Optimal conditions for lentiviral transduction of engrafting human CD34+ cells-Reference-Cited by-同舟云学术

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Optimal conditions for lentiviral transduction of engrafting human CD34+ cells

Published:2011-05-05 Issue:11 Volume:18 Page:1078-1086
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Uchida N,Hsieh M M,Hayakawa J,Madison C,Washington K N,Tisdale J F

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/gt201163.pdf

Reference47 articles.

1. Hacein-Bey-Abina S, Le Deist F, Carlier F, Bouneaud C, Hue C, De Villartay JP et al. Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy. N Engl J Med 2002; 346: 1185–1193.

2. Aiuti A, Cattaneo F, Galimberti S, Benninghoff U, Cassani B, Callegaro L et al. Gene therapy for immunodeficiency due to adenosine deaminase deficiency. N Engl J Med 2009; 360: 447–458.

3. May C, Rivella S, Callegari J, Heller G, Gaensler KM, Luzzatto L et al. Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin. Nature 2000; 406: 82–86.

4. Imren S, Payen E, Westerman KA, Pawliuk R, Fabry ME, Eaves CJ et al. Permanent and panerythroid correction of murine beta thalassemia by multiple lentiviral integration in hematopoietic stem cells. Proc Natl Acad Sci USA 2002; 99: 14380–14385.

5. Levasseur DN, Ryan TM, Pawlik KM, Townes TM . Correction of a mouse model of sickle cell disease: lentiviral/antisickling beta-globin gene transduction of unmobilized, purified hematopoietic stem cells. Blood 2003; 102: 4312–4319.

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