Identification of a leukemic counterpart of the plasmacytoid dendritic cells

Blood. 2001 May 15;97(10):3210-7. doi: 10.1182/blood.v97.10.3210.

Abstract

This work aims to demonstrate that CD4(+)CD56(+) malignancies arise from transformed cells of the lymphoid-related plasmacytoid dendritic cell (pDC) subset. The analysis of malignant cells from 7 patients shows that in all cases, like pDCs, leukemic cells are negative for lineage markers CD3, CD19, CD13, CD33, and CD11c but express high levels of interleukin-3 receptor alpha chain (IL-3Ralpha), HLA-DR, and CD45RA. Tumor cells produce interferon-alpha in response to influenza virus, while upon maturation with IL-3 they become a powerful inducer of naive CD4(+) T-cell proliferation and promote their T-helper 2 polarization. As pDCs, leukemic cells also express pre-Talpha and lambda-like 14.1 transcripts, arguing in favor of a lymphoid origin. In addition, malignant cells express significant levels of CD56 and granzyme B. Overall, those observations suggest that CD4(+)CD56(+) leukemic cells could represent the malignant counterpart of pDCs, both of which are closely related to B, T, and NK cells.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • CD4 Antigens / analysis
  • CD40 Antigens / genetics
  • CD40 Antigens / physiology
  • CD56 Antigen / analysis
  • Cell Differentiation
  • Child
  • Dendritic Cells / immunology
  • Dendritic Cells / pathology*
  • Female
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Granzymes
  • HLA-DR Antigens / analysis
  • Humans
  • Interferon-alpha / biosynthesis
  • Interleukin-3 / pharmacology
  • Leukemia / immunology
  • Leukemia / pathology*
  • Leukocyte Common Antigens / analysis
  • Male
  • Middle Aged
  • Receptors, Interleukin-3 / analysis
  • Serine Endopeptidases / analysis
  • T-Lymphocytes / immunology
  • T-Lymphocytes, Helper-Inducer / immunology
  • Transfection
  • Tumor Cells, Cultured

Substances

  • CD4 Antigens
  • CD40 Antigens
  • CD56 Antigen
  • HLA-DR Antigens
  • Interferon-alpha
  • Interleukin-3
  • Receptors, Interleukin-3
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Leukocyte Common Antigens
  • GZMB protein, human
  • Granzymes
  • Serine Endopeptidases