Fig. 5
From: NG2 antigen is a therapeutic target for MLL-rearranged B-cell acute lymphoblastic leukemia

In vivo treatment with 7.1 MoAb sensitizes blasts to VxL, rendering higher CR rates and higher EFS in preclinical PDX models of MLLr-B-ALL. a Monitoring levels of leukemic grafts in PB and BM for the indicated treatments. PB engraftment was analyzed weekly. BM leukemic engraftment was analyzed using BM aspirates at the end of VxL ± 7.1 MoAb treatment (day 15) and at the end of follow-up period (day 50). Each line represents the same mouse before and after treatment. b Levels of leukemia engraftment in BM at treatment initiation (day 0) for VxL or VxL ± 7.1 MoAb mice cohorts. c BM levels of MRD at the end of two cycles of VxL ± 7.1 MoAb (day 15). Each dot represents a single mouse. A mouse is considered in CR when the % of blasts in BM <1% (blue horizontal dotted line). The light blue bars represent the proportion of mice in CR (right Y-axis) for VxL and VxL ± 7.1 MoAb. d Kaplan–Meier survival curves for 45 days EFS (n = 10–11 mice in each group). *p < 0.05; n.s.: no significant differences