Multiple sclerosis (MS) is a form of chronic encephalomyelitis that re
sults in demyelination of neuronal processes and subsequent neurologic
al dysfunction. Demyelinated plaques are characterised by blood brain
barrier compromise, infiltration of immune cells, and selective loss o
f myelin and oligodendrocyte function. Although there are genetic and
environmental factors, autoimmunity is considered to be central to the
pathogenesis of MS. Experimental allergic/autoimmune encephalomyeliti
s (EAE) is an excellent model of immune-mediated demyelination and has
provided insight into the disease course of MS. Because EAE has a sim
ilar pathophysiology it has also been used as a testing ground for pot
ential therapies of MS. Recent treatment strategies include modulation
of antigen levels, prevention of T cell activation or function, modul
ation of cytokine activity, and promotion of oligodendrocyte regenerat
ion and/or function. This review discusses the current experimental ag
ents that have shown promise in the amelioration of EAE and/or MS.