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Journal of Virology, January 1999, p. 316-324, Vol. 73, No. 1
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Determinant in Human Immunodeficiency Virus Type 1 for
Efficient Replication under Cytokine-Induced CD4+
T-Helper 1 (Th1)- and Th2-Type Conditions
Youichi
Suzuki,1
Yoshio
Koyanagi,1,*
Yuetsu
Tanaka,2
Tsutomu
Murakami,1
Naoko
Misawa,1
Naoyoshi
Maeda,1
Tohru
Kimura,1
Hisatoshi
Shida,3
James A.
Hoxie,4
William A.
O'Brien,5 and
Naoki
Yamamoto1
Departments of Microbiology and Molecular
Virology, School of Medicine, Tokyo Medical and Dental University,
Bunkyo-ku, Tokyo 113-8519,1
Department
of Biosciences, School of Science, Kitasato University, Sagamihara
228-8555,2 and
Institute for Virus
Research, Kyoto University, Kyoto 606,3 Japan;
Hematology and Oncology Division, Department of Medicine,
University of Pennsylvania Medical Center, Philadelphia,
Pennsylvania 191044; and
Department of
Medicine, University of Texas Medical Branch, Galveston, Texas
775555
Received 30 March 1998/Accepted 21 September 1998
Cytokines are potent stimuli for CD4+-T-cell
differentiation. Among them, interleukin-12 (IL-12) and IL-4 induce
naive CD4+ T cells to become T-helper 1 (Th1) or Th2 cells,
respectively. In this study we found that macrophage-tropic human
immunodeficiency virus type 1 (HIV-1) strains replicated more
efficiently in IL-12-induced Th1-type cultures derived from normal
CD4+ T cells than did T-cell-line-tropic (T-tropic)
strains. In contrast, T-tropic strains preferentially infected
IL-4-induced Th2-type cultures derived from the same donor
CD4+ T cells. Additional studies using chimeric viruses
demonstrated that the V3 region of HIV-1 gp120 was the principal
determinant for efficiency of replication. Cell fusion analysis showed
that cells expressing envelope protein from a T-tropic strain
effectively fused with IL-4-induced Th2-type culture cells. Flow
cytometric analysis showed that the level of CCR5 expression was higher
on IL-12-induced Th1-type culture cells, whereas CXCR4 was highly expressed on IL-4-induced Th2-type culture cells, although a low level
of CXCR4 expression was observed on IL-12-induced Th1-type culture
cells. These results indicate that HIV-1 isolates exhibit differences
in the ability to infect CD4+-T-cell subsets such as Th1 or
Th2 cells and that this difference may partly correlate with the
expression of particular chemokine receptors on these cells. The
findings suggest that immunological conditions are one of the factors
responsible for inducing selection of HIV-1 strains.
*
Corresponding author. Mailing address: Department of
Microbiology, Tokyo Medical and Dental University, School of Medicine, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan. Phone:
81-3-5803-5181. Fax: 81-3-5803-0124. E-mail:
koyanagi.mmb{at}med.tmd.ac.jp.
Journal of Virology, January 1999, p. 316-324, Vol. 73, No. 1
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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