Evidence for the in vivo safety of insulated foamy viral vectors-Reference-Cited by-同舟云学术

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Evidence for the in vivo safety of insulated foamy viral vectors

Published:2016-12-26 Issue:3 Volume:24 Page:187-198
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Browning D L,Everson E M,Leap D J,Hocum J D,Wang H,Stamatoyannopoulos G,Trobridge G D

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

https://www.nature.com/articles/gt201688.pdf

Reference73 articles.

1. Touzot F, Moshous D, Creidy R, Neven B, Frange P, Cros G et al. Faster T-cell development following gene therapy compared with haploidentical HSCT in the treatment of SCID-X1. Blood 2015; 125: 3563–3569.

2. Kiem HP, Sellers S, Thomasson B, Morris JC, Tisdale JF, Horn PA et al. Long-term clinical and molecular follow-up of large animals receiving retrovirally transduced stem and progenitor cells: no progression to clonal hematopoiesis or leukemia. Mol Ther 2004; 9: 389–395.

3. Carbonaro DA, Zhang L, Jin X, Montiel-Equihua C, Geiger S, Carmo M et al. Preclinical demonstration of lentiviral vector-mediated correction of immunological and metabolic abnormalities in models of adenosine deaminase deficiency. Mol Ther 2014; 22: 607–622.

4. Bordignon C, Notarangelo LD, Nobili N, Ferrari G, Casorati G, Panina P et al. Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patients. Science 1995; 270: 470–475.

5. 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.

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