Bascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
Department of Ophthalmology, College of Medicine, University of Florida, Gainesville.
JAMA Ophthalmol. 2014 Apr 1;132(4):409-20. doi: 10.1001/jamaophthalmol.2013.7630.
IMPORTANCE We developed a novel strategy for treatment of Leber hereditary optic neuropathy (LHON) caused by a mutation in the nicotinamide adenine dinucleotide dehydrogenase subunit IV (ND4) mitochondrial gene. OBJECTIVE To demonstrate the safety and effects of the gene therapy vector to be used in a proposed gene therapy clinical trial. DESIGN AND SETTING In a series of laboratory experiments, we modified the mitochondrial ND4 subunit of complex I in the nuclear genetic code for import into mitochondria. The protein was targeted into the organelle by agency of a targeting sequence (allotopic expression). The gene was packaged into adeno-associated viral vectors and then vitreally injected into rodent, nonhuman primate, and ex vivo human eyes that underwent testing for expression and integration by immunohistochemical analysis and blue native polyacrylamide gel electrophoresis. During serial follow-up, the animal eyes underwent fundus photography, optical coherence tomography, and multifocal or pattern electroretinography. We tested for rescue of visual loss in rodent eyes also injected with a mutant G11778A ND4 homologue responsible for most cases of LHON. EXPOSURE Ocular infection with recombinant adeno-associated viral vectors containing a wild-type allotopic human ND4 gene. MAIN OUTCOMES AND MEASURES Expression of human ND4 and rescue of optic neuropathy induced by mutant human ND4. RESULTS We found human ND4 expressed in almost all mouse retinal ganglion cells by 1 week after injection and ND4 integrated into the mouse complex I. In rodent eyes also injected with a mutant allotopic ND4, wild-type allotopic ND4 prevented defective adenosine triphosphate synthesis, suppressed visual loss, reduced apoptosis of retinal ganglion cells, and prevented demise of axons in the optic nerve. Injection of ND4 in the ex vivo human eye resulted in expression in most retinal ganglion cells. Primates undergoing vitreal injection with the ND4 test article and followed up for 3 months had no serious adverse reactions. CONCLUSIONS AND RELEVANCE Expression of our allotopic ND4 vector in the ex vivo human eye, safety of the test article, rescue of the LHON mouse model, and the severe irreversible loss of visual function in LHON support clinical testing with mutated G11778A mitochondrial DNA in our patients.
我们开发了一种治疗莱伯遗传性视神经病变(LHON)的新策略,该病变由线粒体基因 NADH 脱氢酶亚单位 IV(ND4)突变引起。
证明拟议基因治疗临床试验中使用的基因治疗载体的安全性和效果。
在一系列实验室实验中,我们修改了核遗传密码中复合物 I 的线粒体 ND4 亚单位,以使其进入线粒体。该蛋白通过靶向序列(异位表达)靶向细胞器。该基因被包装到腺相关病毒载体中,然后通过玻璃体内注射到啮齿动物、非人灵长类动物和经过测试的离体人眼中,通过免疫组织化学分析和蓝色天然聚丙烯酰胺凝胶电泳检测表达和整合。在连续随访期间,动物眼接受眼底摄影、光学相干断层扫描和多焦点或图形视网膜电图检查。我们还测试了注射突变 G11778A ND4 同源物的啮齿动物眼的视觉丧失挽救情况,该同源物负责大多数 LHON 病例。
重组腺相关病毒载体感染,包含野生型异位人 ND4 基因。
人 ND4 的表达和由突变人 ND4 引起的视神经病变的挽救。
我们发现,注射后 1 周,人 ND4 在几乎所有的老鼠视网膜神经节细胞中表达,并且 ND4 整合到老鼠复合物 I 中。在注射突变异位 ND4 的啮齿动物眼中,野生型异位 ND4 阻止了缺陷型三磷酸腺苷合成,抑制了视觉丧失,减少了视网膜神经节细胞的凋亡,并防止了视神经轴突的死亡。在离体人眼中注射 ND4 导致大多数视网膜神经节细胞表达。接受 ND4 测试物玻璃体内注射并随访 3 个月的灵长类动物没有严重的不良反应。
我们的异位 ND4 载体在离体人眼中的表达、测试品的安全性、LHON 小鼠模型的挽救以及 LHON 中严重不可逆转的视觉功能丧失,支持在我们的患者中用突变的 G11778A 线粒体 DNA 进行临床测试。