Non-oncogenic Acute Viral Infections Disrupt Anti-cancer Responses and Lead to Accelerated Cancer-Specific Host Death

Cell Rep. 2016 Oct 18;17(4):957-965. doi: 10.1016/j.celrep.2016.09.068.

Abstract

In light of increased cancer prevalence and cancer-specific deaths in patients with infections, we investigated whether infections alter anti-tumor immune responses. We report that acute influenza infection of the lung promotes distal melanoma growth in the dermis and leads to accelerated cancer-specific host death. Furthermore, we show that during influenza infection, anti-melanoma CD8+ T cells are shunted from the tumor to the infection site, where they express high levels of the inhibitory receptor programmed cell death protein 1 (PD-1). Immunotherapy to block PD-1 reverses this loss of anti-tumor CD8+ T cells from the tumor and decreases infection-induced tumor growth. Our findings show that acute non-oncogenic infection can promote cancer growth, raising concerns regarding acute viral illness sequelae. They also suggest an unexpected role for PD-1 blockade in cancer immunotherapy and provide insight into the immune response when faced with concomitant challenges.

Keywords: CD8(+) T cells; PD-1; breast cancer; cancer; concomitant; infection; influenza; melanoma; mouse; viral.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Proliferation
  • Lung / pathology
  • Melanoma / immunology*
  • Melanoma / pathology*
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Oncogenes*
  • Orthomyxoviridae Infections / pathology*
  • Programmed Cell Death 1 Receptor / metabolism

Substances

  • Programmed Cell Death 1 Receptor