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Oncolytic viruses as engineering platforms for combination immunotherapy

Nature Reviews Cancervolume 18pages419432 (2018) | Download Citation


To effectively build on the recent successes of immune checkpoint blockade, adoptive T cell therapy and cancer vaccines, it is critical to rationally design combination strategies that will increase and extend efficacy to a larger proportion of patients. For example, the combination of anti-cytotoxic T lymphocyte-associated antigen 4 (CTLA4) and anti-programmed cell death protein 1 (PD1) immune checkpoint inhibitors essentially doubles the response rate in certain patients with metastatic melanoma. However, given the heterogeneity of cancer, it seems likely that even more complex combinations of immunomodulatory agents may be required to obtain consistent, durable therapeutic responses against a broad spectrum of cancers. This carries serious implications in terms of toxicities for patients, feasibility for care providers and costs for health-care systems. A compelling solution is offered by oncolytic viruses (OVs), which can be engineered to selectively replicate within and destroy tumour tissue while simultaneously augmenting antitumour immunity. In this Opinion article, we argue that the future of immunotherapy will include OVs that function as multiplexed immune-modulating platforms expressing factors such as immune checkpoint inhibitors, tumour antigens, cytokines and T cell engagers. We illustrate this concept by following the trials and tribulations of tumour-reactive T cells from their initial priming through to the execution of cytotoxic effector function in the tumour bed. We highlight the myriad opportunities for OVs to help overcome critical barriers in the T cell journey, leading to new synergistic mechanisms in the battle against cancer.

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  • 04 May 2018

    In the online html version of this article, the affiliations for Jessica L. Pettigrew and John C. Bell were not correct. Jessica L. Pettigrew is at the Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada and John C. Bell is at the Center for Innovative Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada. This is correct in the print and PDF versions of the article and has been corrected in the html version.


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K.T.-B. was supported by a postdoctoral fellowship from the Susan G. Komen Foundation. B.H.N. receives support from the British Columbia Cancer Foundation. J.C.B. and B.H.N. receive support from the Canadian Institutes of Health Research, the Canadian Cancer Society Research Institute and The Terry Fox Foundation. J.C.B. also receives funding from the Ontario Institute for Cancer Research.

Reviewer information

Nature Reviews Cancer thanks A. Melcher and the other anonymous reviewer(s) for their contribution to the peer review of this work.

Author information


  1. Trev and Joyce Deeley Research Centre, British Columbia Cancer Agency, Victoria, British Columbia, Canada

    • Kwame Twumasi-Boateng
    • , Y. Y. Eunice Kwok
    •  & Brad H. Nelson
  2. Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada

    • Jessica L. Pettigrew
  3. Center for Innovative Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada

    • John C. Bell
  4. Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario, Canada

    • John C. Bell
  5. Department of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada

    • Brad H. Nelson
  6. Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada

    • Brad H. Nelson


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K.T.-B. and J.L.P. researched the data for the article. All authors provided a substantial contribution to discussions of the content. Y.Y.E.K. drafted figures with input from K.T.-B., B.H.N. and J.C.B. K.T.-B. wrote the initial article and B.H.N., J.C.B. and K.T.-B. reviewed and edited the manuscript before submission.

Competing interests

J.C.B. is co-founder of Turnstone Biologics, a paid consultant for Turnstone Biologics and on the Board of Directors for Turnstone Biologics. K.T.-B., J.L.P., Y.Y.E.K. and B.H.N. declare no competing interests.

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Correspondence to John C. Bell or Brad H. Nelson.

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