Origin and subset distribution of peripheral blood dendritic cells in patients with chronic graft-versus-host disease

Transplantation. 2003 Jan 27;75(2):221-5. doi: 10.1097/01.TP.0000041783.34083.11.

Abstract

Background: After allogeneic hematopoietic stem cell transplantation, donor T cells interact with an antigen-presenting cell environment that is distorted in number, level of activation, and origin. The role of antigen presentation in the development of chronic graft-versus host disease (cGVHD) is unknown.

Methods: The number and origin of peripheral blood immature myeloid (CD19- CD1c+) and plasmacytoid (BDCA-2+) dendritic cells (DCs) was determined in 30 patients at more than 100 days after allogeneic hematopoietic stem cell transplantation.

Results: Patients with cGVHD had significantly higher plasmacytoid DC numbers than individuals without this complication (9.1+/-2.0 x 10(6)/L versus 3.8+/-0.6 x 10(6)/L, =0.025). Chimerism studies demonstrated that DCs in patients with cGVHD were exclusively of donor origin, whereas persistence of host DCs was observed in some control patients.

Conclusions: The antigen-presenting cell environment in patients with cGVHD, as represented by immature blood DCs, is of donor origin but distorted in terms of subset distribution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD1 / analysis
  • Antigens, CD19 / analysis
  • Cell Count
  • Chronic Disease
  • Dendritic Cells / immunology*
  • Female
  • Glycoproteins / analysis
  • Graft vs Host Disease / immunology*
  • HLA-DR Antigens / analysis
  • Humans
  • Male
  • Middle Aged

Substances

  • Antigens, CD1
  • Antigens, CD19
  • CD1C protein, human
  • Glycoproteins
  • HLA-DR Antigens