Cross-Presenting XCR1+ Dendritic Cells as Targets for Cancer Immunotherapy

Cells. 2020 Feb 28;9(3):565. doi: 10.3390/cells9030565.

Abstract

The use of dendritic cells (DCs) to generate effective anti-tumor T cell immunity has garnered much attention over the last thirty-plus years. Despite this, limited clinical benefit has been demonstrated thus far. There has been a revival of interest in DC-based treatment strategies following the remarkable patient responses observed with novel checkpoint blockade therapies, due to the potential for synergistic treatment. Cross-presenting DCs are recognized for their ability to prime CD8+ T cell responses to directly induce tumor death. Consequently, they are an attractive target for next-generation DC-based strategies. In this review, we define the universal classification system for cross-presenting DCs, and the vital role of this subset in mediating anti-tumor immunity. Furthermore, we will detail methods of targeting these DCs both ex vivo and in vivo to boost their function and drive effective anti-tumor responses.

Keywords: DC-based therapy; cancer; cross-presenting dendritic cells; immunotherapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cancer Vaccines / immunology
  • Cross-Priming / immunology*
  • Dendritic Cells / immunology*
  • Humans
  • Immunotherapy*
  • Neoplasms / immunology*
  • Neoplasms / therapy*
  • Receptors, G-Protein-Coupled / metabolism*

Substances

  • Cancer Vaccines
  • Receptors, G-Protein-Coupled