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Lentivirus-mediated gene transfer of uroporphyrinogen III synthase fully corrects the porphyric phenotype in human cells.

Abstract
Congenital erythropoietic porphyria (CEP) is an inherited disease due to a deficiency in the uroporphyrinogen III synthase, the fourth enzyme of the heme biosynthesis pathway. It is characterized by accumulation of uroporphyrin I in the bone marrow, peripheral blood and other organs. The prognosis of CEP is poor, with death often occurring early in adult life. For severe transfusion-dependent cases, when allogeneic cell transplantation cannot be performed, the autografting of genetically modified primitive/stem cells may be the only alternative. In vitro gene transfer experiments have documented the feasibility of gene therapy via hematopoietic cells to treat this disease. In the present study lentiviral transduction of porphyric cell lines and primary CD34(+) cells with the therapeutic human uroporphyrinogen III synthase (UROS) cDNA resulted in both enzymatic and metabolic correction, as demonstrated by the increase in UROS activity and the suppression of porphyrin accumulation in transduced cells. Very high gene transfer efficiency (up to 90%) was achieved in both cell lines and CD34(+) cells without any selection. Expression of the transgene remained stable over long-term liquid culture. Furthermore, gene expression was maintained during in vitro erythroid differentiation of CD34(+) cells. Therefore the use of lentiviral vectors is promising for the future treatment of CEP patients by gene therapy.
AuthorsF Géronimi, E Richard, I Lamrissi-Garcia, M Lalanne, C Ged, I Redonnet-Vernhet, F Moreau-Gaudry, H de Verneuil
JournalJournal of molecular medicine (Berlin, Germany) (J Mol Med (Berl)) Vol. 81 Issue 5 Pg. 310-20 (May 2003) ISSN: 0946-2716 [Print] Germany
PMID12721665 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Uroporphyrinogen III Synthetase
Topics
  • Adult
  • Cell Culture Techniques
  • Cell Differentiation
  • Erythroblasts (metabolism)
  • Fluorescence
  • Gene Expression
  • Genetic Therapy
  • Genetic Vectors
  • Humans
  • Lentivirus (genetics)
  • Phenotype
  • Porphyria, Erythropoietic (genetics, therapy)
  • Transduction, Genetic
  • Uroporphyrinogen III Synthetase (genetics)
  • Virus Replication

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