Gene replacement therapy provides benefit in an adult mouse model of Leigh syndrome

被引:27
作者
Reynaud-Dulaurier, Robin [1 ]
Benegiamo, Giorgia [2 ]
Marrocco, Elena [3 ]
Al-Tannir, Racha [1 ]
Surace, Enrico Maria [3 ,4 ]
Auwerx, Johan [2 ]
Decressac, Michael [1 ,3 ]
机构
[1] Univ Grenoble Alpes, Grenoble Inst Neurosci, INSERM, U1216, F-38000 Grenoble, France
[2] Ecole Polytech Fed Lausanne, Lab Integrat & Syst Physiol, Inst Bioengn, CH-1015 Lausanne, Switzerland
[3] Telethon Inst Genet & Med TIGEM, I-80078 Pozzuoli, Italy
[4] Univ Naples Federico II, Med Genet, Dept Translat Med, I-80131 Naples, Italy
基金
欧洲研究理事会; 瑞士国家科学基金会; 新加坡国家研究基金会;
关键词
gene therapy; neurometabolic disease; mitochondria; AAV vector; COMPLEX-I DEFICIENCY; DISEASE; INFLAMMATION; DELIVERY; HYPOXIA; NDUFS4;
D O I
10.1093/brain/awaa105
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mutations in nuclear-encoded mitochondrial genes are responsible for a broad spectrum of disorders among which Leigh syndrome is the most common in infancy. No effective therapies are available for this severe disease mainly because of the limited capabilities of the standard adeno-associated viral (AAV) vectors to transduce both peripheral organs and the CNS when injected systemically in adults. Here, we used the brain-penetrating AAV-PHP.B vector to reinstate gene expression in the Ndufs4 knockout mouse model of Leigh syndrome. Intravenous delivery of an AAV.PHP.B-Ndufs4 vector in 1-month-old knockout mice restored mitochondrial complex I activity in several organs including the CNS. This gene replacement strategy extended lifespan, rescued metabolic parameters, provided behavioural improvement, and corrected the pathological phenotype in the brain, retina, and heart of Ndufs4 knockout mice. These results provide a robust proof that gene therapy strategies targeting multiple organs can rescue fatal neurometabolic disorders with CNS involvement.
引用
收藏
页码:1686 / 1696
页数:11
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