March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Corneal Xenografts: Carrier for the Boston Keratoprosthesis?
Author Affiliations & Notes
  • Andrea Cruzat
    Cornea / Ophthalmology, Harvard Medical Sch/MEEI, Boston, Massachusetts
  • Anita Shukla
    Cornea / Ophthalmology, Harvard Medical Sch/MEEI, Boston, Massachusetts
  • Eleftherios Paschalis
    Cornea / Ophthalmology, Harvard Medical Sch/MEEI, Boston, Massachusetts
  • Fabiano Cade
    Cornea / Ophthalmology, Harvard Medical Sch/MEEI, Boston, Massachusetts
  • Claes Dohlman
    Cornea / Ophthalmology, Harvard Medical Sch/MEEI, Boston, Massachusetts
  • Footnotes
    Commercial Relationships  Andrea Cruzat, None; Anita Shukla, None; Eleftherios Paschalis, None; Fabiano Cade, None; Claes Dohlman, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 4126. doi:
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      Andrea Cruzat, Anita Shukla, Eleftherios Paschalis, Fabiano Cade, Claes Dohlman; Corneal Xenografts: Carrier for the Boston Keratoprosthesis?. Invest. Ophthalmol. Vis. Sci. 2012;53(14):4126.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To study the use of corneal xenografts from different species as Boston Keratoprosthesis (Kpro) carrier in a rabbit model in order to possibly increase donor tissue availability for the Developing World.

Methods: : Three types of surgeries implanting xenografts into Dutch belted rabbit corneas were performed. 1) To assess tissue response, gamma-radiated porcine corneas, gamma-radiated elasmobranch corneas and fresh porcine control corneas were inserted into rabbit corneal stroma. 2) To assess graft rejection in a standard penetrating keratoplasty model, gamma-radiated porcine corneas, gamma radiated elasmobranch corneas and fresh porcine control corneas were transplanted into rabbit corneas. 3) To assess the xenograft tissue as a Boston Kpro carrier, gamma-radiated porcine corneas were transplanted as Kpro carriers into rabbit corneas and were compared to autologous rabbit cornea as controls.

Results: : Our preliminary data shows: 1) Intrastromal xenografts: at 30 days, all fresh porcine controls showed signs of melting whereas the gamma-radiated porcine and gamma-radiated elasmobranch corneas remained intact without signs of rejection or failure. 2) Penetrating keratoplasties in all corneas showed signs of inflammation, opacification and neovascularization after 30 days. 3) Boston Keratoprosthesis: At 30 days, gamma-radiated porcine keratoprosthesis remained intact without signs of rejection or failure - similar in appearance to autologous graft keratoprosthesis.

Conclusions: : Although corneal tissue is available for use as carrier of Boston Keratoprosthesis in the United States, large parts of the Developing World lack such supply. Gamma-radiated xenografts could be an inexpensive solution for the worldwide need for such corneal tissue. Gamma-radiation seems to reduce the xeno-immunity and risk of rejection. It secures sterility and allows easy storage and shipment. Thus, preliminary results show promise for Gamma-radiated corneal xenografts as carriers for the Boston Keratoprosthesis.

Keywords: keratoprostheses • transplantation • radiation therapy 
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