Zhe Chen, Wei Zhang, Mert Mestanoglu, Claus Cursiefen, Felix Bock
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Therefore, allogeneic donor corneas from C57BL/6N mice were used and graft survival was monitored weekly for 8 weeks. Finally, hem-and lymphangiogenesis as well as the phenotype of antigen-presenting cells (APCs) in draining lymph nodes (dLNs) and corneas were analyzed by immunohistochemistry and FACS, respectively. Both, Aflibercept and Bevacizumab eye drops supported the regression of both blood and lymphatic vessels. Aflibercept-treated corneas demonstrated decreased APC activation in the dLNs after treatment at day 21. In the high-risk transplantation model, both therapeutics could improve graft survival rates (Aflibercept: 60 %, P = 0.0091; Bevacizumab: 50 %, P = 0.0547) compared to control (10 %). Eight weeks post-transplantation, both treatment arms displayed decreased APC recruitment and an increased expression of Foxp3 on CD4<sup>+</sup>CD25<sup>+</sup> T cells. Our study demonstrates that different topically applied anti-VEGF eye drops effectively reduce pre-existing corneal neovascularization and thereby improve subsequent high-risk corneal transplantation. 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In addition, the immune modulatory effects were assessed. After 14 days of suture-induced, inflammatory corneal NV, sutures were removed. Anti-VEGF eye drops or vehicle controls were applied topically 3 times daily for one week. After 21 days, the regression of blood vessels (BVs) and lymphatic vessels (LVs) was assessed via immunofluorescence staining. In addition, corneal grafting was performed in another set of mice. Therefore, allogeneic donor corneas from C57BL/6N mice were used and graft survival was monitored weekly for 8 weeks. Finally, hem-and lymphangiogenesis as well as the phenotype of antigen-presenting cells (APCs) in draining lymph nodes (dLNs) and corneas were analyzed by immunohistochemistry and FACS, respectively. Both, Aflibercept and Bevacizumab eye drops supported the regression of both blood and lymphatic vessels. Aflibercept-treated corneas demonstrated decreased APC activation in the dLNs after treatment at day 21. 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引用次数: 0
摘要
在高风险小鼠角膜移植模型中,首先评估不同外用血管内皮生长因子(VEGF)阻断治疗,即阿非利塞普和贝伐单抗,在促进病理性角膜新生血管(NV)消退方面的效果,其次研究其对移植物存活的影响。并对其免疫调节作用进行了评价。缝合线诱导的炎症性角膜NV 14天后,缝合线被拆除。抗vegf滴眼液或对照体每日局部应用3次,持续1周。21 d后,采用免疫荧光染色法观察大鼠血管(BVs)和淋巴管(LVs)的消退情况。另外,对另一组小鼠进行角膜移植。因此,使用来自C57BL/6N小鼠的异体供体角膜,每周监测移植物存活,持续8周。最后,分别用免疫组织化学和FACS分析引流淋巴结(dln)和角膜中抗原呈递细胞(APCs)的表型和淋巴管生成情况。阿非利西普和贝伐单抗滴眼液都支持血液和淋巴管的消退。阿非利赛治疗的角膜在治疗后第21天显示dln中APC活性降低。在高危移植模型中,与对照组(10%)相比,两种治疗方法均可提高移植物存活率(Aflibercept: 60%, P = 0.0091; Bevacizumab: 50%, P = 0.0547)。移植后8周,两个治疗组均显示APC募集减少,CD4+CD25+ T细胞Foxp3表达增加。我们的研究表明,不同的局部使用抗vegf滴眼液可以有效地减少预先存在的角膜新生血管,从而改善后续的高风险角膜移植。这种转化方法可能成为改善高危角膜移植患者临床结果的一种有希望的策略。
Promotion of vessel regression by local VEGF-A blockade improves the survival rate of corneal transplants.
To primarily evaluate the efficacy of different topical vascular endothelial growth factor (VEGF) blocking treatments, namely Aflibercept and Bevacizumab, in promoting regression of pathologic corneal neovascularization (NV) and secondarily to investigate their effects on graft survival in a high-risk mouse corneal transplantation model. In addition, the immune modulatory effects were assessed. After 14 days of suture-induced, inflammatory corneal NV, sutures were removed. Anti-VEGF eye drops or vehicle controls were applied topically 3 times daily for one week. After 21 days, the regression of blood vessels (BVs) and lymphatic vessels (LVs) was assessed via immunofluorescence staining. In addition, corneal grafting was performed in another set of mice. Therefore, allogeneic donor corneas from C57BL/6N mice were used and graft survival was monitored weekly for 8 weeks. Finally, hem-and lymphangiogenesis as well as the phenotype of antigen-presenting cells (APCs) in draining lymph nodes (dLNs) and corneas were analyzed by immunohistochemistry and FACS, respectively. Both, Aflibercept and Bevacizumab eye drops supported the regression of both blood and lymphatic vessels. Aflibercept-treated corneas demonstrated decreased APC activation in the dLNs after treatment at day 21. In the high-risk transplantation model, both therapeutics could improve graft survival rates (Aflibercept: 60 %, P = 0.0091; Bevacizumab: 50 %, P = 0.0547) compared to control (10 %). Eight weeks post-transplantation, both treatment arms displayed decreased APC recruitment and an increased expression of Foxp3 on CD4+CD25+ T cells. Our study demonstrates that different topically applied anti-VEGF eye drops effectively reduce pre-existing corneal neovascularization and thereby improve subsequent high-risk corneal transplantation. This translational approach could become a promising strategy to improve the clinical outcome of high risk keratoplasty in patients.
期刊介绍:
The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.