Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, 48105, USA.
IMRA America Inc., 1044 Woodridge Ave., Ann Arbor, MI, 48105, USA.
Exp Eye Res. 2022 Oct;223:109215. doi: 10.1016/j.exer.2022.109215. Epub 2022 Aug 13.
Choroidal neovascularization (CNV) in young rabbits has been shown to have a rapid, robust response after treatment with bevacizumab, an anti-vascular endothelial growth factor (VEGF) medication. This investigation evaluates an age differential response to bevacizumab in older populations of rabbits using multimodal high resolution molecular imaging. Young (4 months old) and life span (14 months old) rabbits were given subretinal injections of Matrigel and VEGF to produce CNV. All CNV rabbit models were then treated with a bevacizumab intravitreal injection. Rabbits were then monitored longitudinally using photoacoustic microscopy (PAM), optical coherence tomography (OCT), color photography, and fluorescence imaging. Chain-like gold nanoparticle clusters (CGNP) conjugated with tripeptide arginylglycylaspartic acid (RGD) was injected intravenously for molecular imaging. Robust CNV developed in both young and old rabbits. After intravitreal bevacizumab injection, fluorescence signals were markedly decreased 90.13% in the young group. In contrast, old rabbit CNV area decreased by only 10.56% post-bevacizumab treatment. OCT images confirmed a rapid decrease of CNV in the young group. CGNPs demonstrated high PAM signal in old rabbits and minimal PAM signal in young rabbits after bevacizumab, indicating CNV regression. There is a significant difference in response to intravitreal bevacizumab treatment between young and old rabbits with CNV which can be monitored with multimodal molecular imaging. Old rabbits demonstrate significant persistent disease activity. This represents the first large eye model of persistent disease activity of CNV and could serve as the foundation for future investigations into the mechanism of persistent disease activity and the development of novel therapies.
脉络膜新生血管(CNV)在接受抗血管内皮生长因子(VEGF)药物贝伐单抗治疗后,年轻兔子的反应迅速且强烈。本研究使用多模态高分辨率分子成像技术评估了老年兔子对贝伐单抗的年龄差异反应。将年轻(4 个月大)和寿命(14 个月大)的兔子进行视网膜下注射 Matrigel 和 VEGF 以产生 CNV。所有 CNV 兔模型均接受贝伐单抗玻璃体内注射治疗。然后,使用光声显微镜(PAM)、光学相干断层扫描(OCT)、彩色摄影和荧光成像对兔子进行纵向监测。将三肽精氨酸-甘氨酸-天冬氨酸(RGD)缀合的链状金纳米颗粒簇(CGNP)静脉内注射进行分子成像。年轻和老年兔子均迅速形成明显的 CNV。玻璃体内注射贝伐单抗后,年轻组的荧光信号显著降低了 90.13%。相比之下,老年兔 CNV 面积在贝伐单抗治疗后仅减少了 10.56%。OCT 图像证实了年轻组 CNV 的迅速减少。CGNPs 在老年兔子中显示出较高的 PAM 信号,而在接受贝伐单抗治疗后的年轻兔子中则显示出最小的 PAM 信号,表明 CNV 消退。有脉络膜新生血管的年轻和老年兔子对玻璃体内贝伐单抗治疗的反应存在显著差异,可通过多模态分子成像进行监测。老年兔子表现出明显的持续性疾病活动。这代表了第一个具有持续性疾病活动的 CNV 的大型眼部模型,可为未来研究持续性疾病活动的机制和开发新型疗法奠定基础。