Figure 6.
Lacutamab specifically eliminates KIR3DL2-positive primary ATL cells in an autologous ADCC assay. CD4+ T cells from patients with KIR3DL2-positive ATL (n = 4) or patients with KIR3DL2-negative ATL (n = 4) were preincubated with alemtuzumab (triangles, positive control), isotype control (circles, negative control), or the anti-KIR3DL2 mAb lacutamab (red diamonds). After the addition of autologous NK cells at the indicated E/T ratio, the death of KIR3DL2+ (A) and KIR3DL2− (B) CD4+ tumor cells, and NK cells (C) of patients with KIR3DL2+ ATL was monitored using 7-AAD cell viability stain. As control, the death of KIR3DL2− tumor cells in patients with KIR3DL2− ATL were also assessed (D). The results are expressed as the proportion of cell viability in each cellular population at a given E/T ratio. The cellular populations that were assessed are indicated above each plot. ***P < .001, ns, not significant (two-way ANOVA followed by Sidak’s post-test).

Lacutamab specifically eliminates KIR3DL2-positive primary ATL cells in an autologous ADCC assay. CD4+ T cells from patients with KIR3DL2-positive ATL (n = 4) or patients with KIR3DL2-negative ATL (n = 4) were preincubated with alemtuzumab (triangles, positive control), isotype control (circles, negative control), or the anti-KIR3DL2 mAb lacutamab (red diamonds). After the addition of autologous NK cells at the indicated E/T ratio, the death of KIR3DL2+ (A) and KIR3DL2 (B) CD4+ tumor cells, and NK cells (C) of patients with KIR3DL2+ ATL was monitored using 7-AAD cell viability stain. As control, the death of KIR3DL2 tumor cells in patients with KIR3DL2 ATL were also assessed (D). The results are expressed as the proportion of cell viability in each cellular population at a given E/T ratio. The cellular populations that were assessed are indicated above each plot. ***P < .001, ns, not significant (two-way ANOVA followed by Sidak’s post-test).

Close Modal

or Create an Account

Close Modal
Close Modal