| Literature DB >> 21614584 |
Ursula Matte1, Valeska Lizzi Lagranha, Talita Giacomet de Carvalho, Fabiana Quoos Mayer, Roberto Giugliani.
Abstract
Lysosomal storage disorders (LSD) are monogenic diseases caused by the deficiency of different lysosomal enzymes that degrade complex substrates such as glycosaminoglycans, sphingolipids, and others. As a consequence there is multisystemic storage of these substrates. Most treatments for these disorders are based in the fact that most of these enzymes are soluble and can be internalized by adjacent cells via mannose-6-phosphate receptor. In that sense, these disorders are good candidates to be treated by somatic gene therapy based on cell microencapsulation. Here, we review the existing data about this approach focused on the LSD treatments, the advantages and limitations faced by these studies.Entities:
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Year: 2011 PMID: 21614584 DOI: 10.1007/s10545-011-9350-4
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982