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黏多糖贮积症的酶替代治疗:过去、现在和未来。

Enzyme replacement therapy for mucopolysaccharidoses; past, present, and future.

机构信息

Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA.

Department of Medical and Molecular Sciences, University of Delaware, Newark, DE, USA.

出版信息

J Hum Genet. 2019 Nov;64(11):1153-1171. doi: 10.1038/s10038-019-0662-9. Epub 2019 Aug 27.

DOI:10.1038/s10038-019-0662-9
PMID:31455839
Abstract

Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders, which lack an enzyme corresponding to the specific type of MPS. Enzyme replacement therapy (ERT) has been the standard therapeutic option for some types of MPS because of the ability to start immediate treatment with feasibility and safety and to improve prognosis. There are several disadvantages for current ERT, such as limited impact to the brain and avascular cartilage, weekly or biweekly infusions lasting 4-5 h, the immune response against the infused enzyme, a short half-life, and the high cost. Clinical studies of ERT have shown limited efficacy in preventing or resolving progression in neurological, cardiovascular, and skeletal diseases. One focus is to penetrate the avascular cartilage area to at least stabilize, if not reverse, musculoskeletal diseases. Although early intervention in some types of MPS has shown improvements in the severity of skeletal dysplasia and stunted growth, this limits the desired effect of ameliorating musculoskeletal disease progression to young MPS patients. Novel ERT strategies are under development to reach the brain: (1) utilizing a fusion protein with monoclonal antibody to target a receptor on the BBB, (2) using a protein complex from plant lectin, glycan, or insulin-like growth factor 2, and (3) direct infusion across the BBB. As for MPS IVA and VI, bone-targeting ERT will be an alternative to improve therapeutic efficacy in bone and cartilage. This review summarizes the effect and limitations on current ERT for MPS and describes the new technology to overcome the obstacles of conventional ERT.

摘要

黏多糖贮积症(MPS)是一组溶酶体贮积症,缺乏与特定类型 MPS 相对应的酶。由于具有可行性和安全性,可以立即开始治疗,并改善预后,因此酶替代疗法(ERT)一直是某些类型 MPS 的标准治疗选择。然而,目前的 ERT 存在几个缺点,例如对大脑和无血管软骨的影响有限、每周或每两周输注一次,持续 4-5 小时、对输注酶的免疫反应、半衰期短以及成本高。ERT 的临床研究表明,其在预防或解决神经、心血管和骨骼疾病进展方面的疗效有限。一个重点是穿透无血管软骨区域,至少稳定,如果不能逆转,骨骼肌肉疾病。虽然某些类型的 MPS 的早期干预已经显示出在骨骼发育不良和生长迟缓的严重程度方面的改善,但这限制了改善骨骼疾病进展的预期效果,使其仅适用于年轻的 MPS 患者。正在开发新的 ERT 策略以到达大脑:(1)利用与单克隆抗体融合的蛋白质来靶向 BBB 上的受体,(2)使用来自植物凝集素、糖或胰岛素样生长因子 2 的蛋白质复合物,和(3)直接穿过 BBB 输注。对于 MPS IVA 和 VI,骨靶向 ERT 将是改善骨骼和软骨治疗效果的一种替代方法。本文综述了目前 MPS 的 ERT 的效果和局限性,并描述了克服传统 ERT 障碍的新技术。

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Newborn Screening for Lysosomal Storage Diseases: Methodologies, Screen Positive Rates, Normalization of Datasets, Second-Tier Tests, and Post-Analysis Tools.
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