Extracorporeal photopheresis efficiently impairs the proinflammatory capacity of human 6-sulfo LacNAc dendritic cells

Transplantation. 2009 Apr 27;87(8):1134-9. doi: 10.1097/TP.0b013e31819e02d4.

Abstract

Background: Extracorporeal photopheresis (ECP) emerged as a promising treatment modality for steroid-refractory graft-versus-host disease (GVHD), which represents a major complication of allogeneic hematopoietic stem-cell transplantation. Dendritic cells (DCs) display an extraordinary capacity to induce T-cell responses and play a crucial role in the initiation and maintainance of GVHD. This study evaluated the direct impact of ECP on the proinflammatory capacity of 6-sulfo LacNAc (slan) DCs, representing a major subpopulation of human blood DCs.

Methods: SlanDCs were isolated from ECP-treated or untreated blood of healthy donors or GVHD patients by immunomagnetic isolation. The maturation of slanDC was determined by flow cytometry. Cytokine production of slanDCs was measured by enzyme-linked immunosorbent assay. SlanDC-mediated T-cell proliferation was evaluated by H-thymidine incorporation. SlanDC-mediated T-cell programming was determined by flow cytometry.

Results: ECP efficiently impairs the spontaneous maturation and secretion of proinflammatory tumor necrosis factor-alpha, interleukin-1beta, and interleukin-12 by slanDCs. Furthermore, ECP markedly inhibits slanDC-induced proliferation of CD4 and CD8 T cells and polarization of naïve CD4 T lymphocytes into Th1 cells.

Conclusions: These novel findings indicate that ECP efficiently impairs the proinflammatory capacity of slanDCs, which may represent an important mechanism for the therapeutic efficiency of ECP in GVHD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ABO Blood-Group System / analysis*
  • ABO Blood-Group System / immunology
  • Amino Sugars / analysis*
  • Carrier Proteins / analysis
  • Carrier Proteins / immunology
  • Dendritic Cells / physiology*
  • Dendritic Cells / radiation effects
  • Humans
  • Immunoblotting
  • Inflammation / physiopathology*
  • Inflammation / prevention & control
  • Membrane Proteins / analysis
  • Membrane Proteins / immunology
  • Photopheresis*
  • Platelet Endothelial Cell Adhesion Molecule-1 / analysis
  • Platelet Endothelial Cell Adhesion Molecule-1 / immunology
  • Proteome
  • von Willebrand Factor / analysis
  • von Willebrand Factor / immunology

Substances

  • 6-sulfo-LacNac
  • ABO Blood-Group System
  • Amino Sugars
  • Carrier Proteins
  • Membrane Proteins
  • PLVAP protein, human
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Proteome
  • von Willebrand Factor