Journal
BRITISH JOURNAL OF OPHTHALMOLOGY
Volume 93, Issue 8, Pages 1075-1080Publisher
BMJ PUBLISHING GROUP
DOI: 10.1136/bjo.2008.145128
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Funding
- German Research Council [Cu 47/1-1, Cu 47/1-2]
- National Eye Institute [EY10765]
- Interdisciplinary Center for Clinical Research (IZKF) Erlangen
- ELAN fund for Science and Teaching Erlangen
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Background: High-risk keratoplasties are usually performed after an uninflamed and quiescent interval in corneas with partly regressed blood and lymphatic vessels. We analysed whether the inhibition of post-keratoplasty revascularisation in mice with partly regressed corneal vessels (intermediate-risk'') improves graft survival. Methods: Three interrupted stromal sutures (11-0) in corneas of Balb/c mice (6-8 weeks old) were placed for 6 weeks. Six months after suture removal, penetrating keratoplasty was performed with C57BL/6 donors. The treatment group received a vascular endothelial growth factor-A specific cytokine trap (VEGF Trap) intraperitoneally at days 0, 4, 7 and 14 after keratoplasty (25 mg/kg per mouse; controls received equal amounts of Fc protein). Pathological haemangiogenesis and lymphangiogenesis prior to as well as 3 days or 8 weeks after keratoplasty and graft survival were analysed. Results: Three days after keratoplasty corneal revascularisation was sufficiently reduced by VEGF Trap (haemvascularised areas 42.7% reduction; lymph-vascularised areas 54.7% reduction). Survival proportions 8 weeks after keratoplasty were 36% in the treatment group compared with 9% in the control group (n = 11; p<0.05). At that time no differences in haemangiogenesis or lymphangiogenesis were observed between the two groups. Conclusion: Early transient postoperative induction of haemangiogenesis and lymphangiogenesis and reformation of regressed corneal blood and lymphatic vessels are important for transplant rejections after intermediaterisk'' corneal transplantation.
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