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Journal of Virology, February 1999, p. 1528-1534, Vol. 73, No. 2
Division of Hematology/Oncology, Department
of Medicine, University of California, San Francisco, School of
Medicine, San Francisco, California 94143
Received 4 September 1998/Accepted 11 November 1998
All human immunodeficiency virus (HIV) isolates can grow readily in
primary CD4+ T cells, but they can be distinguished by
their ability to replicate in macrophages and established T-cell lines.
The macrophage-tropic viruses are generally non-syncytium inducing
(NSI), whereas the T-cell-line-tropic viruses are syncytium inducing
(SI) in cultured cells. We now demonstrate that infection of
CD4+ T cells by NSI and SI viruses shows a differential
effect on production of
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Differential Effects of Human Immunodeficiency
Virus Isolates on
-Chemokine and Gamma Interferon Production
and on Cell Proliferation

-chemokines and gamma interferon. Infection
by NSI viruses increased production of MIP-1
, MIP-1
, and gamma interferon, whereas infection by SI viruses had no effect or decreased production of these cytokines. Production of RANTES was slightly increased during infection by both virus phenotypes. This differential effect of NSI and SI viruses was observed at the level of
-chemokine mRNA as well as at the level of protein expression. Infection by NSI
viruses also increased CD4+ cell proliferation. These
results may have relevance for a differential role of HIV strains in
AIDS pathogenesis.
*
Corresponding author. Mailing address: Division of
Hematology/Oncology, Department of Medicine, University of California, San Francisco, School of Medicine, San Francisco, CA 94143. Phone: (415) 476-4071. Fax: (415) 476-8365.
Present address: The Mount Sinai Medical Center, New York, N.Y.
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