Viral Control of Glioblastoma

Glioblastoma multiforme (GBM) is a universally lethal cancer of the central nervous system. Patients with GBM have a median survival of 14 months and a 5-year survival of less than 5%, a grim statistic that has remained unchanged over the last 50 years. GBM is intransigent for a variety of reasons....

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Main Authors: Nicole Mihelson, Dorian B. McGavern
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/7/1264
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spelling doaj-2e32d954aeed4d109102be9081014f062021-07-23T14:11:21ZengMDPI AGViruses1999-49152021-06-01131264126410.3390/v13071264Viral Control of GlioblastomaNicole Mihelson0Dorian B. McGavern1Viral Immunology & Intravital Imaging Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, Room 5N240C, Bethesda, MD 20892, USAViral Immunology & Intravital Imaging Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, Room 5N240C, Bethesda, MD 20892, USAGlioblastoma multiforme (GBM) is a universally lethal cancer of the central nervous system. Patients with GBM have a median survival of 14 months and a 5-year survival of less than 5%, a grim statistic that has remained unchanged over the last 50 years. GBM is intransigent for a variety of reasons. The immune system has a difficult time mounting a response against glioblastomas because they reside in the brain (an immunologically dampened compartment) and generate few neoantigens relative to other cancers. Glioblastomas inhabit the brain like sand in the grass and display a high degree of intra- and inter-tumoral heterogeneity, impeding efforts to therapeutically target a single pathway. Of all potential therapeutic strategies to date, virotherapy offers the greatest chance of counteracting each of the obstacles mounted by GBM. Virotherapy can xenogenize a tumor that is deft at behaving like “self”, triggering adaptive immune recognition in an otherwise immunologically quiet compartment. Viruses can also directly lyse tumor cells, creating damage and further stimulating secondary immune reactions that are detrimental to tumor growth. In this review, we summarize the basic immune mechanisms underpinning GBM immune evasion and the recent successes achieved using virotherapies.https://www.mdpi.com/1999-4915/13/7/1264glioblastoma multiformeimmune evasionvirotherapiesimmunotherapeutic strategies
collection DOAJ
language English
format Article
sources DOAJ
author Nicole Mihelson
Dorian B. McGavern
spellingShingle Nicole Mihelson
Dorian B. McGavern
Viral Control of Glioblastoma
Viruses
glioblastoma multiforme
immune evasion
virotherapies
immunotherapeutic strategies
author_facet Nicole Mihelson
Dorian B. McGavern
author_sort Nicole Mihelson
title Viral Control of Glioblastoma
title_short Viral Control of Glioblastoma
title_full Viral Control of Glioblastoma
title_fullStr Viral Control of Glioblastoma
title_full_unstemmed Viral Control of Glioblastoma
title_sort viral control of glioblastoma
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2021-06-01
description Glioblastoma multiforme (GBM) is a universally lethal cancer of the central nervous system. Patients with GBM have a median survival of 14 months and a 5-year survival of less than 5%, a grim statistic that has remained unchanged over the last 50 years. GBM is intransigent for a variety of reasons. The immune system has a difficult time mounting a response against glioblastomas because they reside in the brain (an immunologically dampened compartment) and generate few neoantigens relative to other cancers. Glioblastomas inhabit the brain like sand in the grass and display a high degree of intra- and inter-tumoral heterogeneity, impeding efforts to therapeutically target a single pathway. Of all potential therapeutic strategies to date, virotherapy offers the greatest chance of counteracting each of the obstacles mounted by GBM. Virotherapy can xenogenize a tumor that is deft at behaving like “self”, triggering adaptive immune recognition in an otherwise immunologically quiet compartment. Viruses can also directly lyse tumor cells, creating damage and further stimulating secondary immune reactions that are detrimental to tumor growth. In this review, we summarize the basic immune mechanisms underpinning GBM immune evasion and the recent successes achieved using virotherapies.
topic glioblastoma multiforme
immune evasion
virotherapies
immunotherapeutic strategies
url https://www.mdpi.com/1999-4915/13/7/1264
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