Share this article on:

Abstract 16: A Preclinical Swine Model for Whole Eyeball Transplantation Planning and Procedural Aspects

Plastic and Reconstructive Surgery – Global Open: April 2016 - Volume 4 - Issue 4S - p 42
doi: 10.1097/01.GOX.0000488948.07376.ab
PRS PSRC Podium Proofs 2016

This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.

Vasil E. Erbas, MD,* Huseyin Sahin, MD,* Sinan Oksuz, MD,† Liwei Dong, MD,* Maxine R. Miller, MD,* Golnar Shojaati, MD,* Gadi Wollstein, MD,* Kevin C. Chan, PhD,* Ian Sigal, PhD,* Nataliya Kostereva, PhD,* Shailesh Raval, PhD,* Tamer Ibrahim, PhD,* Jeffrey L. Goldberg, MD,‡ Larry Benowitz, MD,§ Joel S. Schuman, MD,* Fatih Zor, MD,¶ Mario Solari, MD,* Kia M. Washington, MD,* Vijay S. Gorantla, MD, PhD*

From the *University of Pittsburgh, Pittsburgh, Pa.; †Gulhane Askeri Tip Akademisi, Ankara, Turkey; ‡Stanford University School of Medicine, Palo Alto, Calif.; §Harvard Medical School, Boston, Mass.; and ¶Gulhane Askeri Tip Akademisi, Istanbul, Turkey.

PURPOSE: Whole eyeball transplantation (WET) is the holy grail of vision restoration and is conceptually the most challenging of vascularized composite allografts. The swine eye is analogous to the human eye and is the ideal model for human WET. Our goal was to develop the protocols (surgical planning/procedures/post operative imaging/evaluations) as a foundation for a robust, large animal, preclinical WET model.

METHODS: WET techniques were optimized in 17 fresh tissue swine dissections. An eyeball-periorbital vascularized composite allograft subunit with extraocular muscles, and optic nerve (ON) was raised superolaterally and anastomosed to the recipient external ophthalmic artery after exenteration. Methylene blue perfusion and microfil vascular mapping of central retinal artery/vortex veins/ciliary plexus was done. Orbital contents and ON were imaged with DCE-DTI-magnetic resonance imaging (T1/T2 MRI at 3T/7T/9.4 Tesla). Advanced protocols for histopathology, immunohistochemistry, epoxy embedding, corrosion casting, and optical coherence tomography/tonometry/fundoscopy/ERG were optimized, and surgical techniques for ON crush, cut, and coaptation were established.

RESULTS: Like humans, the swine retina is holangiotic, and the ON has a lamina cribrosa. However, the central retinal artery is absent with a large external ophthalmic artery. Optical coherence tomography/MRI allowed real-time, high definition, noninvasive, in situ, micron-scale, cross-sectional visualization of structure/topography of ocular structures.

CONCLUSIONS: Our study is the critical first step toward a swine WET model optimized for viability, retinal survival, ON regeneration, and reintegration while documenting key immune responses and enabling key neuroimmunotherapeutic interventions.

© 2016 American Society of Plastic Surgeons