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Virus-Based Immunotherapy of Glioblastoma

Glioblastoma (GBM) is the most common type of primary brain tumor in adults. Despite recent advances in cancer therapy, including the breakthrough of immunotherapy, the prognosis of GBM patients remains dismal. One of the new promising ways to therapeutically tackle the immunosuppressive GBM microen...

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Detalles Bibliográficos
Autores principales: Martikainen, Miika, Essand, Magnus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407011/
https://www.ncbi.nlm.nih.gov/pubmed/30764570
http://dx.doi.org/10.3390/cancers11020186
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author Martikainen, Miika
Essand, Magnus
author_facet Martikainen, Miika
Essand, Magnus
author_sort Martikainen, Miika
collection PubMed
description Glioblastoma (GBM) is the most common type of primary brain tumor in adults. Despite recent advances in cancer therapy, including the breakthrough of immunotherapy, the prognosis of GBM patients remains dismal. One of the new promising ways to therapeutically tackle the immunosuppressive GBM microenvironment is the use of engineered viruses that kill tumor cells via direct oncolysis and via stimulation of antitumor immune responses. In this review, we focus on recently published results of phase I/II clinical trials with different oncolytic viruses and the new interesting findings in preclinical models. From syngeneic preclinical GBM models, it seems evident that oncolytic virus-mediated destruction of GBM tissue coupled with strong adjuvant effect, provided by the robust stimulation of innate antiviral immune responses and adaptive anti-tumor T cell responses, can be harnessed as potent immunotherapy against GBM. Although clinical testing of oncolytic viruses against GBM is at an early stage, the promising results from these trials give hope for the effective treatment of GBM in the near future.
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spelling pubmed-64070112019-03-21 Virus-Based Immunotherapy of Glioblastoma Martikainen, Miika Essand, Magnus Cancers (Basel) Review Glioblastoma (GBM) is the most common type of primary brain tumor in adults. Despite recent advances in cancer therapy, including the breakthrough of immunotherapy, the prognosis of GBM patients remains dismal. One of the new promising ways to therapeutically tackle the immunosuppressive GBM microenvironment is the use of engineered viruses that kill tumor cells via direct oncolysis and via stimulation of antitumor immune responses. In this review, we focus on recently published results of phase I/II clinical trials with different oncolytic viruses and the new interesting findings in preclinical models. From syngeneic preclinical GBM models, it seems evident that oncolytic virus-mediated destruction of GBM tissue coupled with strong adjuvant effect, provided by the robust stimulation of innate antiviral immune responses and adaptive anti-tumor T cell responses, can be harnessed as potent immunotherapy against GBM. Although clinical testing of oncolytic viruses against GBM is at an early stage, the promising results from these trials give hope for the effective treatment of GBM in the near future. MDPI 2019-02-05 /pmc/articles/PMC6407011/ /pubmed/30764570 http://dx.doi.org/10.3390/cancers11020186 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Martikainen, Miika
Essand, Magnus
Virus-Based Immunotherapy of Glioblastoma
title Virus-Based Immunotherapy of Glioblastoma
title_full Virus-Based Immunotherapy of Glioblastoma
title_fullStr Virus-Based Immunotherapy of Glioblastoma
title_full_unstemmed Virus-Based Immunotherapy of Glioblastoma
title_short Virus-Based Immunotherapy of Glioblastoma
title_sort virus-based immunotherapy of glioblastoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407011/
https://www.ncbi.nlm.nih.gov/pubmed/30764570
http://dx.doi.org/10.3390/cancers11020186
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