Figure 5.
Simultaneous targeting of CD33/CLEC12A yields the highest coverage of pediatric AML, including LSCs. (A) Frequency of AML blasts not expressing either of 2 surface molecules as a measure of AML blasts not covered by combinatorial targeting (mean ± SD). The 7 most promising target combinations are presented. (B) Frequency of AML blasts expressing both targets of 7 promising target combinations (mean ± SD). (C-G) CD45dim cells from 21 samples (not all samples were available for this analysis for technical reasons), with the same cell count per sample, were concatenated into 1 .fcs file, and tSNE parameters were calculated using FlowJo X default settings. Consequently, 5 target combinations (CD33/CD38 in panel C, CD33/CLEC12A in panel D, CD33/EMR2 in panel E, CD33/IL3RA in panel F, and CD33/FLT3 in panel G) are illustrated. Additionally, to depict the coverage of AML LSCs, CD34 and CD38 expression patterns are depicted on the same tSNE map (H).

Simultaneous targeting of CD33/CLEC12A yields the highest coverage of pediatric AML, including LSCs. (A) Frequency of AML blasts not expressing either of 2 surface molecules as a measure of AML blasts not covered by combinatorial targeting (mean ± SD). The 7 most promising target combinations are presented. (B) Frequency of AML blasts expressing both targets of 7 promising target combinations (mean ± SD). (C-G) CD45dim cells from 21 samples (not all samples were available for this analysis for technical reasons), with the same cell count per sample, were concatenated into 1 .fcs file, and tSNE parameters were calculated using FlowJo X default settings. Consequently, 5 target combinations (CD33/CD38 in panel C, CD33/CLEC12A in panel D, CD33/EMR2 in panel E, CD33/IL3RA in panel F, and CD33/FLT3 in panel G) are illustrated. Additionally, to depict the coverage of AML LSCs, CD34 and CD38 expression patterns are depicted on the same tSNE map (H).

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