Literature DB >> 18549329

Laronidase (Aldurazyme): enzyme replacement therapy for mucopolysaccharidosis type I.

Gregory M Pastores1.   

Abstract

BACKGROUND: Laronidase (Aldurazyme) is a recombinant formulation of alpha-L-iduronidase, the enzyme deficient in mucopolysaccharidosis type I (MPS-I); a disorder associated with skeletal dysplasia, restricted joint movement, short stature, obstructive pulmonary disease, cardiac valvular problems and cognitive impairment (in the severe and intermediate variants).
OBJECTIVE: To describe MPS-I and review data on the safety and efficacy of laronidase.
RESULTS: Laronidase is safe and effective in stabilizing or improving pulmonary function and physical endurance. As intravenously administered enzyme is unable to correct CNS disease, hematopoietic stem cell transplantation remains the primary treatment for Hurler's syndrome despite the morbidity and mortality risks.
CONCLUSIONS: Palliative care remains part of the treatment. Long-term studies are required to ascertain the effect of enzyme therapy on survival and its effectiveness in modifying the disease course and reducing morbidity. Intrathecal administration is under investigation for patients with signs of cord compression secondary to glycosaminoglycan accumulation within the dura matter. The cost of therapy remains a concern.

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Year:  2008        PMID: 18549329     DOI: 10.1517/14712598.8.7.1003

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  6 in total

1.  Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model.

Authors:  Ilaria Visigalli; Stefania Delai; Letterio S Politi; Carmela Di Domenico; Federica Cerri; Emanuela Mrak; Raffaele D'Isa; Daniela Ungaro; Merel Stok; Francesca Sanvito; Elisabetta Mariani; Lidia Staszewsky; Claudia Godi; Ilaria Russo; Francesca Cecere; Ubaldo Del Carro; Alessandro Rubinacci; Riccardo Brambilla; Angelo Quattrini; Paola Di Natale; Katherine Ponder; Luigi Naldini; Alessandra Biffi
Journal:  Blood       Date:  2010-09-16       Impact factor: 22.113

2.  Engineering a lysosomal enzyme with a derivative of receptor-binding domain of apoE enables delivery across the blood-brain barrier.

Authors:  Daren Wang; Salim S El-Amouri; Mei Dai; Chia-Yi Kuan; David Y Hui; Roscoe O Brady; Dao Pan
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

3.  Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study.

Authors:  L Borgwardt; C I Dali; J Fogh; J E Månsson; K J Olsen; H C Beck; K G Nielsen; L H Nielsen; S O E Olsen; H M F Riise Stensland; O Nilssen; F Wibrand; A M Thuesen; T Pearl; U Haugsted; P Saftig; J Blanz; S A Jones; A Tylki-Szymanska; N Guffon-Fouiloux; M Beck; A M Lund
Journal:  J Inherit Metab Dis       Date:  2013-03-14       Impact factor: 4.982

Review 4.  Cognitive outcomes and age of detection of severe mucopolysaccharidosis type 1.

Authors:  Scott D Grosse; Wendy K K Lam; Lisa D Wiggins; Alex R Kemper
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

5.  Liver-Directed Human Amniotic Epithelial Cell Transplantation Improves Systemic Disease Phenotype in Hurler Syndrome Mouse Model.

Authors:  Natalie S Rodriguez; Lisa Yanuaria; Kevin Murphy R Parducho; Irving M Garcia; Bino A Varghese; Brendan H Grubbs; Toshio Miki
Journal:  Stem Cells Transl Med       Date:  2017-06-06       Impact factor: 6.940

6.  Chronic enzyme replacement therapy ameliorates neuropathology in alpha-mannosidosis mice.

Authors:  Markus Damme; Stijn Stroobants; Meike Lüdemann; Michelle Rothaug; Renate Lüllmann-Rauch; Hans Christian Beck; Annika Ericsson; Claes Andersson; Jens Fogh; Rudi D'Hooge; Paul Saftig; Judith Blanz
Journal:  Ann Clin Transl Neurol       Date:  2015-09-19       Impact factor: 4.511

  6 in total

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