Human immunodeficiency virus type 1 (HIV-1) uses a coreceptor together with CD 1 to enter CD4(+) target cells. The chemokine receptors CXCR4 and CCR5 have been found to be the major coreceptors for T-cell line-tropic and macrophagetropic HIV-1 strains, respectively, although many other chemokine and orphan receptors have also been identified as potential coreceptors for HIV-1. Genetic analyses has revealed the importance of chemokine and chemokine receptor genes in disease progression. The discovery of coreceptors provides a more defined scheme for virus entry in which the HIV-1 envelope glycoprotein sequentially binds CD4 and coreceptor, leading to a membrane fusion reaction between the viral envelope and the plasma membrane of the target cell. It also provides the basis for HIV-1 cell tropism. The identification of HN coreceptors provides new opportunities for the development of anti-HIV therapy. Many coreceptor-based therapeutic approaches have been developed, some of which are currently in clinical trials. Int J Hematol. 2000;72:412-417. (C)2000 The Japanese Society of Hematology.
机构:Harvard Univ, Sch Med, Charles A Dana Res Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
Wyatt, R
Kwong, PD
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Desjardins, E
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Sweet, RW
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Robinson, J
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Sodroski, JG
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机构:Harvard Univ, Sch Med, Charles A Dana Res Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
Wyatt, R
Kwong, PD
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Sweet, RW
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Robinson, J
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