Oncolytic Adenovirus in Cancer Immunotherapy

Tumor-selective replicating “oncolytic” viruses are novel and promising tools for immunotherapy of cancer. However, despite their first success in clinical trials, previous experience suggests that currently used oncolytic virus monotherapies will not be effective enough to achieve complete tumor re...

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Main Authors: Malin Peter, Florian Kühnel
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/11/3354
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spelling doaj-6f00ee33a0ed4fd9b763d54fe5fcdfdc2020-11-25T04:09:44ZengMDPI AGCancers2072-66942020-11-01123354335410.3390/cancers12113354Oncolytic Adenovirus in Cancer ImmunotherapyMalin Peter0Florian Kühnel1Department of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, 30625 Hannover, GermanyDepartment of Gastroenterology, Hepatology, and Endocrinology, Hannover Medical School, 30625 Hannover, GermanyTumor-selective replicating “oncolytic” viruses are novel and promising tools for immunotherapy of cancer. However, despite their first success in clinical trials, previous experience suggests that currently used oncolytic virus monotherapies will not be effective enough to achieve complete tumor responses and long-term cure in a broad spectrum of cancers. Nevertheless, there are reasonable arguments that suggest advanced oncolytic viruses will play an essential role as enablers of multi-stage immunotherapies including established systemic immunotherapies. Oncolytic adenoviruses (oAds) display several features to meet this therapeutic need. oAds potently lyse infected tumor cells and induce a strong immunogenic cell death associated with tumor inflammation and induction of antitumor immune responses. Furthermore, established and versatile platforms of oAds exist, which are well suited for the incorporation of heterologous genes to optimally exploit and amplify the immunostimulatory effect of viral oncolysis. A considerable spectrum of functional genes has already been integrated in oAds to optimize particular aspects of immune stimulation including antigen presentation, T cell priming, engagement of additional effector functions, and interference with immunosuppression. These advanced concepts have the potential to play a promising future role as enablers of multi-stage immunotherapies involving adoptive cell transfer and systemic immunotherapies.https://www.mdpi.com/2072-6694/12/11/3354oncolytic adenoviruscancer immunotherapymulti-stageimmunostimulatoryarming
collection DOAJ
language English
format Article
sources DOAJ
author Malin Peter
Florian Kühnel
spellingShingle Malin Peter
Florian Kühnel
Oncolytic Adenovirus in Cancer Immunotherapy
Cancers
oncolytic adenovirus
cancer immunotherapy
multi-stage
immunostimulatory
arming
author_facet Malin Peter
Florian Kühnel
author_sort Malin Peter
title Oncolytic Adenovirus in Cancer Immunotherapy
title_short Oncolytic Adenovirus in Cancer Immunotherapy
title_full Oncolytic Adenovirus in Cancer Immunotherapy
title_fullStr Oncolytic Adenovirus in Cancer Immunotherapy
title_full_unstemmed Oncolytic Adenovirus in Cancer Immunotherapy
title_sort oncolytic adenovirus in cancer immunotherapy
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2020-11-01
description Tumor-selective replicating “oncolytic” viruses are novel and promising tools for immunotherapy of cancer. However, despite their first success in clinical trials, previous experience suggests that currently used oncolytic virus monotherapies will not be effective enough to achieve complete tumor responses and long-term cure in a broad spectrum of cancers. Nevertheless, there are reasonable arguments that suggest advanced oncolytic viruses will play an essential role as enablers of multi-stage immunotherapies including established systemic immunotherapies. Oncolytic adenoviruses (oAds) display several features to meet this therapeutic need. oAds potently lyse infected tumor cells and induce a strong immunogenic cell death associated with tumor inflammation and induction of antitumor immune responses. Furthermore, established and versatile platforms of oAds exist, which are well suited for the incorporation of heterologous genes to optimally exploit and amplify the immunostimulatory effect of viral oncolysis. A considerable spectrum of functional genes has already been integrated in oAds to optimize particular aspects of immune stimulation including antigen presentation, T cell priming, engagement of additional effector functions, and interference with immunosuppression. These advanced concepts have the potential to play a promising future role as enablers of multi-stage immunotherapies involving adoptive cell transfer and systemic immunotherapies.
topic oncolytic adenovirus
cancer immunotherapy
multi-stage
immunostimulatory
arming
url https://www.mdpi.com/2072-6694/12/11/3354
work_keys_str_mv AT malinpeter oncolyticadenovirusincancerimmunotherapy
AT floriankuhnel oncolyticadenovirusincancerimmunotherapy
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