Journal of Virology, December 1998, p. 10323-10327, Vol. 72, No. 12
Laboratory of Virology, Istituto Superiore di
Sanità, Viale Regina Elena 299, 00161 Rome, Italy
Received 29 June 1998/Accepted 26 August 1998
In this article, we show that passage in SCID mice rendered a human
CD4+ T-cell line (CEM cells) highly susceptible to
infection by macrophage-tropic (M-tropic) strains and primary clinical
isolates of human immunodeficiency virus type 1 (HIV-1). This in
vivo-acquired permissiveness of CEM cells was associated with the
induction of a CD45RO+ phenotype as well as of some
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Human Lymphoblastoid CD4+ T Cells
Become Permissive to Macrophage-Tropic Strains of Human
Immunodeficiency Virus Type 1 after Passage into Severe Combined
Immunodeficient Mice through In Vivo Upregulation of CCR5: In Vivo
Dynamics of CD4+ T-Cell Differentiation in Pathogenesis
of AIDS
-chemokine receptors. Regulated upon activation, normal T-cell
expressed and secreted chemokine entirely inhibited the ability of
M-tropic HIV-1 strains to infect these cells. These findings may lead
to new approaches in investigating in vivo the capacity of different
HIV strains to exploit chemokine receptors in relation to the dynamics
of the activation and/or differentiation state of human
CD4+ T cells.
*
Corresponding author. Mailing address: Laboratory of
Virology, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy. Phone: 396 49903294. Fax: 396 49387184. E-mail:
Fais{at}iss.it.
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