Local oncolytic adenovirotherapy produces an abscopal effect via tumor-derived extracellular vesicles

Mol Ther. 2021 Oct 6;29(10):2920-2930. doi: 10.1016/j.ymthe.2021.05.015. Epub 2021 May 21.

Abstract

Extracellular vesicles (EVs) play important roles in various intercellular communication processes. The abscopal effect is an interesting phenomenon in cancer treatment, in which immune activation is generally considered a main factor. We previously developed a telomerase-specific oncolytic adenovirus, Telomelysin (OBP-301), and occasionally observed therapeutic effects on distal tumors after local treatment in immunodeficient mice. In this study, we hypothesized that EVs may be involved in the abscopal effect of OBP-301. EVs isolated from the supernatant of HCT116 human colon carcinoma cells treated with OBP-301 were confirmed to contain OBP-301, and they showed cytotoxic activity (apoptosis and autophagy) similar to OBP-301. In bilateral subcutaneous HCT116 and CT26 tumor models, intratumoral administration of OBP-301 produced potent antitumor effects on tumors that were not directly treated with OBP-301, involving direct mediation by tumor-derived EVs containing OBP-301. This indicates that immune activation is not the main factor in this abscopal effect. Moreover, tumor-derived EVs exhibited high tumor tropism in orthotopic HCT116 rectal tumors, in which adenovirus E1A and adenovirus type 5 proteins were observed in metastatic liver tumors after localized rectal tumor treatment. In conclusion, local treatment with OBP-301 has the potential to produce abscopal effects via tumor-derived EVs.

Keywords: abscopal effect; drug delivery system; exosome; extracellular vesicles; local treatment; oncolytic adenovirus; systemic delivery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Cell Line, Tumor
  • Cell Survival
  • Colonic Neoplasms / therapy*
  • Extracellular Vesicles / transplantation*
  • Extracellular Vesicles / virology
  • HCT116 Cells
  • Humans
  • Liver Neoplasms / secondary*
  • Liver Neoplasms / therapy*
  • Mice
  • Oncolytic Viruses / genetics
  • Viral Tropism
  • Xenograft Model Antitumor Assays