We investigated the influence! of an antiparasitic drug, levamisole (2,3,5,
6 - tetrahydro - 6 - phenyl-imidazo (2,1 - b) thiazole hydrochloride) with
potent immunomodulatory properties on the course and development of experim
ental autoimmune encephalomyelitis (EAE). EAE was induced in female Dark Ag
outi (DA) rats aged two months by immunization with guinea pig spinal cord
in complete Freunds adjuvant. Following immunization animals were subcutane
ously treated every other day with 2.2 mg/kg levamisole. The course, develo
pment and characteristics of this autoimmune process were monitored as indi
rect indicators of immune system activity.
Our results indicate that in EAE levamisole exerts immunosuppressive effect
s when administered every other day from the moment of immunization until t
he end of the disease. This application regime and dose postponed the onset
of the first clinical signs, shortened the duration of the disease, abroga
ted the severity of clinical symptoms and accelerated the recovery of sick
animals. In the period of induction and during EAE, levamisole also decreas
ed the severity of changes in the cerebral perivascular spaces. In the peri
pheral blood of levamisole treated animals with induced EAE, a significant
increase of CD4-CD8+ T cells was demonstrated. Furthermore, ail rats with i
nduced EAE had decreased numbers of CD4+CD8- T cells in their blood. These
changes were in correlation with clinical signs of EAE.