Identification of a novel dendritic cell-like subset of CD64(+) / CD16(+) blood monocytes

Eur J Immunol. 2001 Jan;31(1):48-56. doi: 10.1002/1521-4141(200101)31:1<48::aid-immu48>3.0.co;2-5.

Abstract

Human monocytes (Mo) consist of a major subset of Fcgamma-receptor I (CD64)-positive typical low accessory phagocytes, and a minor CD64(-) DC-like subset with high T cell-accessory and IFN-alpha-releasing activity. Both populations also differentially express CD16 (Fcgamma-receptor III). Double labeling with anti-CD64 and anti-CD16 mAb, as performed here, identified four different subsets. The CD64(-) subset consists of CD64(-) / 16(+) cells with high antigen-presenting cell (APC) function and macrophage-like phenotype, and a CD64(-) / 16(-) subset of less active APC but which exhibits a higher mixed lymphocyte reaction (MLR) stimulating and IFN-alpha-producing capacity, possibly resembling plasmacytoid dendritic cell type II (DC2) blood precursors. As well as the majority of CD64(+) cells that appeared CD64(+) / 16(-) and represent typical low-accessory, CD14(high) Mo, we could identify and describe a novel minor subset of CD64(+) / 16(+) cells which is unique in combining typical DC and Mo characteristics in the same cell. These are high IL-12 production, high accessory capacity for antigen- or allogen-activated lymphocytes, and high expression of HLA-DR, CD86, and CD11c.

MeSH terms

  • Antigen-Presenting Cells / physiology
  • Cell Separation
  • Cells, Cultured
  • Dendritic Cells / physiology*
  • Humans
  • Immunophenotyping
  • Interferon-alpha / biosynthesis
  • Lipopolysaccharides / pharmacology
  • Monocytes / physiology*
  • Receptors, IgG / analysis*

Substances

  • Interferon-alpha
  • Lipopolysaccharides
  • Receptors, IgG