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Murine Corneal Transplantation: a Model to Study the Most Common Form of Solid Organ Transplantation

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Journal J Vis Exp
Date 2014 Dec 10
PMID 25490741
Citations 5
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Abstract

Corneal transplantation is the most common form of organ transplantation in the United States with between 45,000 and 55,000 procedures performed each year. While several animal models exist for this procedure and mice are the species that is most commonly used. The reasons for using mice are the relative cost of using this species, the existence of many genetically defined strains that allow for the study of immune responses, and the existence of an extensive array of reagents that can be used to further define responses in this species. This model has been used to define factors in the cornea that are responsible for the relative immune privilege status of this tissue that enables corneal allografts to survive acute rejection in the absence of immunosuppressive therapy. It has also been used to define those factors that are most important in rejection of such allografts. Consequently, much of what we know concerning mechanisms of both corneal allograft acceptance and rejection are due to studies using a murine model of corneal transplantation. In addition to describing a model for acute corneal allograft rejection, we also present for the first time a model of late-term corneal allograft rejection.

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References
1.
Cunnusamy K, Chen P, Niederkorn J . IL-17A-dependent CD4+CD25+ regulatory T cells promote immune privilege of corneal allografts. J Immunol. 2011; 186(12):6737-45. PMC: 3110606. DOI: 10.4049/jimmunol.1100101. View

2.
Sugar A, Tanner J, Dontchev M, Tennant B, Schultze R, Dunn S . Recipient risk factors for graft failure in the cornea donor study. Ophthalmology. 2009; 116(6):1023-8. PMC: 2740901. DOI: 10.1016/j.ophtha.2008.12.050. View

3.
Medina C, Rowe A, Yun H, Knickelbein J, Lathrop K, Hendricks R . Azithromycin treatment increases survival of high-risk corneal allotransplants. Cornea. 2013; 32(5):658-66. PMC: 3622761. DOI: 10.1097/ICO.0b013e318274a690. View

4.
Tan Y, Cruz-Guilloty F, Medina-Mendez C, Cutrufello N, Martinez R, Urbieta M . Immunological disruption of antiangiogenic signals by recruited allospecific T cells leads to corneal allograft rejection. J Immunol. 2012; 188(12):5962-9. DOI: 10.4049/jimmunol.1103216. View

5.
Patel S . Graft survival and endothelial outcomes in the new era of endothelial keratoplasty. Exp Eye Res. 2011; 95(1):40-7. PMC: 3902807. DOI: 10.1016/j.exer.2011.05.013. View