Serum macrophage migration inhibitory factor (MIF) levels after allogeneic hematopoietic stem cell transplantation

Int J Lab Hematol. 2009 Apr;31(2):161-8. doi: 10.1111/j.1751-553X.2007.01016.x. Epub 2007 Dec 12.

Abstract

Macrophage migration inhibitory factor (MIF) may play an important role in the pathogenesis of acute graft-versus-host disease (aGVHD) after allogeneic hematopoietic stem cell transplantation (allo-HSCT), as MIF plays an important role to regulate the production of tumor necrosis factor-alpha (TNF-alpha), one of the inflammatory cytokines which induces and exacerbates aGVHD. We examined the association between serum MIF levels and aGVHD vs. chronic GVHD (cGVHD) in allo-SCT patients in this study. We found a significant increase in the peak serum MIF (14.46 ng +/- 1.47 ng/ml) at onset in patients that developed aGVHD (n = 23, P = 0.009). We also found that mean serum MIF levels in patients who developed extensive type cGVHD within 6 months (12.58 +/- 2.18 ng/ml, n = 13) were significantly higher than MIF levels before allo-HSCT (7.86 +/- 1.17 ng/ml, n = 19, P = 0.04). Therefore, we speculated that serum MIF levels increase during the active phase of both aGVHD and cGVHD.

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Aged
  • Chronic Disease
  • Female
  • Graft vs Host Disease / blood*
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Macrophage Migration-Inhibitory Factors / blood*
  • Male
  • Middle Aged
  • Tumor Necrosis Factor-alpha / blood
  • Young Adult

Substances

  • Macrophage Migration-Inhibitory Factors
  • Tumor Necrosis Factor-alpha