Figure 2.
Figure 2. Flow cytometric detection of LSCs in a patient treated for AML. BM from a patient treated for AML was tested for MRD. Cells with the typical immunophenotype of LSCs had been demonstrated at this patient's presentation: CD34+CD123+CD117+HLA-DR−CD38−. After therapy, sequential gating for the presence of this phenotype was performed and detected 0.02% of these cells. In the scattergram, gate P1 was drawn around agranular cells (low side scatter, SSC) of small size (low forward scatter, FSC). In the blast gate, a second gate (P2) was drawn around cells with CD117 expression (blue dots), whereas the population of red cells in the first gate was CD117−. In the blast cell characterization contour plot, blast cells within the CD117+ cell population were demonstrated by expression of CD123, but negativity for HLA-DR. The small cell cluster with high HLA-DR expression represents some normal stem cells.

Flow cytometric detection of LSCs in a patient treated for AML. BM from a patient treated for AML was tested for MRD. Cells with the typical immunophenotype of LSCs had been demonstrated at this patient's presentation: CD34+CD123+CD117+HLA-DRCD38. After therapy, sequential gating for the presence of this phenotype was performed and detected 0.02% of these cells. In the scattergram, gate P1 was drawn around agranular cells (low side scatter, SSC) of small size (low forward scatter, FSC). In the blast gate, a second gate (P2) was drawn around cells with CD117 expression (blue dots), whereas the population of red cells in the first gate was CD117. In the blast cell characterization contour plot, blast cells within the CD117+ cell population were demonstrated by expression of CD123, but negativity for HLA-DR. The small cell cluster with high HLA-DR expression represents some normal stem cells.

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