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用于人类视网膜变性的睫状神经营养因子(CNTF):通过封装细胞眼内植入物递送CNTF的I期试验。

Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants.

作者信息

Sieving Paul A, Caruso Rafael C, Tao Weng, Coleman Hanna R, Thompson Darby J S, Fullmer Keri R, Bush Ronald A

机构信息

National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3896-901. doi: 10.1073/pnas.0600236103. Epub 2006 Feb 27.

Abstract

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.

摘要

神经营养因子是一类有望延缓神经退行性疾病进展的物质,并且在色素性视网膜炎动物模型中能有效减缓光感受器退化。在此,我们报告一项针对视网膜神经退行性变的神经营养因子人体临床试验。在这项I期安全性试验中,人睫状神经营养因子(CNTF)通过转染了人CNTF基因的细胞递送,并被封装在通过手术植入眼玻璃体的胶囊内。封装细胞植入物的外膜具有半渗透性,以使CNTF能够到达视网膜。10名参与者一只眼睛接受了CNTF植入。6个月后取出植入物时,它们含有存活细胞,细胞损失极少,且CNTF输出水平与先前显示对rcd1犬视网膜变性具有治疗作用的水平相当。尽管该试验未设计用于对临床疗效做出判断,但在7只可通过传统视力表追踪视力的眼睛中,有3只眼睛达到并维持了10 - 15个字母的视力改善,相当于标准斯内伦视力表上提高了两到三行。一只眼睛发生与手术相关的脉络膜脱离,导致视力暂时下降,经保守治疗后恢复。这项I期试验表明,即使在光感受器严重受损的情况下,CNTF对人类视网膜也是安全的。使用封装细胞植入物向退化视网膜递送治疗性蛋白质的方法可能适用于除基因突变引起的疾病之外的其他疾病。

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