Department of Pediatrics, Division of Pediatric Blood and Marrow Transplantation & Cellular Therapy, University of Minnesota, Minneapolis, Minnesota, USA.
Department of Pediatrics, Division of Pediatric Cardiology, University of Minnesota, Minneapolis, Minnesota, USA.
Ann Neurol. 2023 Dec;94(6):1182-1186. doi: 10.1002/ana.26786. Epub 2023 Sep 23.
Novel therapies for Hurler syndrome aim to cross the blood-brain barrier (BBB) to target neurodegeneration by degrading glycosaminoglycans (GAG). BBB penetration has been assumed with decreased cerebrospinal fluid (CSF) GAG, yet little is known about CSF GAG without brain-targeting therapies. We compared pre-transplant CSF GAG in patients who were treatment naïve (n = 19) versus receiving standard non-BBB penetrating enzyme replacement therapy (ERT, n = 12). In the ERT versus treatment naïve groups, CSF GAG was significantly lower across all content assayed, raising questions about using CSF GAG decrements to show BBB penetration. Future studies should compare GAG reduction in standard versus novel therapies. ANN NEUROL 2023;94:1182-1186.
新型 Hurler 综合征疗法旨在通过降解糖胺聚糖 (GAG) 穿透血脑屏障 (BBB) 以靶向神经退行性变。尽管人们假设 BBB 穿透性与脑脊液 (CSF) GAG 减少有关,但在没有脑靶向治疗的情况下,对 CSF GAG 知之甚少。我们比较了接受治疗前的 CSF GAG 在未接受治疗的患者(n=19)和接受标准非 BBB 穿透酶替代疗法(ERT,n=12)的患者中的水平。在 ERT 与未治疗的组中,所有检测的 CSF GAG 均明显降低,这引发了关于使用 CSF GAG 减少来显示 BBB 穿透性的问题。未来的研究应比较标准与新型疗法中 GAG 的减少情况。