Expansion of donor-reactive host T cells in primary graft failure after allogeneic hematopoietic SCT following reduced-intensity conditioning

Bone Marrow Transplant. 2014 Jan;49(1):110-5. doi: 10.1038/bmt.2013.134. Epub 2013 Sep 9.

Abstract

Graft rejection remains a major obstacle in allogeneic hematopoietic SCT following reduced-intensity conditioning (RIC-SCT), particularly after cord blood transplantation (CBT). In a murine MHC-mismatched model of RIC-SCT, primary graft rejection was associated with activation and expansion of donor-reactive host T cells in peripheral blood and BM early after SCT. Donor-derived dendritic cells are at least partly involved in host T-cell activation. We then evaluated if such an expansion of host T cells could be associated with graft rejection after RIC-CBT. Expansion of residual host lymphocytes was observed in 4/7 patients with graft rejection at 3 weeks after CBT, but in none of the 17 patients who achieved engraftment. These results suggest the crucial role of residual host T cells after RIC-SCT in graft rejection and expansion of host T cells could be a marker of graft rejection. Development of more efficient T cell-suppressive conditioning regimens may be necessary in the context of RIC-SCT.

MeSH terms

  • Adult
  • Aged
  • Animals
  • Chimerism
  • Female
  • Graft Rejection / immunology*
  • Graft vs Host Disease / immunology
  • Hematopoietic Stem Cell Transplantation / methods*
  • Humans
  • Lymphocytes / cytology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Models, Animal
  • Retrospective Studies
  • Risk
  • T-Lymphocytes / immunology*
  • T-Lymphocytes, Cytotoxic / cytology
  • Transplantation Conditioning / methods*
  • Transplantation, Homologous
  • Young Adult