Identification of P-selectin glycoprotein ligand-1 as a useful marker in acute myeloid leukaemias

János Kappelmayer, Attila Kiss, Éva Karászi, Anikó Veszprémi, János Jakó, Csongor Kiss

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24 Citations (Scopus)


Immunophenotyping is considered to be less valuable in the diagnosis of acute myeloid leukaemias (AML) compared with acute lymphoid leukaemias. Here, we present data on the use of quantitative flow cytometry (QFC) of P-selectin glycoprotein ligand 1 (PSGL-1, CD162) and three-colour immunophenotyping including CD162 staining in the identification of myeloid precursors in AML. Analysis of normal peripheral blood (n = 20) and normal bone marrow (n = 5) samples and on 20 samples from de novo M1, M2, M4 and M5 AML patients demonstrated that PSGL-1 is differentially expressed on various mature and immature leucocyte subsets. It was found by QFC that neutrophils expressed 26500 ± 4500 and monocytes 47200 ± 9900 copies of PSGL-1 on their surface, whereas AML blasts from M1 and M2 AML patients expressed significantly less PSGL-1 (12 000 ± 5300) than mature neutrophils (P < 0.001). In M4 and M5 leukaemias, however, the amount of PSGL-1 on monocytic precursors is displayed in a fairly broad range that is not significantly different from that of mature monocytes (P = 0.084). Using three-colour immunophenotyping PSGL-1-dim staining was co-expressed with CD7 and C34 positivity and PSGL-1 staining intensity on immature myeloid cells paralleled with CD45 expression. This would imply a differential expression of PSGL-1 during myeloid haematopoietic development and suggests that quantification of surface PSGL-1 may aid in differentiating myeloblasts from monoblasts by immunophenotyping in different AML subsets.

Original languageEnglish
Pages (from-to)903-909
Number of pages7
JournalBritish Journal of Haematology
Issue number4
Publication statusPublished - Dec 1 2001


  • Monoblast
  • Myeloblast
  • PSGL-1
  • Quantitative flow cytometry

ASJC Scopus subject areas

  • Hematology

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