Vaccines (Sep 2018)

BDCA1+CD14+ Immunosuppressive Cells in Cancer, a Potential Target?

  • Thomas J. van Ee,
  • Heleen H. Van Acker,
  • Tom G. van Oorschot,
  • Viggo F. Van Tendeloo,
  • Evelien L. Smits,
  • Ghaith Bakdash,
  • Gerty Schreibelt,
  • I. Jolanda M. de Vries

DOI
https://doi.org/10.3390/vaccines6030065
Journal volume & issue
Vol. 6, no. 3
p. 65

Abstract

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Dendritic cell (DC) vaccines show promising effects in cancer immunotherapy. However, their efficacy is affected by a number of factors, including (1) the quality of the DC vaccine and (2) tumor immune evasion. The recently characterized BDCA1+CD14+ immunosuppressive cells combine both aspects; their presence in DC vaccines may directly hamper vaccine efficacy, whereas, in patients, BDCA1+CD14+ cells may suppress the induced immune response in an antigen-specific manner systemically and at the tumor site. We hypothesize that BDCA1+CD14+ cells are present in a broad spectrum of cancers and demand further investigation to reveal treatment opportunities and/or improvement for DC vaccines. In this review, we summarize the findings on BDCA1+CD14+ cells in solid cancers. In addition, we evaluate the presence of BDCA1+CD14+ cells in leukemic cancers. Preliminary results suggest that the presence of BDCA1+CD14+ cells correlates with clinical features of acute and chronic myeloid leukemia. Future research focusing on the differentiation from monocytes towards BDCA1+CD14+ cells could reveal more about their cell biology and clinical significance. Targeting these cells in cancer patients may improve the outcome of cancer immunotherapy.

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