Sheffield Institute for Translational Neuroscience (SITraN), Division of Neuroscience, University of Sheffield, Sheffield, UK.
Neuroscience Institute, University of Sheffield, Western Bank, Sheffield, UK.
EMBO Mol Med. 2024 Nov;16(11):2882-2917. doi: 10.1038/s44321-024-00148-5. Epub 2024 Oct 2.
Spastic paraplegia 47 (SPG47) is a neurological disorder caused by mutations in the adaptor protein complex 4 β1 subunit (AP4B1) gene leading to AP-4 complex deficiency. SPG47 is characterised by progressive spastic paraplegia, global developmental delay, intellectual disability and epilepsy. Gene therapy aimed at restoring functional AP4B1 protein levels is a rational therapeutic strategy to ameliorate the disease phenotype. Here we report that a single delivery of adeno-associated virus serotype 9 expressing hAP4B1 (AAV9/hAP4B1) into the cisterna magna leads to widespread gene transfer and restoration of various hallmarks of disease, including AP-4 cargo (ATG9A) mislocalisation, calbindin-positive spheroids in the deep cerebellar nuclei, anatomical brain defects and motor dysfunction, in an SPG47 mouse model. Furthermore, AAV9/hAP4B1-based gene therapy demonstrated a restoration of plasma neurofilament light (NfL) levels of treated mice. Encouraged by these preclinical proof-of-concept data, we conducted IND-enabling studies, including immunogenicity and GLP non-human primate (NHP) toxicology studies. Importantly, NHP safety and biodistribution study revealed no significant adverse events associated with the therapeutic intervention. These findings provide evidence of both therapeutic efficacy and safety, establishing a robust basis for the pursuit of an IND application for clinical trials targeting SPG47 patients.
痉挛性截瘫 47 型(SPG47)是一种由衔接蛋白复合物 4β1 亚基(AP4B1)基因突变引起的神经退行性疾病,导致 AP-4 复合物缺乏。SPG47 的特征是进行性痉挛性截瘫、全面发育迟缓、智力残疾和癫痫。旨在恢复功能性 AP4B1 蛋白水平的基因治疗是改善疾病表型的合理治疗策略。在这里,我们报告单次鞘内注射表达 hAP4B1 的腺相关病毒血清型 9(AAV9/hAP4B1)可导致广泛的基因转移和多种疾病特征的恢复,包括 AP-4 货物(ATG9A)定位错误、小脑深部核中的钙结合蛋白阳性球体、解剖学脑缺陷和运动功能障碍,在 SPG47 小鼠模型中。此外,AAV9/hAP4B1 为基础的基因治疗显示出治疗小鼠血浆神经丝轻链(NfL)水平恢复。基于这些临床前概念验证数据,我们进行了 IND 可行性研究,包括免疫原性和 GLP 非人类灵长类动物(NHP)毒理学研究。重要的是,NHP 安全性和生物分布研究表明,治疗干预没有与任何重大不良事件相关。这些发现提供了治疗效果和安全性的证据,为针对 SPG47 患者的临床试验申请 IND 奠定了坚实的基础。