Dickson P I
Division of Medical Genetics, Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA 90502, USA.
Int J Clin Pharmacol Ther. 2009;47 Suppl 1:S124-7.
Intrathecal enzyme replacement therapy (ERT) holds promise as a treatment for the central nervous system manifestations of lysosomal storage diseases. Treatment via the cerebrospinal fluid represents a potential method of delivering recombinant enzyme across the blood-brain barrier. Experiments in animal models of mucopolysaccharidosis (MPS) Type I, MPS II and MPS IIIA have shown that ERT delivered via the intrathecal route distributes throughout the central nervous system and penetrates brain tissue, where it promotes clearance of lysosomal storage material. Studies are underway to investigate the safety and efficacy of intrathecal ERT in patients with MPS I.
鞘内酶替代疗法(ERT)有望成为治疗溶酶体贮积病中枢神经系统表现的一种方法。通过脑脊液进行治疗是一种将重组酶输送穿过血脑屏障的潜在方法。在I型、II型和IIIA型黏多糖贮积症(MPS)动物模型中进行的实验表明,通过鞘内途径给予的ERT可在整个中枢神经系统中分布并穿透脑组织,在脑组织中它可促进溶酶体贮积物质的清除。目前正在进行研究以调查鞘内ERT治疗I型MPS患者的安全性和有效性。