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. 2010 Jun 8;120(2):223–236. doi: 10.1007/s00401-010-0704-z

Table 1.

Characterization of the experimental models and of the MS tissues used

Experimental models/MS tissue Description No. of animals/cases No. of lesions
T-cell EAE T-cell inflammation, macrophage activation, edema 3 per time point 108
T-cell EAE +MOG Ab T-cell inflammation, macrophage activation, blood brain barrier damage, demyelination (antibody + complement deposition) 5 30
T-cell EAE +NMO Ab T-cell inflammation, macrophage activation, blood brain barrier damage, primary astrocytic destruction (antibody + complement deposition) (secondary demyelination) 4 24
Active EAE +NMO Ab As T-cell EAE + NMO antibodies, but protracted active disease and blood brain barrier damage 3 15
LPS Active phase of inflammation (granulocytes, few T cells) followed by microglia activation, macrophage recruitment and demyelination 3 per time point 42
Saline Transient mild acute inflammation (granulocytes) 6 12
MS pattern III Inflammatory demyelination, axonal injury, hypoxia-like tissue injury, mitochondrial damage 6 21
MS pattern II Inflammatory demyelination, axonal injury, deposition of immunoglobulin + activated complement 2 14
Progressive MS (slowly expanding) Moderate inflammation, slowly progressive demyelination, axonal injury, T cells + macrophages/microglia 5 11