非人类灵长类干性年龄相关性黄斑变性模型玻璃体内注射无活性Pegol。

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacology Research & Perspectives Pub Date : 2025-02-01 DOI:10.1002/prp2.70052
Rintaro Fujii, Mayumi Matsushita, Yoshitaka Itani, Aldric Hama, Takahiro Natsume, Hiroyuki Takamatsu
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引用次数: 0

摘要

干性年龄相关性黄斑变性(AMD)缺乏有效的治疗方法,部分原因是由于缺乏临床前动物模型来概括临床状态的特征,包括黄斑视网膜色素上皮(RPE)变性,也称为地理萎缩(GA)。建立了GA的非人灵长类动物模型,并评估了其对补体C5抑制剂avacincaptad pegol (ACP)的反应性。将碘酸钠(SI)通过玻璃体内(ivt)注入雄性束状猕猴(Macaca fascularis)的一只眼睛,导致视网膜区域(mm2)出现高或低自身荧光。用光谱域光学相干断层扫描(OCT)观察视网膜结构随时间的质的变化。注射SI后第6天,治疗前全眼平均(±SEM) GA为8.2±1.8 mm2。随机分配到治疗组后,每4周注射一次载体或ACP,持续治疗,共4次治疗。SI给药16周后,载具组的GA面积为18.9±6.6 mm2,而acp组的GA面积为11.4±4.0 mm2,减少了约36%。在注射SI后的一段时间内,用OCT观察到整体黄斑厚度先增加后减少。ACP治疗未改变黄斑厚度变薄。注射SI后可观察到随时间扩大的地理萎缩样病变。目前的猕猴模型可用于进一步探索干性AMD的发病机制和开发更多新的治疗方法。
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Intravitreal Administration of Avacincaptad Pegol in a Nonhuman Primate Model of Dry Age-Related Macular Degeneration.

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 (mm2) 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 mm2. 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 mm2, whereas GA in ACP-treated eyes was 11.4 ± 4.0 mm2, 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.

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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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