The effect of calcineurin inhibitors and corticosteroids on the differentiation of human dendritic cells

Eur J Immunol. 2000 Jul;30(7):1807-12. doi: 10.1002/1521-4141(200007)30:7<1807::AID-IMMU1807>3.0.CO;2-N.

Abstract

Corticosteroids and the calcineurin inhibitors cyclosporin A (CsA) and FK506 have been studied extensively regarding their effects on T lymphocytes, but their effects on dendritic cells (DC) are relatively unknown. Monocytes are one of the precursors of DC that differentiate into CD14-CD1a+ immature DC upon culture with IL-4 and GM-CSF. The presence of CsA or FK506 during differentiation did not affect DC development. In contrast, the presence of corticosteroids, either dexamethasone (Dex) or prednisolone (Pred), for as little as the first 48 h of culture blocked the generation of immature DC. Dex-DC were unresponsive to signals inducing maturation (CD40 ligand, lipopolysaccharide), as demonstrated by the absence of CD83, CD80/CD86 and HLA-DR up-regulation and their strongly reduced T cell stimulatory capacity. Furthermore, Dex-DC showed a decreased CD40 ligand-induced IL-6 and TNF-alpha production, a complete block in IL-12p40 production, while IL-10 production was unaffected. CsA-DC and FK506-DC showed a partial reduction in the production of TNF-alpha, whereas all other functional activities appeared to be similar to control DC. These data show that, when compared to calcineurin inhibitors, corticosteroids have a unique and profound inhibitory effect on the generation and function of DC.

MeSH terms

  • Antigens, CD / analysis
  • CD40 Ligand
  • Calcineurin Inhibitors*
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Cyclosporine / pharmacology*
  • Dendritic Cells / cytology
  • Dendritic Cells / drug effects*
  • Dendritic Cells / immunology
  • Dexamethasone / pharmacology*
  • Enzyme Inhibitors / pharmacology*
  • Glucocorticoids / pharmacology*
  • Humans
  • Immunophenotyping
  • Immunosuppressive Agents / pharmacology*
  • Interleukin-10 / biosynthesis
  • Interleukin-12 / biosynthesis
  • Interleukin-6 / biosynthesis
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Monocytes / cytology
  • Monocytes / drug effects
  • Monocytes / immunology
  • Prednisolone / pharmacology*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • Tacrolimus / pharmacology*
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Antigens, CD
  • Calcineurin Inhibitors
  • Enzyme Inhibitors
  • Glucocorticoids
  • Immunosuppressive Agents
  • Interleukin-6
  • Membrane Glycoproteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • CD40 Ligand
  • Interleukin-12
  • Dexamethasone
  • Cyclosporine
  • Prednisolone
  • Tacrolimus