Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/38566
Title: alpha-L-iduronidase gene-based therapy using the phiC31 system to treat mucopolysaccharidose type I mice
Authors: Stilhano, Roberta Sessa [UNIFESP]
Martin, Priscila Keiko Matsumoto [UNIFESP]
Melo, Suely Maymone de [UNIFESP]
Samoto, Vivian Yochiko [UNIFESP]
Peres, Giovani Bravin [UNIFESP]
Michelacci, Yara Maria [UNIFESP]
Silva, Flavia Helena da [UNIFESP]
Pereira, Vanessa Gonçalves [UNIFESP]
D'Almeida, Vania [UNIFESP]
Cruz, Adriana Taveira da [UNIFESP]
Jasiulionis, Miriam Galvonas [UNIFESP]
Han, Sang Won [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Keywords: gene therapy
IDUA
mucopolysaccharidose type I
phiC31 integrase
Issue Date: 1-Jan-2015
Publisher: Wiley-Blackwell
Citation: Journal of Gene Medicine. Hoboken: Wiley-Blackwell, v. 17, n. 1-2, p. 1-13, 2015.
Abstract: BackgroundMucopolysaccharidose type I (MPSI) is a lysosomal monogenic disease caused by mutations in the gene for - l-iduronidase (IDUA). MPSI patients need a constant supply of IDUA to alleviate progression of the disease. IDUA gene transfer using integrative vectors might provide a definitive solution and support advancement to clinical trials, although studies have not yet been satisfactory. To achieve a stable IDUA gene expression in vivo, phiC31 was tested in the present study.MethodsSeveral plasmid vectors were constructed and IDUA-/- mice were treated with cyclophosphamide and transfected with these vectors hydrodynamically via tail veins. IDUA expression was monitored over time. Treated and nontreated mice underwent an open-field test at age 8 months, and IDUA activity and glycosaminoglycan (GAG) content of tissues were evaluated.ResultsHigh levels of IDUA activity were detected initially (>1000 U/ml), although these levels decayed over time. the reinjection of vectors produced a similar profile of IDUA decay. Three out of six treated mice had IDUA activity in the livers, and also showed lower GAG content, reduced lysosomes and better locomotion. To investigate unsustained IDUA production, wild-type mice were submitted to the same gene therapy procedure, which generated a similar profile of IDUA decay. Anti-IDUA antibody was detected in the sera of these animals. in addition, we also found three methylated sites in the cytomegalovirus promoter region.ConclusionsphiC31-mediated gene therapy resulted in an important improvement in IDUA-/- mice, including locomotion, although the obstacles that need to be overcome to enable long-term gene therapy for MPSI are also noted. Copyright (c) 2015 John Wiley & Sons, Ltd.
URI: http://repositorio.unifesp.br/handle/11600/38566
ISSN: 1099-498X
Other Identifiers: http://dx.doi.org/10.1002/jgm.2818
Appears in Collections:Em verificação - Geral

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