Skip to main content
. Author manuscript; available in PMC: 2008 Oct 21.
Published in final edited form as: Viral Immunol. 2008 Jun;21(2):173–188. doi: 10.1089/vim.2008.0014

Table 1.

Administration of Anti-IL-23p19 and Anti-IL-12/23p40 Reduces EAE Clinical Disease

Treatment regimen Incidence Median time to onset (days) Disease burden over time (mean ± SEM) Highest acute clinical sign (mean ± SEM) No. of relapses (mean ± SEM) Relapse severity (mean ± SEM)
Day −1 (start)
PBS 13/13 (100%) 22.5 1.66 ± 0.20 3.6 ± 0.3 0.7 ± 0.2 3.8 ± 0.1
Rat IgG 11/11 (100%) 21.5 1.27 ± 0.20 3.8 ± 0.4 0.5 ± 0.2 3.5 ± 0.3
Anti-IL-12/23p40 3/6 (50%)a,b >69a,b 0.18 ± 0.24a,b 0.8 ± 0.5a,b 0.0 ± 0.0 0.0 ± 0.0
Anti-IL-23p19 8/9 (89%) 51.0a,b 0.80 ± 0.24a 2.8 ± 0.5 0.4 ± 0.2 3.3 ± 0.3
a

Significantly different from PBS at p < 0.05.

b

Significantly different from rat IgG at p < 0.05.