A neuropathological analysis of experimental autoimmune encephalomyelitis with predominant brain stem and cerebellar involvement and differences between active and passive induction
Dm. Muller et al., A neuropathological analysis of experimental autoimmune encephalomyelitis with predominant brain stem and cerebellar involvement and differences between active and passive induction, ACT NEUROP, 100(2), 2000, pp. 174-182
Experimental autoimmune encephalomyelitis (EAE) is an autoimmune demyelinat
ing disease that can be induced in a variety of animal species and which is
commonly used as an animal model of multiple sclerosis. In rodent EAE mode
ls, the clinical disease is typified by ascending paralysis; however, other
clinical patterns can also be observed by inducing disease with particular
peptides of myelin proteolipid protein (PLP) or myelin oligodendrocyte gly
coprotein. Here we describe EAE induced in C3H/HeJ mice by inoculation with
residues 190-209 of PLP. This form of EAE is manifested clinically by a mo
vement disorder, with axial rotation of the head and trunk. Histologically,
this form of EAE is characterized by predominant cerebellar or brain stem
involvement, depending on whether EAE is induced by active immunization wit
h the PLP peptide, or by passive transfer of T cells specific for the pepti
de. The inflammatory cell infiltrate is composed of polymorphonuclear cells
and mononuclear cells. This rotatory form of EAE may be a useful model for
studying the neuropathological characteristics of multiple sclerosis affec
ting the brain stem and cerebellum.