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. 2020 Feb 3;177(5):1061–1076. doi: 10.1111/bph.14897

Figure 4.

Figure 4

Ki‐67 expression on CCR6+/−CD20+ B cells following KLH administration in animals treated with vehicle or i.v. 300 mg·kg−1 VIB4920 in Study 2 (N = 12). VIB4920 treatment inhibits the B‐cell proliferative response following secondary KLH administration. (a) Flow cytometry plots are pre‐gated on CD20+ lymphocytes and show the percent CCR6+/Ki‐67+ for six representative animals; the change over time in circulating (b) CCR6+ (c) CCR6− Ki‑67+ B‐cell count (as frequency of gated CD20+) in animals treated with vehicle, or i.v. 50, 150, or 300 mg·kg−1 VIB4920. Proliferation is significantly affected on Days 15 and 29 of the dosing phase and on Day 43 of the recovery phase. *P ≤ .05, significantly different from vehicle group; one‐way ANOVA with Dunnetts multiple comparisons test with a single pooled variance and the Mann–Whitney test to assess differences in mean rank. CD, cluster of differentiation; i.v., intravenous; KLH, keyhole limpet haemocyanin