Multi-modal Potentiation of Oncolytic Virotherapy by Vanadium Compounds

Mol Ther. 2018 Jan 3;26(1):56-69. doi: 10.1016/j.ymthe.2017.10.014. Epub 2017 Oct 24.

Abstract

Oncolytic viruses (OV) are an emerging class of anticancer bio-therapeutics that induce antitumor immunity through selective replication in tumor cells. However, the efficacy of OVs as single agents remains limited. We introduce a strategy that boosts the therapeutic efficacy of OVs by combining their activity with immuno-modulating, small molecule protein tyrosine phosphatase inhibitors. We report that vanadium-based phosphatase inhibitors enhance OV infection in vitro and ex vivo, in resistant tumor cell lines. Furthermore, vanadium compounds increase antitumor efficacy in combination with OV in several syngeneic tumor models, leading to systemic and durable responses, even in models otherwise refractory to OV and drug alone. Mechanistically, this involves subverting the antiviral type I IFN response toward a death-inducing and pro-inflammatory type II IFN response, leading to improved OV spread, increased bystander killing of cancer cells, and enhanced antitumor immune stimulation. Overall, we showcase a new ability of vanadium compounds to simultaneously maximize viral oncolysis and systemic anticancer immunity, offering new avenues for the development of improved immunotherapy strategies.

Keywords: CXCL9; STAT; T cell activation; VSV; immunotherapy; oncolytic virus; type I interferon; type II interferon; vanadate; vanadium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Chemokine CXCL9 / metabolism
  • Combined Modality Therapy
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Genetic Therapy / methods
  • Genetic Vectors / genetics*
  • Humans
  • Immunotherapy
  • Inflammation Mediators / metabolism
  • Interferon Type I / metabolism
  • Interferon-gamma / metabolism
  • Lymphocyte Activation / immunology
  • Mice
  • Mortality
  • Oncolytic Virotherapy*
  • Oncolytic Viruses / genetics*
  • Reactive Oxygen Species / metabolism
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • Vanadium Compounds / pharmacology*
  • Xenograft Model Antitumor Assays

Substances

  • Biomarkers
  • Chemokine CXCL9
  • Cytokines
  • Inflammation Mediators
  • Interferon Type I
  • Reactive Oxygen Species
  • Vanadium Compounds
  • Interferon-gamma

Grants and funding