Plasmacytoid dendritic cell-derived IFN-alpha induces TNF-related apoptosis-inducing ligand/Apo-2L-mediated antitumor activity by human monocytes following CpG oligodeoxynucleotide stimulation

J Immunol. 2003 Jul 1;171(1):212-8. doi: 10.4049/jimmunol.171.1.212.

Abstract

Immunostimulatory oligodeoxynucleotides (ODN) containing the CpG motif are being tested as immune adjuvants in many disease settings. Of the human PBMC examined, plasmacytoid dendritic cells (pDC) are a major source of type I IFN upon stimulation with CpG ODN. IFNs have numerous immunostimulatory effects, including the induction of TNF-related apoptosis-inducing ligand (TRAIL)/Apo-2L on monocytes, NK cells, and T cells. Importantly, IFN has also been linked to antitumor responses. Thus, we tested whether CpG ODN stimulation of PBMC led to TRAIL/Apo-2L-induced tumor cell death. When PBMC were stimulated with CpG ODN, TRAIL/Apo-2L-dependent tumor cell death was observed. Further examination of CpG ODN-stimulated PBMC revealed that TRAIL/Apo-2L expression was limited to CD14(+) cells, which, when depleted, led to a loss of the TRAIL/Apo-2L-mediated tumor cell killing. Moreover, pDC depletion also abolished the TRAIL/Apo-2L-mediated killing of tumor cell targets. Analysis of the pDC showed IFN-alpha production after CpG ODN stimulation. Finally, inclusion of neutralizing IFN-alpha antiserum with the PBMC during CpG ODN stimulation abrogated TRAIL/Apo-2L-mediated tumor cell killing. These results define a mechanism by which CpG ODN induces TRAIL/Apo-2L-dependent killing of tumor cells by CD14(+) PBMC, in which CpG ODN-activated pDC produce IFN-alpha that stimulates CD14(+) PBMC to express functional TRAIL/Apo-2L.

Publication types

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

MeSH terms

  • Antineoplastic Agents / blood*
  • Antineoplastic Agents / pharmacology
  • Apoptosis / immunology
  • Apoptosis Regulatory Proteins
  • Cells, Cultured
  • CpG Islands / immunology*
  • Cytotoxicity Tests, Immunologic
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Humans
  • Interferon-alpha / biosynthesis
  • Interferon-alpha / blood
  • Interferon-alpha / physiology*
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Ligands
  • Lipopolysaccharide Receptors / biosynthesis
  • Macrophages / immunology
  • Macrophages / metabolism
  • Melanoma / immunology
  • Melanoma / pathology
  • Melanoma / therapy
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / blood
  • Membrane Glycoproteins / physiology*
  • Monocytes / immunology*
  • Monocytes / metabolism
  • Oligodeoxyribonucleotides / pharmacology*
  • Plasma Cells / immunology*
  • Plasma Cells / metabolism
  • TNF-Related Apoptosis-Inducing Ligand
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • Antineoplastic Agents
  • Apoptosis Regulatory Proteins
  • CPG-oligonucleotide
  • Interferon-alpha
  • Ligands
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • Oligodeoxyribonucleotides
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • Tumor Necrosis Factor-alpha