PURPOSE. Endotoxin-induced uveitis (EIU) in rats and mice peaks 24 hours af
ter endotoxin injection and is commonly assumed to be a monophasic disease.
This study examined intraocular inflammation at later time points to deter
mine whether endotoxin injection can induce recurrent intraocular inflammat
ion in strains of mice with high or moderate levels of susceptibility to EI
U.
METHODS. EIU was elicited in two mouse strains with high (C3H/HeN) and mode
rate (FVB/N) susceptibility, by means of intraperitoneal injections of Salm
onella typhimurium endotoxin. Mammatory cells in the anterior and posterior
segments of the eye were counted by a masked observer on histologic sectio
ns of eyes from 1 to 17 days after endotoxin injection.
RESULTS. A bimodal distribution of inflammatory cell infiltration was noted
in eyes from C3H/HeN mice. As previously reported, inflammation peaked at
24 hours after endotoxin injection. However a second, more pronounced peak
of intraocular inflammation occurred approximately 5 days after endotoxin i
njection. FVB/N mice had a single peak of intraocular inflammation 4 days a
fter injection.
CONCLUSIONS. Endotoxin injection in C3H/HeN elicits recurrent intraocular i
nflammation. The previously unrecognized second peak of inflammation is mor
e severe than the initial inflammatory disease. Studies on this second infl
ammatory peak may be useful in determining the pathogenesis of recurrent uv
eitis in humans.