Figure 1
From: Expression of the immune checkpoint modulator OX40 indicates poor survival in acute myeloid leukemia

OX40 and OX40L expression on hematopoietic cells. OX40 expression was analyzed on hematopoietic cells by flow cytometry. (a) Gating strategy for two exemplary AML samples is outlined: viable (7-AAD−), singlets, mononuclear cells, blast marker (AML1: CD34+/CD117+. AML2: CD33+) and OX40 or OX40L expression as percentage. The histogram shows the representative OX40/OX40L staining (filled peaks) and the corresponding isotype control (open peaks). (b) OX40 expression on blasts of AML patients are depicted as SFI levels (analyzed patients n = 70, positive patients n = 41) and percentage of OX40 positive blasts (analyzed patients n = 70, positive patients n = 30) (boxplots with min/max whiskers). SFI levels and percentage of positive cells above 1.5 and 10%, respectively, were considered as positive expression (dotted line). (c) OX40L expression on blasts of AML patients are depicted as SFI levels (analyzed patients n = 86, positive patients n = 37) and percentage of OX40 positive blasts (analyzed patients n = 86, positive patients n = 30) (boxplots with min/ max whiskers). (d, e) Correlation between the expression of OX40+ and OX40L+ cells as percentage (d) and SFI (e) (p value and spearmans ρ).