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. 2009 Dec;175(6):2430–2438. doi: 10.2353/ajpath.2009.090544

Table 1.

EAE Disease Assessment

Mouse strain* EtOH
PE DHC
P value n
CDI MDD CDI MDD
Wild type 10.1 0.5 19.8 1.0 0.001 28
 TLR2−/− 7.6 0.4 8.3 0.4 0.306 15
 IL-15−/− 9.4 0.5 24.5 1.2 0.001 10
 IL-15Rα−/− 7.0 0.4 18.7 0.9 0.0077 12
Mouse strain Mean incidence
Mean maximum severity
Mean day of onset
EtOH
PE DHC
EtOH
PE DHC
EtOH
PE DHC
Wild type 58.6 75 3.2 3.6 14.4 12.1
 TLR2−/− 42.1 46.6 3.0 2.9 14.4 14.7
 IL-15−/− 60 90 3.1 3.7 14.7 13.0
 IL-15Rα−/− 66 100 2.7 2.9 15.1 13.8
*

The CDI was obtained by summing the daily average disease scores of each experimental group through day 20. A mean of these daily disease scores (MDD) was calculated based on the 20 days of observation. The MDD scores were compared using the Wilcoxon signed rank tests for two samples. n is the total number of mice studied in each experimental group. 

Mean incidence of disease is represented as a percentage and was calculated by dividing the number of mice within each group that developed clinical signs of EAE by the total number of mice in that group. Disease incidence frequencies were compared using χ2 analysis. Mean maximum severity of EAE was calculated for mice that developed EAE by taking the highest score observed for each mouse in the 20-day observation period and averaging these values among mice in the same group. Statistical significance was determined using the Wilcoxon signed rank test. Mean day of onset of EAE was calculated for mice that developed EAE by using the first day of observance of signs of EAE as the value and averaging these values among mice in the same group. Statistical significance was determined using Student’s t-test.