Background Corneal transplantation is the oldest, most common, and arguably
, the most successful form of tissue transplantation. In the United States
alone, over 40,000 corneal transplantations are performed each year, Less t
han 10% of the uncomplicated, first-time corneal grafts will undergo immune
rejection even though HLA matching is not routinely performed and the use
of immunosuppressive drugs is limited to the topical application of cortico
steroids. The success of corneal transplantations predates the use of corti
costeroids and further emphasizes the remarkable privilege of corneal allog
rafts.
Methods. Several laboratories have used rat and mouse models of orthotopic
corneal transplantation (keratoplasty) in an attempt to understand the basi
s for the immune privilege of corneal allografts.
Results. The time-honored explanation for the immune privilege of corneal a
llografts was based on the conspicuous avascularity of the cornea, which wa
s believed to sequester the graft from the immune apparatus. However, resul
ts from several laboratories indicate that at least three additional featur
es of the corneal graft contribute to its immune privileged status: (a) abs
ence of donor-derived, antigen-presenting passenger Langerhans cells in the
corneal graft; (b) expression of Fas ligand on the epithelium and endothel
ium of the corneal allograft; and (c) capacity of the corneal allograft to
induce immune deviation of the systemic immune response.
Conclusions. The immune privilege of corneal allografts is a product of at
least three unique qualities of the corneal allograft that conspire to inte
rfere with the induction and expression of allodestructive immune responses
.