Oncolytic vaccinia virus immunotherapy antagonizes image-guided radiotherapy in mouse mammary tumor models

PLoS One. 2024 Mar 18;19(3):e0298437. doi: 10.1371/journal.pone.0298437. eCollection 2024.

Abstract

Ionizing radiation (IR) and oncolytic viruses are both used to treat cancer, and the effectiveness of both agents depends upon stimulating an immune response against the tumor. In this study we tested whether combining image guided ionizing radiation (IG-IR) with an oncolytic vaccinia virus (VACV) could yield a better therapeutic response than either treatment alone. ΔF4LΔJ2R VACV grew well on irradiated human and mouse breast cancer cells, and the virus can be combined with 4 or 8 Gy of IR to kill cells in an additive or weakly synergistic manner. To test efficacy in vivo we used immune competent mice bearing orthotopic TUBO mammary tumors. IG-IR worked well with 10 Gy producing 80% complete responses, but this was halved when the tumors were treated with VACV starting 2 days after IG-IR. VACV monotherapy was ineffective in this model. The antagonism was time dependent as waiting for 21 days after IG-IR eliminated the inhibitory effect but without yielding any further benefits over IR alone. In irradiated tumors, VACV replication was also lower, suggesting that irradiation created an environment that did not support infection as well in vivo as in vitro. A study of how four different treatment regimens affected the immune composition of the tumor microenvironment showed that treating irradiated tumors with VACV altered the immunological profiles in tumors exposed to IR or VACV alone. We detected more PD-1 and PD-L1 expression in tumors exposed to IR+VACV but adding an αPD-1 antibody to the protocol did not change the way VACV interferes with IG-IR therapy. VACV encodes many immunosuppressive gene products that may interfere with the ability of radiotherapy to induce an effective anti-tumor immune response through the release of danger-associated molecular patterns. These data suggest that infecting irradiated tumors with VACV, too soon after exposure, may interfere in the innate and linked adaptive immune responses that are triggered by radiotherapy to achieve a beneficial impact.

MeSH terms

  • Animals
  • Humans
  • Immunotherapy
  • Mammary Neoplasms, Animal* / radiotherapy
  • Mice
  • Oncolytic Virotherapy* / methods
  • Oncolytic Viruses* / genetics
  • Radiotherapy, Image-Guided*
  • Tumor Microenvironment
  • Vaccinia virus / genetics
  • Vaccinia*

Grants and funding

This research was funded by grants to DHE, MMH, and R. Moore from the Canadian Institutes of Health Research (CIHR MOP 130473 and BOG 25964; https://cihr-irsc.gc.ca/e/193.html), the Canadian Breast Cancer Foundation/Canadian Cancer Society to MMH, DHE, and D. Murray (#300066; https://cancer.ca/en/) and the University of Alberta’s Li Ka Shing Institute for Virology. BU gratefully acknowledges scholarships from the CIHR (DRA 157828), Alberta Innovates Health Solutions (GS 201600021; https://albertainnovates.ca/), and the Alberta Cancer Foundation (ACF 26536; https://www.albertacancer.ca/). The SARRP irradiator was funded by award #31313 to DHE, D. Murray, and D. Eisenstat from the Canadian Foundation for Innovation; https://www.innovation.ca/) and Alberta Innovates. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.