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自闭症谱系障碍:基因治疗的治疗前景。

Autism spectrum disorder: prospects for treatment using gene therapy.

机构信息

1Gene Therapy, Centre for Neuroinflammation and Neurodegeneration, Division of Brain Sciences, Faculty of Medicine, Imperial College London, Hammersmith Hospital Campus, W12 0NN, London, UK.

Present address: The Portland Hospital, 205-209 Great Portland Street, London, W1W 5AH UK.

出版信息

Mol Autism. 2018 Jun 20;9:39. doi: 10.1186/s13229-018-0222-8. eCollection 2018.

Abstract

Autism spectrum disorder (ASD) is characterised by the concomitant occurrence of impaired social interaction; restricted, perseverative and stereotypical behaviour; and abnormal communication skills. Recent epidemiological studies have reported a dramatic increase in the prevalence of ASD with as many as 1 in every 59 children being diagnosed with ASD. The fact that ASD appears to be principally genetically driven, and may be reversible postnatally, has raised the exciting possibility of using gene therapy as a disease-modifying treatment. Such therapies have already started to seriously impact on human disease and particularly monogenic disorders (e.g. metachromatic leukodystrophy, SMA type 1). In regard to ASD, technical advances in both our capacity to model the disorder in animals and also our ability to deliver genes to the central nervous system (CNS) have led to the first preclinical studies in monogenic ASD, involving both gene replacement and silencing. Furthermore, our increasing awareness and understanding of common dysregulated pathways in ASD have broadened gene therapy's potential scope to include various polygenic ASDs. As this review highlights, despite a number of outstanding challenges, gene therapy has excellent potential to address cognitive dysfunction in ASD.

摘要

自闭症谱系障碍(ASD)的特征是社交互动受损;受限、固执和刻板的行为;以及异常的沟通技巧。最近的流行病学研究报告称,ASD 的患病率急剧上升,多达每 59 名儿童中就有 1 名被诊断为 ASD。ASD 似乎主要是由遗传驱动的,并且可能在出生后具有逆转性,这就提出了一个令人兴奋的可能性,即使用基因治疗作为疾病修饰治疗。这些治疗方法已经开始对人类疾病产生重大影响,特别是单基因疾病(例如异染性脑白质营养不良、SMA 型 1)。就 ASD 而言,我们在动物模型中模拟该疾病的能力以及向中枢神经系统(CNS)传递基因的能力的技术进步,导致了单基因 ASD 的首次临床前研究,包括基因替换和沉默。此外,我们对 ASD 中常见失调途径的认识和理解不断加深,扩大了基因治疗的潜在范围,包括各种多基因 ASD。正如这篇综述所强调的,尽管存在许多悬而未决的挑战,但基因治疗具有很好的潜力来解决 ASD 的认知功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f554/6011246/82ea8fec1882/13229_2018_222_Fig1_HTML.jpg

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