Hypoplastic myelodysplastic syndromes can be distinguished from acquired aplastic anaemia by bone marrow stem cell expression of the tumour necrosis factor receptor

Br J Haematol. 2002 Jul;118(1):181-8. doi: 10.1046/j.1365-2141.2002.03592.x.

Abstract

It is often difficult to distinguish hypoplastic myelodysplastic syndrome (h-MDS) from acquired aplastic anaemia (AA), because of the considerable clinical, cytological and histological similarities between these two disorders. The distinction between AA and h-MDS is important because there is a higher risk of progression to acute leukaemia in patients with h-MDS compared with AA. Recent studies suggest that tumour necrosis factor-alpha (TNF-alpha) plays an important role in the development of AA. In order to determine the potential importance of TNF-alpha in the differential diagnosis of hypoplastic bone marrow (BM) disorders, we examined whether analysis ofTNF-receptor expression could be used as a tool to differentiate AA from h-MDS. Flow cytometric analysis revealed that BM stem cells (CD34+) from AA patients have markedly greater TNF receptor (R) 1 and TNFR2 expression than those from patients with MDS and h-MDS. We suggest that the BM stem cells with a high expression of TNFR in patients with AA may be potently sensitive to TNF-alpha stimulation of differentiation. Thus, we propose that quantification of TNFR expression in BM stem cellsmay be a useful method to distinguish AA from h-MDS.

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Anemia, Aplastic / diagnosis*
  • Anemia, Aplastic / immunology
  • Anemia, Aplastic / metabolism
  • Antigens, CD / analysis
  • Antigens, CD34*
  • Biomarkers / analysis
  • Diagnosis, Differential
  • Female
  • Flow Cytometry
  • Humans
  • Leukemia, Myeloid / drug therapy
  • Leukemia, Myeloid / metabolism
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / diagnosis*
  • Myelodysplastic Syndromes / immunology
  • Myelodysplastic Syndromes / metabolism
  • Receptors, Tumor Necrosis Factor / analysis*
  • Receptors, Tumor Necrosis Factor, Type II
  • Stem Cells / immunology
  • Stem Cells / metabolism*

Substances

  • Antigens, CD
  • Antigens, CD34
  • Biomarkers
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type II