Targeting myeloid-derived suppressor cells with colony stimulating factor-1 receptor blockade can reverse immune resistance to immunotherapy in indoleamine 2,3-dioxygenase-expressing tumors

EBioMedicine. 2016 Apr:6:50-58. doi: 10.1016/j.ebiom.2016.02.024. Epub 2016 Feb 13.

Abstract

Tumor indoleamine 2,3-dioxygenase (IDO) promotes immunosuppression by direct action on effector T cells and Tregs and through recruitment, expansion and activation of myeloid-derived suppressor cells (MDSCs). Targeting of MDSCs is clinically being explored as a therapeutic strategy, though optimal targeting strategies and biomarkers predictive of response are presently unknown. Maturation and tumor recruitment of MDSCs are dependent on signaling through the receptor tyrosine kinase CSF-1R on myeloid cells. Here, we show that MDSCs are the critical cell population in IDO-expressing B16 tumors in mediating accelerated tumor outgrowth and resistance to immunotherapy. Using a clinically relevant drug, we show that inhibition of CSF-1R signaling can functionally block tumor-infiltrating MDSCs and enhance anti-tumor T cell responses. Furthermore, inhibition of CSF-1R sensitizes IDO-expressing tumors to immunotherapy with T cell checkpoint blockade, and combination of CSF-1R blockade with IDO inhibitors potently elicits tumor regression. These findings provide evidence for a critical and functional role for MDSCs on the in vivo outcome of IDO-expressing tumors.

Keywords: CSF-1R; CTLA-4; IDO; Immunotherapy; MDSCs; PD-1.

MeSH terms

  • Animals
  • CTLA-4 Antigen / administration & dosage
  • Cell Line, Tumor
  • Colonic Neoplasms / drug therapy*
  • Colonic Neoplasms / metabolism
  • Drug Resistance, Neoplasm / drug effects
  • Drug Synergism
  • Enzyme Inhibitors / administration & dosage
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Immunotherapy / methods*
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / antagonists & inhibitors
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism*
  • Melanoma, Experimental / drug therapy*
  • Melanoma, Experimental / metabolism
  • Mice
  • Molecular Targeted Therapy
  • Myeloid-Derived Suppressor Cells / drug effects*
  • Programmed Cell Death 1 Receptor / administration & dosage
  • Receptor, Macrophage Colony-Stimulating Factor / antagonists & inhibitors*
  • Xenograft Model Antitumor Assays

Substances

  • CTLA-4 Antigen
  • Enzyme Inhibitors
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Programmed Cell Death 1 Receptor
  • Receptor, Macrophage Colony-Stimulating Factor