Purpose. Herpes simplex virus type 1 infection of the cornea induces an imm
une-mediated disease termed "herpes stromal keratitis" (HSK) that is a majo
r cause of blindness. In this study we investigated the influence of macrop
hage depletion by CI,MDP encapsulated in liposomes (Cl2MDP-LIP) on the cour
se of HSV-1 keratitis.
Methods. The corneas of BALB/c mice were infected with 10(5) PFU of HSV-1 (
KOS strain). Mice groups received subconjunctival PBS or Cl2MDP-LIP injecti
ons 7 anti 2 days prior to infection. The eyes were studied clinically, his
tologically and immunohistochemically with F4/80 antibody at various time p
oints after treatment. Clearance of the virus from the HSV-infected eyes wa
s measured with a standard plaque assay.
Results. After subconjunctival Cl2MDP-LIP treatment, the HSV-1-induced epit
helial keratitis was more severe (P < 0.05). The virus titers were signific
antly higher after macrophage depletion (day 7, P < 0.005). Stromal keratit
is developed in 78.6% of HSV-1 infected PBS treated control mice (n = 14) b
y day 14 after infection. By subconjunctival Cl2MDP-LIP treatment (n = 14)
the incidence of stromal keratitis was reduced to 42.9%, and the keratitis
was less severe (P < 0.05).
Conclusions. The data demonstrate an influence of macrophages on the course
of HSV-1 keratitis in mice. Macrophage depletion influence the viral repli
cation in the cornea and the immune-mediated process of HSK.