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Journal of Virology, December 2001, p. 11284-11291, Vol. 75, No. 23
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.23.11284-11291.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Reducing the Native Tropism of Adenovirus Vectors
Requires Removal of both CAR and Integrin Interactions
David A.
Einfeld,*
Rosanna
Schroeder,
Peter W.
Roelvink,
Alena
Lizonova,
C.
Richter
King,
Imre
Kovesdi, and
Thomas J.
Wickham
GenVec, Inc., Gaithersburg, Maryland 20878
Received 19 April 2001/Accepted 21 August 2001
The development of tissue-selective virus-based
vectors requires a better understanding of the role of receptors in
gene transfer in vivo, both to rid the vectors of their native tropism
and to introduce new specificity. CAR and
v integrins have been
identified as the primary cell surface components that interact with
adenovirus type 5 (Ad5)-based vectors during in vitro transduction. We
have constructed a set of four vectors, which individually retain the wild-type cell interactions, lack CAR binding, lack
v integrin binding, or lack both CAR and
v integrin binding. These vectors have
been used to examine the roles of CAR and
v integrin in determining
the tropism of Ad vectors in a mouse model following intrajugular or
intramuscular injection. CAR was found to play a significant role in
liver transduction. The absence of CAR binding alone, however, had
little effect on the low level of expression from Ad in other tissues.
Binding of
v integrins appeared to have more influence than did
binding of CAR in promoting the expression in these tissues and was
also found to be important in liver transduction by Ad vectors. An
effect of the penton base modification was a reduction in the number of
vector genomes that could be detected in several tissues. In the liver,
where CAR binding is important, combining defects in CAR and
v
integrin binding was essential to effectively reduce the high level of
expression from Ad vectors. While there may be differences in Ad vector
tropism among species, our results indicate that both CAR and
v
integrins can impact vector distribution in vivo. Disruption of both
CAR and
v integrin interactions may be critical for effectively
reducing native tropism and enhancing the efficacy of specific
targeting ligands in redirecting Ad vectors to target tissues.
*
Corresponding author. Mailing address: GenVec, Inc., 65 W. Watkins Mill Rd., Gaithersburg, MD 20878. Phone: (240) 632-5545. Fax: (240) 632-0736. E-mail: deinfeld{at}genvec.com.
Journal of Virology, December 2001, p. 11284-11291, Vol. 75, No. 23
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.23.11284-11291.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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