Numerical defect of circulating dendritic cell subsets and defective dendritic cell generation from monocytes of patients with advanced melanoma

Cancer Lett. 2013 Sep 1;337(2):184-92. doi: 10.1016/j.canlet.2013.05.013. Epub 2013 May 16.

Abstract

The behaviour of circulating dendritic cells (DCs) and DC generation from monocytes in melanoma patients during the progression of disease have not been described. We report a significant decrease in the absolute number of total DCs, which mainly affects plasmacytoid DCs in stage IV. Additionally, monocyte-DC generation is less efficient in advanced stages, resulting in DCs that exhibit increased phagocytic capacity, potentially indicating a less mature state. These findings elucidate aspects of basic tumour-mediated immunosuppression, which may have implications for immunotherapeutic approaches, suggesting that the selection of patients for immunotherapy should also be made on the basis of their immune status.

Keywords: Circulating dendritic cells; Generation of dendritic cells; Immunotherapy; Melanoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Case-Control Studies
  • Cell Count
  • Cell Shape
  • Cells, Cultured
  • Coculture Techniques
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Dendritic Cells / pathology
  • Dextrans / metabolism
  • Disease Progression
  • Down-Regulation
  • Endocytosis
  • Female
  • Fluorescein-5-isothiocyanate / analogs & derivatives
  • Fluorescein-5-isothiocyanate / metabolism
  • Humans
  • Immunotherapy
  • Lectins, C-Type / metabolism
  • Lymphocyte Activation
  • Lymphocyte Culture Test, Mixed
  • Male
  • Mannose Receptor
  • Mannose-Binding Lectins / metabolism
  • Melanoma / immunology*
  • Melanoma / secondary
  • Melanoma / therapy
  • Middle Aged
  • Monocytes / immunology*
  • Monocytes / metabolism
  • Monocytes / pathology
  • Neoplasm Staging
  • Phagocytosis
  • Phenotype
  • Receptors, Cell Surface / metabolism
  • Skin Neoplasms / immunology*
  • Skin Neoplasms / pathology
  • Skin Neoplasms / therapy
  • T-Lymphocytes / immunology
  • Time Factors
  • Tumor Escape

Substances

  • Dextrans
  • Lectins, C-Type
  • Mannose Receptor
  • Mannose-Binding Lectins
  • Receptors, Cell Surface
  • fluorescein isothiocyanate dextran
  • Fluorescein-5-isothiocyanate