Intrathecal enzyme replacement therapy: Successful treatment of brain disease via the cerebrospinal fluid

被引:142
作者
Dickson, Patricia
McEntee, Michael
Vogler, Carole
Le, Steven
Levy, Beth
Peinovich, Maryn
Hanson, Stephen
Passage, Merry
Kakkis, Emil
机构
[1] Univ Calif Los Angeles, Dept Pediat, Div Med Genet, LA Biomed Harbor, Torrance, CA 90502 USA
[2] Univ Tennessee, Coll Vet Med, Dept Pathobiol, Knoxville, TN 37901 USA
[3] St Louis Univ, Dept Pathol, St Louis, MO 63103 USA
[4] Vet Neurosci Ctr, Tustin, CA USA
[5] BioMarin Pharmaceut Inc, Novato, CA USA
关键词
mucopolysaccharidosis I; lysosomal storage disorder; intrathecal; enzyme replacement therapy; central nervous system; cerebrospinal fluid; Hurler; Scheie; Hurler-Scheie; pachymeningitis;
D O I
10.1016/j.ymgme.2006.12.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 idu-ronidase (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. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:61 / 68
页数:8
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