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A new model of corneal transplantation in the miniature pig: efficacy of immunosuppressive treatment
Tavandzi U, Procházka R, Usvald D, Hlucílová J, Vitásková M, Motlík J, Vítová A, Filipec M, Forrester JV, Holán V.
Language English Country United States
Grant support
NR8340
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Journals@Ovid Ovid Full Text
from 2000-01-01 to 2010-02-01
- MeSH
- Financing, Organized MeSH
- Immunosuppressive Agents therapeutic use MeSH
- Drug Therapy, Combination MeSH
- Swine, Miniature MeSH
- Models, Animal MeSH
- Swine MeSH
- Graft Survival drug effects MeSH
- Graft Rejection prevention & control MeSH
- Corneal Transplantation immunology methods MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
Corneal allograft rejection is frequently studied in small rodent or rabbit models. To study mechanisms of rejection in a model that more closely mimics transplantation in humans, we performed orthotopic corneal transplantation in the miniature pig using a 7-mm diameter donor graft. Four groups of recipients were studied: 1) untreated naive, 2) untreated vascularized (high risk), 3) high-risk grafts treated by topical application of prednisolone, or 4) high-risk grafts treated with a combined systemic immunosuppression regime of oral prednisone, cyclosporine A, and mycophenolate mofetil. Both the clinical features and histological assessment of corneal graft rejection showed close similarities to graft rejection in humans. Interestingly, preliminary results indicated that topical steroid treatment was superior to systemic immunosuppression in significantly promoting graft survival. Thus, corneal transplantation in the pig represents an animal model most closely resembling corneal grafting in humans, and offers possibilities for testing various clinically applicable immunosuppressive treatments.
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- $a Corneal allograft rejection is frequently studied in small rodent or rabbit models. To study mechanisms of rejection in a model that more closely mimics transplantation in humans, we performed orthotopic corneal transplantation in the miniature pig using a 7-mm diameter donor graft. Four groups of recipients were studied: 1) untreated naive, 2) untreated vascularized (high risk), 3) high-risk grafts treated by topical application of prednisolone, or 4) high-risk grafts treated with a combined systemic immunosuppression regime of oral prednisone, cyclosporine A, and mycophenolate mofetil. Both the clinical features and histological assessment of corneal graft rejection showed close similarities to graft rejection in humans. Interestingly, preliminary results indicated that topical steroid treatment was superior to systemic immunosuppression in significantly promoting graft survival. Thus, corneal transplantation in the pig represents an animal model most closely resembling corneal grafting in humans, and offers possibilities for testing various clinically applicable immunosuppressive treatments.
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