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通过单次基质内注射腺相关病毒介导的基因疗法预防和治疗神经营养性角膜病变。

Preventing and treating neurotrophic keratopathy by a single intrastromal injection of AAV-mediated gene therapy.

作者信息

Cong Lin, Qi Benxiang, Ma Wenhui, Ren Zhongmei, Liang Qian, Zhou Qingjun, Zhang Bi Ning, Xie Lixin

机构信息

Eye Institute of Shandong First Medical University, Qingdao Eye Hospital of Shandong First Medical University, Qingdao, China; School of Ophthalmology, Shandong First Medical University, Qingdao, China.

Eye Institute of Shandong First Medical University, Qingdao Eye Hospital of Shandong First Medical University, Qingdao, China; School of Ophthalmology, Shandong First Medical University, Qingdao, China; State Key Laboratory Cultivation Base, Shandong Provincial Key Laboratory of Ophthalmology, Qingdao, China.

出版信息

Ocul Surf. 2024 Oct;34:406-414. doi: 10.1016/j.jtos.2024.09.010. Epub 2024 Oct 1.

DOI:10.1016/j.jtos.2024.09.010
PMID:39362525
Abstract

PURPOSE

Neurotrophic keratopathy (NK) is a degenerative corneal condition resulting from corneal nerve injury. Current therapies, including the recombinant human nerve growth factor (rhNGF) therapy, requires continuous administration. This study aims to develop a novel and highly effective gene therapy strategy for the prevention and treatment of NK.

METHODS

Adeno-associated virus (AAV) was transduced into corneal stromal cells by intrastromal injection. Three dimensional corneal wholemount imaging with co-immunostaining of ZO-1 and tubulin was utilized to assess the transduction of AAV.rh10. The efficacy of prevention and treatment of NK by a single intrastromal injection of AAV-Ngf was tested using capsaicin mouse model, herpes simplex keratitis (HSK) model, type Ⅱ diabetes model and alkali burn model. rhNGF eye drops served as the positive control.

RESULTS

Intrastromal injection of AAV.rh10 efficiently transduced the subepithelial nerve plexus and retrogradely transported to the trigeminal ganglion (TG). A single injection of AAV.rh10-Ngf can significantly promote corneal nerve repair, accelerate corneal epithelial repair, reduce corneal stromal edema, and improve corneal sensitivity across the four NK models. The therapeutic effects were consistent with those achieved by continuous administration of rhNGF drops by 6 times daily.

CONCLUSIONS

This proof-of-concept study demonstrates that AAV.rh10-Ngf gene therapy is a promising method for preventing and treating of NK. Our results underline the potential for developing clinical trials to further explore the safety and efficacy of such gene therapy.

摘要

目的

神经营养性角膜病变(NK)是一种由角膜神经损伤导致的角膜退行性疾病。包括重组人神经生长因子(rhNGF)疗法在内的现有治疗方法需要持续给药。本研究旨在开发一种用于预防和治疗NK的新型高效基因治疗策略。

方法

通过基质内注射将腺相关病毒(AAV)转导至角膜基质细胞。利用三维角膜全层成像结合ZO-1和微管蛋白的共免疫染色来评估AAV.rh10的转导情况。使用辣椒素小鼠模型、单纯疱疹性角膜炎(HSK)模型、Ⅱ型糖尿病模型和碱烧伤模型,测试单次基质内注射AAV-Ngf预防和治疗NK的效果。rhNGF滴眼液作为阳性对照。

结果

基质内注射AAV.rh10可有效转导上皮下神经丛并逆行运输至三叉神经节(TG)。单次注射AAV.rh10-Ngf可在四种NK模型中显著促进角膜神经修复、加速角膜上皮修复、减轻角膜基质水肿并提高角膜敏感性。其治疗效果与每日6次持续滴注rhNGF所达到的效果一致。

结论

这项概念验证研究表明,AAV.rh10-Ngf基因治疗是一种有前景的预防和治疗NK的方法。我们的结果突显了开展临床试验以进一步探索这种基因治疗安全性和有效性的潜力。

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