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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Ciliary neurotrophic factor (CNTF) for human retinal degeneration: Phase I trial of CNTF delivered by encapsulated cell intraocular implants
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Ciliary neurotrophic factor (CNTF) for human retinal degeneration: Phase I trial of CNTF delivered by encapsulated cell intraocular implants

机译:睫状神经营养因子(CNTF)用于人类视网膜变性:包裹细胞眼内植入物递送CNTF的I期试验

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摘要

Neurotrophic factors are agents with a promising ability to retard progression of neurodegenerative diseases and are effective in slowing photoreceptor degeneration in animal models of retinitis pigmentosa. Here we report a human clinical trial of a neurotrophic factor for retinal neurodegeneration. In this Phase I safety trial, human ciliary neurotrophic factor (CNTF) was delivered by cells transfected with the human CNTF gene and sequestered within capsules that were surgically implanted into the vitreous of the eye. The outer membrane of the encapsulated cell implant is semipermeable to allow CNTF to reach the retina. Ten participants received CNTF implants in one eye. When the implants were removed after 6 months, they contained viable cells with minimal cell loss and gave CNTF output at levels previously shown to be therapeutic for retinal degeneration in rcd1 dogs. Although the trial was not powered to form a judgment as to clinical efficacy, of seven eyes for which visual acuity could be tracked by conventional reading charts, three eyes reached and maintained improved acuities of 10-15 letters, equivalent to two- to three-line improvement on standard Snellen acuity charts. A surgically related choroidal detachment in one eye resulted in a transient acuity decrease that resolved with conservative management. This Phase I trial indicated that CNTF is safe for the human retina even with severely compromised photoreceptors. The approach to delivering therapeutic proteins to degenerating retinas using encapsulated cell implants may have application beyond disease caused by genetic mutations.
机译:神经营养因子是具有延缓神经退行性疾病进展的有前途能力的物质,并且在减慢色素性视网膜炎动物模型中有效减缓感光器变性。在这里,我们报告了视网膜神经变性的神经营养因子的人类临床试验。在这一I期安全性试验中,人睫状神经营养因子(CNTF)由被人CNTF基因转染的细胞递送,并被隔离在通过外科手术植入眼玻璃体内的胶囊中。包封的细胞植入物的外膜是半透性的,以允许CNTF到达视网膜。十名参与者用一只眼睛接受了CNTF植入物。 6个月后取下植入物时,它们包含的活细胞具有最小的细胞损失,并且CNTF的输出量达到了先前显示的对rcd1狗视网膜变性的治疗水平。尽管该试验无法对临床疗效做出判断,但可以通过常规阅读表追踪视力的七只眼中,有三只眼达到并保持了10-15个字母的改良视力,相当于两到三只。标准Snellen视力表的直线改进。一只眼睛的外科手术相关脉络膜脱离导致暂时性视力下降,可通过保守治疗解决。这项第一阶段试验表明,即使有严重受损的感光细胞,CNTF对人的视网膜也是安全的。使用封装的细胞植入物将治疗性蛋白质递送至视网膜退化的方法可能具有超越遗传突变引起的疾病的应用。

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