Figure 6.
Figure 6. CiTE leads to eradication of AML cells in a murine NSG xenograft model without indication of enhanced PD-1 upregulation or body weight loss. (A) Experimental design of mouse studies. (B) Remaining engrafted MOLM-13:PD-L1 (live hCD45+CD33+) cells in BM of exemplary mice per cohort (left) and as mean (right) after 13 days. (C) PD-1 upregulation on human CD45+CD3+CD4+ and CD45+CD3+CD4− T cells. (D) Relative body weight of mice as scored during treatment with CiTE and sctb. Cohorts contained 4 to 6 mice. Error bars in (B-C) indicate standard deviation, in (D) SEM. For statistical analysis, Mann-Whitney U test was applied. *P < .05, **P < .01, ***P < .001. IP, intraperitoneally.

CiTE leads to eradication of AML cells in a murine NSG xenograft model without indication of enhanced PD-1 upregulation or body weight loss. (A) Experimental design of mouse studies. (B) Remaining engrafted MOLM-13:PD-L1 (live hCD45+CD33+) cells in BM of exemplary mice per cohort (left) and as mean (right) after 13 days. (C) PD-1 upregulation on human CD45+CD3+CD4+ and CD45+CD3+CD4 T cells. (D) Relative body weight of mice as scored during treatment with CiTE and sctb. Cohorts contained 4 to 6 mice. Error bars in (B-C) indicate standard deviation, in (D) SEM. For statistical analysis, Mann-Whitney U test was applied. *P < .05, **P < .01, ***P < .001. IP, intraperitoneally.

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