Figure 7.
GPRC5D+ cells are depleted from MM.1S tumors. (A-B) A repeat MM.1S study was conducted testing 1 dose (10 μg) of JNJ-64407564 and control bispecific antibodies. (A) Tumor and blood samples were analyzed on the day after dosing on days 16 and 19 for tumor-cell number by staining with anti-BCMA antibody (percent remaining human CD45+ and BCMA+ cells on the y-axis; first column) and T-cell activation (percent CD25+ and CD4+ or CD8+ T cells on the y-axis; remaining columns). The BCMA antibody was used as a second plasma-cell marker to avoid using a GPRC5D antibody in the ex vivo testing. (B) T-cell (CD3+, CD4+, CD8+; SP57, Ventana) infiltration within the tumors. For each section, the left panel is low magnification (1.5×) and the right panel is a higher magnification (10×).

GPRC5D+ cells are depleted from MM.1S tumors. (A-B) A repeat MM.1S study was conducted testing 1 dose (10 μg) of JNJ-64407564 and control bispecific antibodies. (A) Tumor and blood samples were analyzed on the day after dosing on days 16 and 19 for tumor-cell number by staining with anti-BCMA antibody (percent remaining human CD45+ and BCMA+ cells on the y-axis; first column) and T-cell activation (percent CD25+ and CD4+ or CD8+ T cells on the y-axis; remaining columns). The BCMA antibody was used as a second plasma-cell marker to avoid using a GPRC5D antibody in the ex vivo testing. (B) T-cell (CD3+, CD4+, CD8+; SP57, Ventana) infiltration within the tumors. For each section, the left panel is low magnification (1.5×) and the right panel is a higher magnification (10×).

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