Leukocyte trafficking from blood into tissue is a fundamental process
in immune surveillance and the immune response to stimuli. Experimenta
l autoimmune uveitis (EAU) is an animal model for posterior uveitis an
d is mediated by T lymphocytes and macrophages that infiltrate the pos
terior segment of the eye. To analyze leukocyte migration into retinal
tissue during the course of EAU, labeled cells were identified in viv
o by scanning laser ophthalmoscopy and hi retinal flatmounts by confoc
al microscopy. Adhesion of blood leukocytes to retinal endothelial cel
ls in vivo was significantly raised 48 h before the appearance of clin
ical disease, and this correlated with the in creased expression of CD
54 on retinal vessels. Mitogen-activated spleen cells and CD4(+) T cel
ls only entered into retinal tissue in animals with clinical disease a
nd not naive recipients. The disease status of the donor animal had no
effect on leukocyte trafficking. These results, which identify leukoc
yte-endothelial cell interactions in vivo, suggest that the activation
of the retinal endothelium is a prerequisite to leukocyte adhesion an
d extravasation into ocular tissue during EAU.