Figure 4
Figure 4. Splenocytes from mice receiving anti–IL-21 mAb have decreased numbers of cells secreting IFN-[gamma], IL-17, and GrB. Spleens were isolated on day 10 and day 20 from NOD/SCID/γc−/− mice receiving human PBMCs (30 × 106 cells) that were treated with nothing, anti–IL-21 mAb, or isotype control antibody, and splenocytes were stimulated with phorbol myristate acetate and ionomycin and assayed using intracellular cytokine staining. Average percentage (± SEM) of cells secreting IFN-γ (A-B), IL-4 (C-D), IL-17 (E-F), and GrB (G-H) on day 10 (A,C,E,G) or day 20 (B,D,F,H). n = 4 mice for each time point (day 10 and day 20) and for each treatment group.

Splenocytes from mice receiving anti–IL-21 mAb have decreased numbers of cells secreting IFN-[gamma], IL-17, and GrB. Spleens were isolated on day 10 and day 20 from NOD/SCID/γc−/− mice receiving human PBMCs (30 × 106 cells) that were treated with nothing, anti–IL-21 mAb, or isotype control antibody, and splenocytes were stimulated with phorbol myristate acetate and ionomycin and assayed using intracellular cytokine staining. Average percentage (± SEM) of cells secreting IFN-γ (A-B), IL-4 (C-D), IL-17 (E-F), and GrB (G-H) on day 10 (A,C,E,G) or day 20 (B,D,F,H). n = 4 mice for each time point (day 10 and day 20) and for each treatment group.

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