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Journal of Virology, March 2004, p. 2642-2647, Vol. 78, No. 5
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.5.2642-2647.2003
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109,1 Department of Pathology, University of Washington, Seattle, Washington 981952
Received 8 July 2003/ Accepted 13 November 2003
Jaagsiekte sheep retrovirus (JSRV) infects lung epithelial cells in sheep, and oncoretroviral vectors bearing JSRV Env can mediate transduction of human cells, suggesting that such vectors might be useful for lung-directed gene therapy. Here we show that JSRV Env can also efficiently pseudotype a human immunodeficiency virus type 1-based lentiviral vector, a more suitable vector for transduction of slowly dividing lung epithelial cells. We created several chimeric Env proteins that, unlike the parental Env, do not transform rodent fibroblasts but are still capable of pseudotyping lentiviral and oncoretroviral vectors.
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