Peters Swaantje, Heiduschka Peter, Julien Sylvie, Ziemssen Focke, Fietz Heike, Bartz-Schmidt Karl Ulrich, Schraermeyer Ulrich
University Eye Hospital Tübingen, Tübingen, Germany.
Am J Ophthalmol. 2007 Jun;143(6):995-1002. doi: 10.1016/j.ajo.2007.03.007. Epub 2007 Apr 23.
To examine the ultrastructural effect of intravitreal bevacizumab on primate eyes with particular focus set on the choriocapillaris and to examine the influence of vascular endothelial growth factor (VEGF) inhibition on endothelial cell fenestration.
Animal study.
Four Cynomolgus monkeys received an intravitreal injection of 1.25 mg bevacizumab. The eyes were enucleated and prepared for light and electron microscopy on days one, four, seven, and 14. Control eyes remained untreated. Choriocapillaris endothelial cell fenestrations were quantified.
Choriocapillaris endothelial cell fenestrations were significantly reduced after intravitreal injection of bevacizumab. Fenestration was lowest on day four (15.9 +/- 6.7 per 25 microm) and increased again from days seven to 14, but was still significantly lower than in the control (66.2 +/- 9.5 per 25 microm). Densely packed thrombocytes and leukocytes regionally occluded the choriocapillaris lumen of treated eyes. On day one an increased number of leukocytes filled in the choriocapillaris lumen. Photoreceptors were damaged in two of 40 light microscopic sections. On days one to seven, choroidal melanocytes contained giant melanosomes. None of these described features was found in controls.
Intravitreal bevacizumab causes ultrastructural changes in the choriocapillaris of primate eyes. A significant reduction of choriocapillaris endothelial cell fenestrations is seen as early as 24 hours after injection and their number increases again after two weeks. These findings may play a role in the early clinical effect of intravitreal bevacizumab for macular edema. Because an increased risk of circulation disturbances in the choriocapillaris cannot be excluded, patients should be carefully monitored.
研究玻璃体内注射贝伐单抗对灵长类动物眼睛的超微结构影响,特别关注脉络膜毛细血管,并研究血管内皮生长因子(VEGF)抑制对内皮细胞窗孔的影响。
动物研究。
4只食蟹猴接受玻璃体内注射1.25mg贝伐单抗。在第1、4、7和14天摘除眼球并制备用于光镜和电镜检查的样本。对照眼不做处理。对脉络膜毛细血管内皮细胞窗孔进行定量分析。
玻璃体内注射贝伐单抗后,脉络膜毛细血管内皮细胞窗孔显著减少。第4天时窗孔最少(每25μm为15.9±6.7个),从第7天到第14天又有所增加,但仍显著低于对照组(每25μm为66.2±9.5个)。密集堆积的血小板和白细胞局部阻塞了治疗眼的脉络膜毛细血管腔。第1天时,脉络膜毛细血管腔内白细胞数量增加。40个光镜切片中有2个出现光感受器损伤。在第1至7天,脉络膜黑素细胞含有巨大黑素小体。对照组未发现上述任何特征。
玻璃体内注射贝伐单抗可导致灵长类动物眼睛脉络膜毛细血管发生超微结构改变。注射后24小时内即可观察到脉络膜毛细血管内皮细胞窗孔显著减少,两周后其数量再次增加。这些发现可能在玻璃体内注射贝伐单抗治疗黄斑水肿的早期临床效果中发挥作用。由于不能排除脉络膜毛细血管循环障碍风险增加的可能性,因此应仔细监测患者。