Dickson Patricia, McEntee Michael, Vogler Carole, Le Steven, Levy Beth, Peinovich Maryn, Hanson Stephen, Passage Merry, Kakkis Emil
Division of Medical Genetics, Department of Pediatrics, LA Biomed at Harbor-UCLA, Torrance, CA 90502, USA.
Mol Genet Metab. 2007 May;91(1):61-8. doi: 10.1016/j.ymgme.2006.12.012. Epub 2007 Feb 26.
Treatment of brain disease with recombinant proteins is difficult due to the blood-brain barrier. As an alternative to direct injections into the brain, we studied whether application of high concentrations of therapeutic enzymes via intrathecal (IT) injections could successfully drive uptake across the ependyma to treat brain disease. We studied IT enzyme replacement therapy with recombinant human iduronidase (rhIDU) in canine mucopolysaccharidosis I (MPS I, Hurler syndrome), a lysosomal storage disorder with brain and meningeal involvement. Monthly or quarterly IT treatment regimens with rhIDU achieved supranormal iduronidase enzyme levels in the brain, spinal cord, and spinal meninges. All regimens normalized total brain glycosaminoglycan (GAG) storage and reduced spinal meningeal GAG storage by 58-70%. The improvement in GAG storage levels persisted three months after the final IT dose. The successful use of enzyme therapy via the CSF represents a potentially useful approach for lysosomal storage disorders.
由于血脑屏障的存在,用重组蛋白治疗脑部疾病具有一定难度。作为直接向脑部注射的替代方法,我们研究了通过鞘内注射(IT)应用高浓度治疗性酶是否能够成功驱动其穿过室管膜以治疗脑部疾病。我们在犬类黏多糖贮积症I型(MPS I,Hurler综合征)中研究了用重组人艾杜糖醛酸酶(rhIDU)进行鞘内酶替代疗法,这是一种累及脑和脑膜的溶酶体贮积症。每月或每季度用rhIDU进行鞘内治疗方案可使脑、脊髓和脊髓膜中的艾杜糖醛酸酶水平超过正常水平。所有方案均使全脑糖胺聚糖(GAG)贮积恢复正常,并使脊髓膜GAG贮积减少58 - 70%。在最后一次鞘内注射后三个月,GAG贮积水平的改善仍持续存在。通过脑脊液成功应用酶疗法代表了一种对溶酶体贮积症潜在有用的方法。