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Open AccessArticle

Oncolytic Reovirus and Immune Checkpoint Inhibition as a Novel Immunotherapeutic Strategy for Breast Cancer

by 1,2,†, 3,4,†, 3,4, 5, 3, 3,4, 4, 3,4 and 3,4,*
1
Department of Pathology and Laboratory Medicine, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada
2
Histocompatibility and Immunogenetics, Calgary Lab Services, 3535 Research Road NW, Calgary, AB T2L 2K8, Canada
3
Department of Oncology, University of Calgary, 1331 29 Street NW, Calgary, AB T2N 4N2, Canada
4
Tom Baker Cancer Centre, 1331 29 Street NW, Calgary, AB T2N 4N2, Canada
5
Faculty of Medicine, University of Toronto, King’s College Circle, Toronto, ON M5S 1A8, Canada
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Received: 17 May 2018 / Revised: 8 June 2018 / Accepted: 8 June 2018 / Published: 15 June 2018
(This article belongs to the Special Issue Oncolytic Virotherapy)
As the current efficacy of oncolytic viruses (OVs) as monotherapy is limited, exploration of OVs as part of a broader immunotherapeutic treatment strategy for cancer is necessary. Here, we investigated the ability for immune checkpoint blockade to enhance the efficacy of oncolytic reovirus (RV) for the treatment of breast cancer (BrCa). In vitro, oncolysis and cytokine production were assessed in human and murine BrCa cell lines following RV exposure. Furthermore, RV-induced upregulation of tumor cell PD-L1 was evaluated. In vivo, the immunocompetent, syngeneic EMT6 murine model of BrCa was employed to determine therapeutic and tumor-specific immune responses following treatment with RV, anti-PD-1 antibodies or in combination. RV-mediated oncolysis and cytokine production were observed following BrCa cell infection and RV upregulated tumor cell expression of PD-L1. In vivo, RV monotherapy significantly reduced disease burden and enhanced survival in treated mice, and was further enhanced by PD-1 blockade. RV therapy increased the number of intratumoral regulatory T cells, which was reversed by the addition of PD-1 blockade. Finally, dual treatment led to the generation of a systemic adaptive anti-tumor immune response evidenced by an increase in tumor-specific IFN-γ producing CD8+ T cells, and immunity from tumor re-challenge. The combination of PD-1 blockade and RV appears to be an efficacious immunotherapeutic strategy for the treatment of BrCa, and warrants further investigation in early-phase clinical trials. View Full-Text
Keywords: oncolytic viruses; reovirus; immune checkpoint inhibition; PD-1; breast cancer; immunotherapy oncolytic viruses; reovirus; immune checkpoint inhibition; PD-1; breast cancer; immunotherapy
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MDPI and ACS Style

Mostafa, A.A.; Meyers, D.E.; Thirukkumaran, C.M.; Liu, P.J.; Gratton, K.; Spurrell, J.; Shi, Q.; Thakur, S.; Morris, D.G. Oncolytic Reovirus and Immune Checkpoint Inhibition as a Novel Immunotherapeutic Strategy for Breast Cancer. Cancers 2018, 10, 205. https://0-doi-org.brum.beds.ac.uk/10.3390/cancers10060205

AMA Style

Mostafa AA, Meyers DE, Thirukkumaran CM, Liu PJ, Gratton K, Spurrell J, Shi Q, Thakur S, Morris DG. Oncolytic Reovirus and Immune Checkpoint Inhibition as a Novel Immunotherapeutic Strategy for Breast Cancer. Cancers. 2018; 10(6):205. https://0-doi-org.brum.beds.ac.uk/10.3390/cancers10060205

Chicago/Turabian Style

Mostafa, Ahmed A.; Meyers, Daniel E.; Thirukkumaran, Chandini M.; Liu, Peter J.; Gratton, Kathy; Spurrell, Jason; Shi, Qiao; Thakur, Satbir; Morris, Don G. 2018. "Oncolytic Reovirus and Immune Checkpoint Inhibition as a Novel Immunotherapeutic Strategy for Breast Cancer" Cancers 10, no. 6: 205. https://0-doi-org.brum.beds.ac.uk/10.3390/cancers10060205

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