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补充抗血管内皮生长因子 A 治疗可预防细针透热治疗消退病理性角膜(LYMPH)血管生成后的再血管化。

Supplemental Anti Vegf A-Therapy Prevents Rebound Neovascularisation After Fine Needle Diathermy Treatment to Regress Pathological Corneal (LYMPH)Angiogenesis.

机构信息

Department of Ophthalmology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Köln, Germany.

Department of Ophthalmology, Hue College of Medicine and Pharmacy, Hue University, Hue, Vietnam.

出版信息

Sci Rep. 2020 Mar 3;10(1):3908. doi: 10.1038/s41598-020-60705-z.

Abstract

Fine needle diathermy (FND) is an effective method to destroy and regress pathologic corneal blood and lymphatic vessels. However, it is unknown whether FND itself causes a rebound corneal neovascularisation and whether that can be prevented by VEGF blockade. In female BALB/c mice, the suture-induced inflammatory corneal neovascularisation model was used to induce hem- and lymphangiogenesis. Thereafter, prevascularized mice were divided into 2 groups: the combination therapy group received FND cauterization and subsequent VEGF TrapRR eye drops three times per day whereas the monotherapy group was treated only with FND. Three, 7 and 14 days after the treatment, corneas were collected and stained with FITC-conjugated CD31 and LYVE-1 followed by Cy3-conjugated secondary antibody to quantify corneal blood and lymphatic vessels. Relative mRNA expression of VEGF in the cornea was quantified by using qPCR. FND cauterization as monotherapy significantly obliterated (lymph)angiogenesis at early time points; however, this treatment led to secondary corneal hem- and lymphangiogenesis associated with significant upregulation of pro(lymph)angiogenic VEGF-A, VEGF-C, VEGF-D and infiltration of macrophages. Combining FND cauterization with VEGF TrapRR treatment prevented the undesired effect of the FND procedure alone and significantly better regressed corneal blood and lymphatic vessels at 1 week after the treatment compared to monotherapy and control group (p < 0.01).

摘要

细针透热疗法(FND)是破坏和消退病理性角膜血管和淋巴管的有效方法。然而,尚不清楚 FND 本身是否会引起角膜新生血管的反弹,以及 VEGF 阻断是否可以预防这种反弹。在雌性 BALB/c 小鼠中,使用缝线诱导的炎症性角膜新生血管化模型来诱导血管生成和淋巴管生成。此后,将预血管化的小鼠分为 2 组:联合治疗组接受 FND 电灼治疗,并随后每天滴用 3 次 VEGF TrapRR 滴眼液,而单药治疗组仅接受 FND 治疗。在治疗后 3、7 和 14 天,收集角膜并分别用 FITC 标记的 CD31 和 LYVE-1 染色,然后用 Cy3 标记的二级抗体定量角膜血管和淋巴管。通过 qPCR 定量角膜中 VEGF 的相对 mRNA 表达。作为单药治疗的 FND 电灼显著消除(淋巴管)血管生成在早期时间点;然而,这种治疗导致继发性角膜血管生成和淋巴管生成,与促(淋巴管)血管生成的 VEGF-A、VEGF-C、VEGF-D 的显著上调和巨噬细胞浸润相关。将 FND 电灼与 VEGF TrapRR 联合治疗可预防 FND 程序单独引起的不良影响,并在治疗后 1 周时与单药治疗和对照组相比,显著更好地消退角膜血管和淋巴管(p < 0.01)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c832/7054535/7d3db9646058/41598_2020_60705_Fig1_HTML.jpg

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