study GBM progression and immunity. Lastly, we discuss the immunotherapeutic strategies currently being studied to help overcome the hurdles of the blood–brain barrier and the immunosuppressive tumor microenvironment.https://www.mdpi.com/1422-0067/21/19/7358CNS immunitytumor microenvironmentglioblastomaimmunotherapy
collection DOAJ
language English
format Article
sources DOAJ
author Fiona A. Desland
Adília Hormigo
spellingShingle Fiona A. Desland
Adília Hormigo
The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
International Journal of Molecular Sciences
CNS immunity
tumor microenvironment
glioblastoma
immunotherapy
author_facet Fiona A. Desland
Adília Hormigo
author_sort Fiona A. Desland
title The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
title_short The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
title_full The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
title_fullStr The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
title_full_unstemmed The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
title_sort cns and the brain tumor microenvironment: implications for glioblastoma immunotherapy
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-10-01
description Glioblastoma (GBM) is the most common and aggressive malignant primary brain tumor in adults. Its aggressive nature is attributed partly to its deeply invasive margins, its molecular and cellular heterogeneity, and uniquely tolerant site of origin—the brain. The immunosuppressive central nervous system (CNS) and GBM microenvironments are significant obstacles to generating an effective and long-lasting anti-tumoral response, as evidenced by this tumor’s reduced rate of treatment response and high probability of recurrence. Immunotherapy has revolutionized patients’ outcomes across many cancers and may open new avenues for patients with GBM. There is now a range of immunotherapeutic strategies being tested in patients with GBM that target both the innate and adaptive immune compartment. These strategies include antibodies that re-educate tumor macrophages, vaccines that introduce tumor-specific dendritic cells, checkpoint molecule inhibition, engineered T cells, and proteins that help T cells engage directly with tumor cells. Despite this, there is still much ground to be gained in improving the response rates of the various immunotherapies currently being trialed. Through historical and contemporary studies, we examine the fundamentals of CNS immunity that shape how to approach immune modulation in GBM, including the now revamped concept of CNS privilege. We also discuss the preclinical models used to study GBM progression and immunity. Lastly, we discuss the immunotherapeutic strategies currently being studied to help overcome the hurdles of the blood–brain barrier and the immunosuppressive tumor microenvironment.
topic CNS immunity
tumor microenvironment
glioblastoma
immunotherapy
url https://www.mdpi.com/1422-0067/21/19/7358
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