Regulatory Considerations for Novel Gene Therapy Products: A Review of the Process Leading to the First Clinical Lentiviral Vector-Reference-Cited by-同舟云学术

Regulatory Considerations for Novel Gene Therapy Products: A Review of the Process Leading to the First Clinical Lentiviral Vector

Published:2005-01 Issue:1 Volume:16 Page:17-25
ISSN:1043-0342
Container-title:Human Gene Therapy
language:en
Short-container-title:Human Gene Therapy

Author:

Manilla Peter¹,Rebello Tessio¹,Afable Cathleen¹,Lu Xiaobin¹,Slepushkin Vladimir¹,Humeau Laurent M.¹,Schonely Kathy¹,Ni Yajin¹,Binder Gwendolyn K.¹,Levine Bruce L.²,Macgregor Rob-Roy²,June Carl H.²,Dropulic Boro¹

Affiliation:

1. VIRxSYS, 200 Perry Parkway, Gaithersburg, MD 20877.

2. Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104.

Publisher

Mary Ann Liebert Inc

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/hum.2005.16.17

Reference32 articles.

1. Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone

2. Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement

3. Report to the NIH Recombinant DNA Advisory Committee on Murine Replication-Competent Retrovirus (RCR) Assays (February 17, 1993)

4. Analysis of the functional relationship between V3 loop and gp120 context with regard to human immunodeficiency virus coreceptor usage using naturally selected sequences and different viral backbones

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