Abstract

Oncolytic viruses (OVs) are potent anti-cancer biologics with a bright future, having substantial evidence of efficacy in patients with cancer. Bi- and tri-specific antibodies targeting tumor antigens and capable of activating T cell receptor signaling have also shown great promise in cancer immunotherapy. In a cutting-edge strategy, investigators have incorporated the two independent anti-cancer modalities, transforming them into bi- or tri-specific T cell engager (BiTE or TriTE)-armed OVs for targeted immunotherapy. Since 2014, multiple research teams have studied this combinatorial strategy, and it showed substantial efficacy in various tumor models. Here, we first provide a brief overview of the current status of oncolytic virotherapy and the use of multi-specific antibodies for cancer immunotherapy. We then summarize progress on BiTE and TriTE antibodies as a novel class of cancer therapeutics in preclinical and clinical studies, followed by a discussion of BiTE- or TriTE-armed OVs for cancer therapy in translational models. In addition, T cell receptor mimics (TCRm) have been developed into BiTEs and are expected to greatly expand the application of BiTEs and BiTE-armed OVs for the effective targeting of intracellular tumor antigens. Future applications of such innovative combination strategies are emerging as precision cancer immunotherapies.

Highlights

  • Oncolytic viruses (OVs) are versatile and increasingly effective anticancer agents [1,2,3]

  • Recent findings related to OVs armed with various bispecific T cell engager antibody (BiTE) antibodies for cancer immunotherapy will be reviewed

  • The results showed that overall survival was significantly longer in the treatment group

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Summary

Introduction

Oncolytic viruses (OVs) are versatile and increasingly effective anticancer agents [1,2,3]. OVs modulate the tumor microenvironment (TME), resulting in augmentation of both local and systemic antitumor immunity. This is extremely important as systemic immunity is required for effective cancer immunotherapy in the setting of multi-focal, metastatic disease [7]. Recombinant OVs can recondition the TME, facilitating entry, and they can sustain therapeutic functionality of tumor-infiltrating lymphocytes [19,20,21] in concert with antigen-crosspresenting dendritic cells and lymphatic vessel engagement [22,23], in association with improving antitumor efficacy. Recent findings related to OVs armed with various BiTE antibodies for cancer immunotherapy will be reviewed

Oncolytic Virus-Mediated Immunotherapy
BiTE- and TriTE-Armed OVs Mediate Superior Therapeutic Efficacy
Conclusions and Perspectives

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