Semi-automated closed system manufacturing of lentivirus gene-modified haematopoietic stem cells for gene therapy-Reference-Cited by-同舟云学术

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Semi-automated closed system manufacturing of lentivirus gene-modified haematopoietic stem cells for gene therapy

Published:2016-10-20 Issue:1 Volume:7 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Adair Jennifer E.,Waters Timothy,Haworth Kevin G.,Kubek Sara P.,Trobridge Grant D.,Hocum Jonah D.,Heimfeld Shelly,Kiem Hans-Peter

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms13173.pdf

Reference32 articles.

1. Ghosh, S., Thrasher, A. J. & Gaspar, H. B. Gene therapy for monogenic disorders of the bone marrow. Br. J. Haematol. 171, 155–170 (2015)).

2. Naldini, L. Ex vivo gene transfer and correction for cell-based therapies. Nat. Rev. Genet. 12, 301–315 (2011).

3. Burtner, C. R. et al. Intravenous injection of a foamy virus vector to correct canine SCID-X1. Blood 123, 3578–3584 (2014).

4. Kay, M. A. et al. In vivo gene therapy of hemophilia B: sustained partial correction in factor IX-deficient dogs. Science 262, 117–119 (1993).

5. Ponder, K. P. et al. Therapeutic neonatal hepatic gene therapy in mucopolysaccharidosis VII dogs. Proc. Natl Acad. Sci. USA 99, 13102–13107 (2002).

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