Figure 1.
Validity of high-resolution flow cytometry. (A) An example of analysis on a patient with PNH+ AA is shown. Gates were set up to exclude SSCdim (i) and CD11bdim granulocytes and glycophorin Adim RBCs (ii,v). Cells within rectangles showing horizontal distribution represent PNH-type cells. (B) RBCs from a healthy individual and a patient with AA were examined using a low-resolution assay and the high-resolution assay. Numbers on histograms denote the percentages of CD55-CD59- cells in total RBCs for the low-resolution assay, and in glycophorin A+ RBCs for the high-resolution assay. (C) RBCs from a patient with PNH+ AA were incubated in acidified saline containing heat-inactivated or untreated serum. CD55-CD59- RBCs were then quantified. (D) PNH+ AA WBCs were incubated with or without 0.5 × 10-8 M aerolysin and analyzed by flow cytometry.

Validity of high-resolution flow cytometry. (A) An example of analysis on a patient with PNH+ AA is shown. Gates were set up to exclude SSCdim (i) and CD11bdim granulocytes and glycophorin Adim RBCs (ii,v). Cells within rectangles showing horizontal distribution represent PNH-type cells. (B) RBCs from a healthy individual and a patient with AA were examined using a low-resolution assay and the high-resolution assay. Numbers on histograms denote the percentages of CD55-CD59- cells in total RBCs for the low-resolution assay, and in glycophorin A+ RBCs for the high-resolution assay. (C) RBCs from a patient with PNH+ AA were incubated in acidified saline containing heat-inactivated or untreated serum. CD55-CD59- RBCs were then quantified. (D) PNH+ AA WBCs were incubated with or without 0.5 × 10-8 M aerolysin and analyzed by flow cytometry.

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