Cs. Constantinescu et E. Lavi, Anterior uveitis in murine relapsing experimental autoimmune encephalomyelitis (EAE), a mouse model of multiple sclerosis (MS), CURR EYE R, 20(1), 2000, pp. 71-76
Purpose. To investigate whether anterior uveitis (AU), which often accompan
ies central nervous system (CNS) and systemic inflammatory diseases includi
ng multiple sclerosis (MS), also develops in a murine relapsing model of MS
, experimental autoimmune encephalomyelitis (EAE) closely resembling relaps
ing-remitting MS, induced by immunization with myelin basic protein (MBP) i
n mice.
Methods. (PL/J x SJL) F1 female mice were immunized with MBP in complete Fr
eund's adjuvant (CFA) using Pertussis toxin as co-adjuvant. EAE was scored
clinically on a scale of 0-5 based on the degree of paralysis. Uveitis was
assessed by slit-lamp biomicroscopy. Histolological analysis of the CNS and
eye were performed.
Results. All immunized mice developed a characteristic relapsing paralysis.
Evidence of AU was present late in the course of EAE, only after the resol
ution of the first clinical relapse, in 4 of 5 mice (80%) (clinical evidenc
e) and 5 of 5 (100%) (histological evidence). AU was mild to moderate with
the exception of one animal, in which it was seven. Involvement was invaria
bly bilateral. Histology showed mononuclear inflitrates in the iris and cil
iary body. Bilateral secondary cataracts were observed in the animal with s
evere inflammation. Paralytic episodes and the AU did not coincide. There w
ere no clinical or histological eye abnormalities in control mice, either n
on-immunized or immunized with CFA and Pertussis toxin only.
Conclusion. We report AU in a mouse model of EAE which strongly resembles r
elapsing MS. These results further suggest shared antigenic determinants be
tween the CNS and the eye, which likely become exposed to the immune system
late in the course of CNS inflammation.