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J Virol, May 1998, p. 3720-3728, Vol. 72, No. 5
SyStemix, Inc., Palo Alto, California 94304
Received 2 December 1997/Accepted 29 January 1998
We have studied retroviral transgene expression in primary human
lymphocytes. Our data demonstrate that transgene expression is high in
activated primary CD4+ T cells but significantly decreased
in mitotically quiescent cells. Incorporation of a DNA fragment from
the scaffold attachment region (SAR) of the human beta interferon gene
into the vector improved transgene expression, particularly in
quiescent cells. The SAR element functioned in an orientation-dependent
manner and enhanced expression of Moloney murine leukemia virus- and murine embryonic stem cell-based vectors. Clonal analysis of transduced T cells showed that the SAR sequence did not confer
position-independent expression on a transgene but rather prevented the
decrease of expression when cells became quiescent. The SAR sequence
also enhanced transgene expression in T cells generated from
retrovirally transduced CD34-enriched hematopoietic progenitor-stem
cells in a SCID-hu thymus-liver mouse model. We have used the
SAR-containing retroviral vector to express the RevM10 gene, a
trans-dominant mutant of the human immunodeficiency virus
type 1 (HIV-1) Rev gene. Compared to a standard retroviral vector, the
SAR-containing vector was up to 2 orders of magnitude more efficient in
inhibiting replication of the HIV-1 virus in infected CD4+
peripheral blood lymphocyte populations in vitro. This is the first
demonstration that SAR elements can be used to improve retroviral vector expression in human primary T cells.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Scaffold Attachment Region-Mediated Enhancement of
Retroviral Vector Expression in Primary T Cells
*
Corresponding author. Mailing address: Systemix, Inc.,
3155 Porter Dr., Palo Alto, CA 94304. Phone: (650) 813-5071. Fax: (650) 813-5101. E-mail: iplavec{at}stem.com.
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