Lentiviral vector gene therapy: effective and safe?
- PMID: 20436489
- PMCID: PMC2890097
- DOI: 10.1038/mt.2010.70
Lentiviral vector gene therapy: effective and safe?
Comment in
-
Assessing the risk of T-cell malignancies in mouse models of SCID-X1.Mol Ther. 2010 May;18(5):868-70. doi: 10.1038/mt.2010.69. Mol Ther. 2010. PMID: 20436493 Free PMC article. No abstract available.
References
-
- Aiuti A., and , Roncarolo MG. Ten years of gene therapy for primary immune deficiencies. Hematology Am Soc Hematol Educ Program. 2009;288:682–689. - PubMed
-
- Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, Gross F, Yvon E, Nusbaum P, et al. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science. 2000;288:669–672. - PubMed
-
- Aiuti A, Slavin S, Aker M, Ficara F, Deola S, Mortellaro A, et al. Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning. Science. 2002;296:2410–2413. - PubMed
-
- Hacein-Bey-Abina S, Von Kalle C, Schmidt M, McCormack MP, Wulffraat N, Leboulch P, et al. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1. Science. 2003;302:415–419. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
