Chronic treatment with
WOBE437 reduced disease severity in EAE
female C57BL/6 mice. (A) Time course of clinical score from day 0
to day 20; onset is represented as day 1 (red line). (B) AUC and (C)
maximal clinical score observed from the time course of clinical score,
from day 0 to day 20. (D) Time course of body weight changes from
day −10 to day 20; onset is represented at day 1 (red line).
Administration of vehicle (DMSO, n = 37) or WOBE437
(10 mg/kg, n = 29) started at the individual day
of onset of each mouse; injections (20 μL) were done intraperitoneally
once per day during 20 days. Data show (A, D) mean ± SEM; (B)
median, percentile 25, percentile 75, minimum and maximum; or (C)
cumulative frequency. (A–D) Data show the summary of four different
cohorts, only mice showing symptoms were included in the study. Statistical
differences were determined using (A, D) multiple t-tests corrected for multiple comparison with the Holm–Sidak
method, (B) Mann–Whitney test, or (C) Chi-square test and Fisher’s
exact test. *, p < 0.05 compared to vehicle group.