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Human Gene Therapy
Retroviral Infection Is Limited by Brownian Motion
To cite this article:
A. S. Chuck, M. F. Clarke, B. O. Palsson.
Human Gene Therapy.
August 1996,
7(13): 1527-1534.
doi:10.1089/hum.1996.7.13-1527.
A. S. Chuck1,3 M. F. Clarke2 Address reprint requests to: Dr. Bernhard O. Palsson, Department of Bioengineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412 04 01 1996 Received for publication January 4, 1996. 13 05 1996 Accepted after revision May 13, 1996. ABSTRACT Replication-defective retroviruses are frequently used as gene carriers for gene transfer into target cells. Here we show that the short half-lives of retroviruses limit the distance that they can effectively travel in solution by Brownian motion, and thus the possibility of successful gene transfer. This physicochemical limitation can be overcome, and effective contact between the retroviral gene carrier and the target cell can be obtained, by using net convective flow of retrovirus-containing medium through a layer of target cells. Using model cell lines (NIH-3T3 and CV-1), it was shown that gene transfer rates can be increased by more than an order of magnitude using the same concentration infection medium. High transduction rates could be obtained even in the absence of polycations, such as Polybrene, which heretofore have been required to achieve reasonable transduction rates. This development may play an important role in realizing human gene therapy. Overview summary Retroviruses have short half-lives and therefore can only travel a limited distance by random Brownian motion in infection medium before deactivating. This distance is only a few hundred microns, and this constraint is shown to limit gene transfer rates. This limitation can be overcome by slow flow of the infection medium vertically through the target cell bed and gene transfer rates can be substantially increased.  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