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在干性年龄相关性黄斑变性非人灵长类动物模型中玻璃体内注射阿伐西普聚乙二醇化产物

Intravitreal Administration of Avacincaptad Pegol in a Nonhuman Primate Model of Dry Age-Related Macular Degeneration.

作者信息

Fujii Rintaro, Matsushita Mayumi, Itani Yoshitaka, Hama Aldric, Natsume Takahiro, Takamatsu Hiroyuki

机构信息

Hamamatsu Pharma Research, Inc., Hamamatsu, Shizuoka, Japan.

出版信息

Pharmacol Res Perspect. 2025 Feb;13(1):e70052. doi: 10.1002/prp2.70052.

Abstract

The lack of effective treatments for dry age-related macular degeneration (AMD) is in part due to a lack of a preclinical animal model that recapitulates features of the clinical state including macular retinal pigment epithelium (RPE) degeneration, also known as geographic atrophy (GA). A nonhuman primate model of GA was developed and its responsiveness to an approved treatment, avacincaptad pegol (ACP), a complement C5 inhibitor, was evaluated. Intravitreal (ivt) administration of sodium iodate (SI) into one eye of male Macaca fascicularis leads to retinal areas (mm) of hyper- or hypo-autofluorescence. Qualitative changes to the retinal structure over time were observed with spectral domain optical coherence tomography (OCT). Six days after SI administration, prior to treatment, mean (± SEM) GA of all eyes was 8.2 ± 1.8 mm. Following randomization to treatment groups, either vehicle or ACP was ivt injected and treatment was continued every 4 weeks, for a total of four treatments. Sixteen weeks after SI administration, the GA area in vehicle-treated eyes was 18.9 ± 6.6 mm, whereas GA in ACP-treated eyes was 11.4 ± 4.0 mm, a reduction by about 36%. Increased, followed by decreased, overall macular thickness was observed with OCT over time following SI administration. Treatment with ACP did not change alter macular thickness thinning. Geographic atrophy-like lesions that expand over time are observed following SI administration. The current macaque model could be utilized to further explore the mechanism of dry AMD and to develop more novel therapeutics.

摘要

干性年龄相关性黄斑变性(AMD)缺乏有效治疗方法,部分原因是缺乏一种能够概括临床状态特征的临床前动物模型,这些特征包括黄斑视网膜色素上皮(RPE)变性,也称为地图样萎缩(GA)。我们开发了一种GA的非人灵长类动物模型,并评估了其对一种已获批治疗药物阿伐西普他德聚乙二醇(ACP,一种补体C5抑制剂)的反应性。向雄性食蟹猴的一只眼睛玻璃体内注射碘酸钠(SI)会导致视网膜区域出现高或低自发荧光(以平方毫米计)。通过光谱域光学相干断层扫描(OCT)观察视网膜结构随时间的定性变化。在注射SI后6天,即在治疗前,所有眼睛的平均(±标准误)GA为8.2±1.8平方毫米。随机分为治疗组后,分别向玻璃体内注射赋形剂或ACP,每4周进行一次治疗,共进行四次治疗。在注射SI后16周,接受赋形剂治疗的眼睛的GA面积为18.9±6.6平方毫米,而接受ACP治疗的眼睛的GA面积为11.4±4.0平方毫米,减少了约36%。在注射SI后,随着时间的推移,OCT观察到黄斑总厚度先增加后减少。ACP治疗并没有改变黄斑厚度变薄的情况。在注射SI后观察到随着时间推移会出现类似地图样萎缩的病变。当前的猕猴模型可用于进一步探索干性AMD的机制,并开发更多新型治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a889/11669843/bf78df462478/PRP2-13-e70052-g001.jpg

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