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. 2020 Dec 4;11:588543. doi: 10.3389/fimmu.2020.588543

Figure 5.

Figure 5

ABT 317 reduces the proportion of effector and memory CD8+ T cells in vivo. (A–C): The percentage of KLRG1+ T cells in spleen from 13-week-old NOD mice treated with vehicle or 10 mg/kg ABT 317 for 3 weeks. (A) Representative flow cytometry plot and (B) pooled data from n = 9 individual mice for KLRG1+CD8+ T cells. (C) Pooled data from n = 9 individual mice for KLRG1+CD4+ T cells. (D–F): (D) Representative flow cytometry plots, (E) the percentage of CD44hiCD62LloCD8+ T cells and (F) the percentage of CD44loCD62LhiCD8+ T cells in the spleen from 15–16-week-old NOD mice treated with vehicle or 10 mg/kg ABT 317 for 3 weeks. (G–I): (G) Representative flow cytometry plots, (H) the percentage of CD44hiCD62LloCD4+ T cells and (I) the percentage of CD44loCD62LhiCD4+ T cells in the spleen from 13-week-old NOD mice treated with vehicle or 10 mg/kg ABT 317 for 3 weeks. Pooled data are from n = 9 individual mice with the mean ± SEM. Statistical significance: (B): *P = 0.0234, (C): *P = 0.0140, (E): *P = 0.0156, (F): *P = 0.0106, NS, not significant. Student t test.