We have studied the expression of cytokine receptors CD25 (IL-2Ra,55kD
), CD116 (hGM-CSRF,145kD), CD117 (CSFR,145kD), CD120a (TNFR,55kD), CD1
20b (TNFR,75kD), CD121a (IL-1R, type I,80kD), CD123 (IL-3R), CD124 (IL
-4R,140kD), CD126 (IL-6R, 80kD), CDw127 (IL-7R, 75kD), CDw128 (IL-8R),
CD130 (gp130 subunit), CD131 (common beta), CD134 (OX40) and also CD9
5 (Fas antigen) on the myeloid leukemic cells. Cells from peripheral b
lood or bone marrow of 30 patients with disorders in myeloid lineage i
ncluded mostly acute myeloid leukemias (with high leukocyte count and
percentage of blasts) were analyzed for the expression of surface memb
rane molecules by indirect immunofluorescence method evaluated by flow
cytometry. The findings indicate that some monoclonal antibodies have
a reactivity against cytokine receptors of pathological cells in indi
vidual cases, but with very variable qualitative and quantitative (num
ber copies/cell) expression (preliminary results). The leukemic cells
demonstrate unique cytokine receptor profiles, which reveal the great
diversity of immunophenotypes within the main functional characterizat
ion of blood malignancies. The immunophenotype heterogeneity of leukem
ic cells has proved to be much greater than to match with existing cla
ssification criteria. This fact could raise the necessity of further e
valuation and specification of cytokine markers of the myeloid acute l
eukemias. On the other hand, detection of cytokine receptors on the le
ukemia cells is important for cytokine therapy.