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Updated: Jul 7, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Innate immunity, tumor microenvironment and oncolytic virus therapy: friends or foes?
Marianne M Stanford1, Caroline J Breitbach, John C Bell
1Ottawa Health Research Institute, Centre for Cancer Therapeutics, Ottawa, Ontario, Canada..
Abstract:
The field of oncolytic virus (OV) therapy is an innovative and evolving science, taking advantage of the ability of select viruses to preferentially infect and kill human tumor cells. However, the contribution of the tumor microenvironment, and especially the induced innate immune responses to both the tumor and the virus, has been demonstrated to be a major player in the success of OV therapies. Innate immunity and inflammation in particular can have opposing effects; these can augment OV therapy by enhancing tumor destruction, yet can also recognize and clear the invading virus to significantly hinder viral dissemination through the tumor tissues. This review considers how inflammation and innate immunity impinge on current OV candidates to either facilitate or hinder virotherapy. Novel approaches that modulate or harness the innate immune system to specifically enhance OV-mediated tumor destruction are also discussed.
Insights
Oncolytic virus (OV) therapy shows promise for cancer treatment. This review explores how the immune system
Area of Science:
- Oncolytic virotherapy
- Immunology
- Cancer biology
Background:
- Oncolytic virus (OV) therapy utilizes viruses to selectively infect and destroy cancer cells.
- The tumor microenvironment, particularly innate immune responses, significantly influences OV therapy outcomes.
- Inflammation and innate immunity can both promote tumor destruction and impede viral spread.
Purpose of the Study:
- To review the dual role of inflammation and innate immunity in OV therapy.
- To discuss how these immune components can facilitate or hinder oncolytic virotherapy.
- To explore novel strategies for modulating the immune system to enhance OV efficacy.
Main Methods:
- Literature review of oncolytic virus therapy.
- Analysis of the interplay between innate immunity, inflammation, and OV candidates.
- Discussion of immune-modulatory approaches in virotherapy.
Main Results:
- Innate immunity and inflammation present a complex, often opposing, influence on OV therapy.
- These immune responses can enhance tumor cell lysis but also lead to premature viral clearance.
- Current OV candidates are significantly impacted by these microenvironmental factors.
Conclusions:
- Understanding and manipulating innate immunity and inflammation are crucial for successful OV therapy.
- Novel strategies aim to harness immune responses to improve viral dissemination and tumor targeting.
- Optimizing the host-pathogen-tumor interaction is key to advancing oncolytic virotherapy.
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