The immune privilege of corneal allografts

Authors
Citation
Jy. Niederkorn, The immune privilege of corneal allografts, TRANSPLANT, 67(12), 1999, pp. 1503-1508
Citations number
55
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
67
Issue
12
Year of publication
1999
Pages
1503 - 1508
Database
ISI
SICI code
0041-1337(19990627)67:12<1503:TIPOCA>2.0.ZU;2-Y
Abstract
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 .