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多模态成像检测 3 型新生血管小鼠模型中阿柏西普治疗的体内反应。

Multimodal Imaging to Detect in vivo Responses to Aflibercept Therapy in a Mouse Model of Type 3 Neovascularization.

机构信息

Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Milan, Italy.

Complications of Diabetes Unit, Diabetes Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.

出版信息

Ophthalmologica. 2021;244(3):193-199. doi: 10.1159/000513051. Epub 2020 Nov 16.

DOI:10.1159/000513051
PMID:33197922
Abstract

PURPOSE

The aim of this study was to characterize the response to aflibercept in a mouse model of type 3 neovascularization, the neoretinal vascularization (NRV) 2 mouse line.

METHODS

Twelve NRV2 mice were assigned to one of the following groups: (1) 6 mice were injected with aflibercept 3 µg/g at postnatal day (P) 15 ("aflibercept" group), and (2) the remaining 6 mice did not receive any treatment ("placebo" group). The mice were examined at P30 and P44.

RESULTS

The NRV mice's retinas were characterized by regions of depigmentation that were topographically associated with hyperfluorescent lesions seen on fluorescein angiography (FA) images. On optical coherence tomography images, intraretinal neovascularizations were visualized as hyperreflective lesions mainly localized within the outer plexiform and outer nuclear layers. The average number of intraretinal neovascular lesions visualized on FA at P30 was 5.0 ± 2.2 in the aflibercept group and 20.7 ± 2.4 in the placebo group (p < 0.0001). At P44, the average number of intraretinal lesions was still lower in the aflibercept group, although this difference was not statistically significant (p = 0.088).

CONCLUSION

Aflibercept therapy was effective in inhibiting pathologic angiogenesis in the NRV2 mouse model. However, the successive treatment washout resulted in an increase in the number of lesions.

摘要

目的

本研究旨在对 3 型新生血管化的小鼠模型——视网膜新生血管(NRV)2 小鼠系中,阿柏西普的反应进行特征描述。

方法

将 12 只 NRV2 小鼠分为以下两组:(1)6 只小鼠在出生后第 15 天(P)注射 3µg/g 的阿柏西普(“阿柏西普”组),(2)其余 6 只小鼠未接受任何治疗(“安慰剂”组)。于 P30 和 P44 对小鼠进行检查。

结果

NRV 小鼠的视网膜表现为色素脱失区域,与荧光素血管造影(FA)图像上所见的高荧光病变在地形上相关。在光学相干断层扫描图像上,视网膜内新生血管表现为主要定位于外丛状层和外核层的高反射性病变。FA 于 P30 时,阿柏西普组可见的视网膜内新生血管病变的平均数量为 5.0±2.2,安慰剂组为 20.7±2.4(p<0.0001)。于 P44,尽管差异无统计学意义(p=0.088),但阿柏西普组的视网膜内病变数量仍然较低。

结论

阿柏西普治疗可有效抑制 NRV2 小鼠模型中的病理性血管生成。然而,连续治疗冲洗导致病变数量增加。

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