Nasir Gibran, Chopra Rajiv, Elwood Fiona, Ahmed Seemin S
Department of Neuroscience, Novartis Institutes for BioMedical Research (NIBR), Cambridge, MA, United States.
AllianThera Biopharma, Boston, MA, United States.
Front Med (Lausanne). 2021 Nov 11;8:760236. doi: 10.3389/fmed.2021.760236. eCollection 2021.
Krabbe Disease (KD) is an autosomal metabolic disorder that affects both the central and peripheral nervous systems. It is caused by a functional deficiency of the lysosomal enzyme, galactocerebrosidase (GALC), resulting in an accumulation of the toxic metabolite, psychosine. Psychosine accumulation affects many different cellular pathways, leading to severe demyelination. Although there is currently no effective therapy for Krabbe disease, recent gene therapy-based approaches in animal models have indicated a promising outlook for clinical treatment. This review highlights recent findings in the pathogenesis of Krabbe disease, and evaluates AAV-based gene therapy as a promising strategy for treating this devastating pediatric disease.
克拉伯病(KD)是一种常染色体代谢紊乱疾病,会影响中枢神经系统和周围神经系统。它是由溶酶体酶半乳糖脑苷脂酶(GALC)功能缺陷引起的,导致有毒代谢物精神鞘氨醇积累。精神鞘氨醇的积累会影响许多不同的细胞途径,导致严重的脱髓鞘。虽然目前尚无治疗克拉伯病的有效疗法,但最近在动物模型中基于基因治疗的方法为临床治疗带来了有希望的前景。本综述重点介绍了克拉伯病发病机制的最新研究结果,并评估了基于腺相关病毒(AAV)的基因治疗作为治疗这种毁灭性儿科疾病的一种有前景的策略。