CpG-A oligonucleotides induce a monocyte-derived dendritic cell-like phenotype that preferentially activates CD8 T cells

J Immunol. 2003 Apr 1;170(7):3468-77. doi: 10.4049/jimmunol.170.7.3468.

Abstract

Human B cells and plasmacytoid dendritic cells recognize CpG motifs within microbial DNA via Toll-like receptor 9. Two functionally distinct types of CpG motif containing oligonucleotides (CpG ODN) have been described, CpG-A and CpG-B. In contrast to CpG-B, CpG-A induces high amounts of type I IFN (IFN-alpha and IFN-beta) in plasmacytoid dendritic cells. In the present study, we examined the effects of CpG-A on human primary monocytes. In PBMC stimulated with CpG-A and GM-CSF, monocytes showed excellent survival, increased in size and granularity, and within 3 days developed a dendritic cell-like phenotype that was characterized by down-regulation of CD14, partial up-regulation of CCR7, and an increased surface expression of costimulatory and Ag-presenting molecules. This effect could be inhibited by a combination of blocking Abs to type I IFN, and no such CpG-A-induced changes were observed in purified monocytes. Although IL-12 production by this dendritic cell-like phenotype required additional stimulation with CD40 ligand, this cell type spontaneously up-regulated IL-15 expression. Consistent with the known effect of IL-15 on effector and memory CD8 T cells, the frequency of CCR7(-)/CD45RA(-) CD8 T cells was selectively increased in allogeneic T cell assays. Furthermore, this dendritic cell type was more potent to support both the generation and the IFN-gamma production of autologous influenza matrix peptide-specific memory CD8 T cells as compared with dendritic cells generated in the presence of GM-CSF and IL-4. In conclusion, monocytes exposed to the cytokine milieu provided by CpG-A rapidly develop a dendritic cell-like phenotype that is well equipped to support CD8 T cell responses.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / virology
  • Cell Differentiation / immunology
  • Cells, Cultured
  • CpG Islands / immunology*
  • Culture Media, Conditioned
  • Dendritic Cells / cytology
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Humans
  • Immunologic Memory
  • Immunophenotyping
  • Influenza A virus / immunology
  • Interferon Type I / physiology
  • Interferon-gamma / biosynthesis
  • Interleukin-15 / biosynthesis
  • Interleukin-4 / pharmacology
  • Leukocyte Common Antigens / biosynthesis
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology*
  • Monocytes / cytology
  • Monocytes / immunology*
  • Monocytes / metabolism
  • Oligodeoxyribonucleotides / immunology
  • Oligodeoxyribonucleotides / pharmacology*
  • Peptide Fragments / immunology
  • Receptors, CCR7
  • Receptors, Chemokine / biosynthesis
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / virology
  • Viral Matrix Proteins / immunology

Substances

  • Adjuvants, Immunologic
  • CCR7 protein, human
  • CPG-oligonucleotide
  • Culture Media, Conditioned
  • Interferon Type I
  • Interleukin-15
  • Oligodeoxyribonucleotides
  • Peptide Fragments
  • Receptors, CCR7
  • Receptors, Chemokine
  • Viral Matrix Proteins
  • influenza matrix peptide (58-66)
  • Interleukin-4
  • Interferon-gamma
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Leukocyte Common Antigens