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Oncolytic virus and PD-1/PD-L1 blockade combination therapy

Authors Chen CY, Hutzen B, Wedekind MF, Cripe TP

Received 22 February 2018

Accepted for publication 1 May 2018

Published 31 July 2018 Volume 2018:7 Pages 65—77

DOI https://doi.org/10.2147/OV.S145532

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Colin Mak

Peer reviewer comments 2

Editor who approved publication: Dr Faris Farassati


Chun-Yu Chen,1 Brian Hutzen,1 Mary F Wedekind,1,2 Timothy P Cripe1,2

1Department of Pediatrics, Center for Childhood Cancer and Blood Diseases, Nationwide Children’s Hospital, 2Division of Hematology/Oncology/Blood and Marrow Transplantation, Nationwide Children’s Hospital, The Ohio State University, Columbus, OH, USA

Abstract: Oncolytic viruses are lytic for many types of cancers but are attenuated or replication-defective in normal tissues. Aside from tumor lysis, oncolytic viruses can induce host immune responses against cancer cells and may thus be viewed as a form of immunotherapy. Although recent successes with checkpoint inhibitors have shown that enhancing antitumor immunity can be effective, the dynamic nature of the immunosuppressive tumor microenvironment presents significant hurdles to the broader application of these therapies. Targeting one immune-suppressive pathway may not be sufficient to eliminate tumors. Here we focus on the development of the combination of oncolytic virotherapy with checkpoint inhibitors designed to target the programmed cell death protein 1 and programmed cell death ligand 1 signaling axis. We also discuss future directions for the clinical application of this novel combination therapy.

Keywords: cancer, viral oncolysis, immunotherapy, immune checkpoint blockade

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