RESUMO
In this paper, we described that using wistar rat rather than Lewis rat, an animal model ofexperimental autoimmune encephalomyelitis (EAE) was established. 12 out of 17 rats showedtypical clinical syndroms and pathological changes, and also developed significant delayed-typeskin hypersen-sitivity reaction to the pathogenic antigen-homogenate of guinea pig spinal cord.The cytotoxicity assay demonstrated that the T-cells of EAE rats can specifically lyse the braintissue of normal rats with specific release rate of 15.1l?t 2.79% which is positive correlativewith clinical severity of EAE. The T cell vaccine was prepared by activating EAE T-cells withConA and then treating with glutaraldehyde. Normal rats were inoculated with this T cell vac-cine and challenged with pathogenic antigen one week later. The result showed that all seven ratsgot complete resistance to EAE. T cells from vaccinated animals can specifically lyse the EAE Tcells with specific release rate of 9.38?1.68%.These results indicated: (a)wistar rat can be used for EAE animal model; (b)The incidence ofEAE is associa ted with the auto-reactive T cellsof EAE animals; (c)Inocula tion of this T cellvaccines can prevent the development of EAE, and this protective effect is also mediated by Tcells.