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. 2013 Dec 16;210(13):2921–2937. doi: 10.1084/jem.20130699

Table 3.

Evaluation of clinical signs and histological EAE in WT, IgHMOG-mem/JHT, and IgHMOG-ki mice

Ag and mice Incidence Onset Mean maximal clinical score Mean number of foci (±SEM)a
Meninges Parenchyma Total
MOG p35–55
WT 15/15 11.5 (±0.4) 3.6 (±0.3) 238 (±53) 203 (±39) 441 (±92)
IgHMOG-mem/JHT 18/18 11.4 (±1.1) 3.7 (±0.3) 117 (±23) 117 (±24) 234 (±47)
IgHMOG-ki 15/15 11.6 (±1.2) 3.8 (±0.2) 118 (±28) 138 (±23) 256 (±51)
rmMOG
WT 15/15 11.3 (±0.6) 3.9 (±0.2) 160 (±33) 199 (±41) 339 (±74)
IgHMOG-mem/JHT 18/18 11.4 (±0.2) 3.9 (±0.2) 189 (±18) 199 (±12) 388 (±30)
IgHMOG-ki 15/15 11.8 (±0.8) 3.8 (±0.3) 137 (±16) 145 (±24) 282 (±30)
rhMOG
WT 18/18 11.8 (±0.5) 3.7 (±0.2) 154 (±47) 150 (±10) 304 (±57)
IgHMOG-mem/JHT 18/18 11.8 (±0.7) 3.0 (±0.2) 118 (±28) 139 (±23) 257 (±51)
IgHMOG-ki 17/18 10.4 (±0.4) 4.2 (±0.3) 146 (±25) 139 (±18) 285 (±43)

Onset indicates mean day of disease onset (paralytic EAE) ± SEM. Clinical score shows mean maximal score of paralytic EAE of diseased mice ± SEM. Composite data from three independent experiments with five to six mice per group are indicated.

a

The infiltration in the brain and spinal cord is quantified as averaged number of meningeal and parenchymal inflammatory foci (>10 clustered inflammatory cells) per CNS tissue section (five mice/group).