Involvement of natural killer cells in patients with myelodysplastic syndrome carrying monosomy 7 revealed by the application of fluorescence in situ hybridization to cells collected by means of fluorescence-activated cell sorting

Br J Haematol. 2000 Sep;110(4):876-9. doi: 10.1046/j.1365-2141.2000.02294.x.

Abstract

Monosomy 7 is the most frequent chromosome abnormality among patients with secondary myelodysplastic syndrome (MDS). We used fluorescence in situ hybridization (FISH) and fluorescence-activated cell sorting (FACS) in order to clarify the lineage involvement. Four patients, three with de novo MDS and one with secondary MDS, were enrolled in this study. Monosomy 7 was observed in pluripotent stem cells (CD34(+)Thy-1(+)), and in B (CD34(+)CD19(+)) and T/natural killer (NK) progenitors (CD34(+)CD7(+)). The number of abnormal cells of B (CD19(+)) and T (CD3(+)) cells was below the cut-off value, but approximately 60% of the NK cells (CD3-CD56(+)) contained monosomy 7 in three of the patients.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antigens, CD34
  • B-Lymphocytes
  • Chromosomes, Human, Pair 7
  • Female
  • Flow Cytometry
  • Hematopoietic Stem Cells / immunology
  • Humans
  • Immunophenotyping
  • In Situ Hybridization, Fluorescence
  • Killer Cells, Natural / immunology*
  • Male
  • Middle Aged
  • Monosomy
  • Myelodysplastic Syndromes / genetics
  • Myelodysplastic Syndromes / immunology*

Substances

  • Antigens, CD34