Virus entry as a target for anti-HIV intervention.

Abstract

The replicative cycle of the human immunodeficiency virus (HIV) can be interrupted at several stages. Until recently only the viral reverse transcriptase and protease were the only enzymes targeted by antiretroviral agents. However, the first HIV entry inhibitor (T-20, Enfuvirtide, Fuseon) to be used in humans has been approved by the Food and Drug Administration (FDA). The HIV entry process is considered as an attractive target for chemotherapeutic intervention, as blocking HIV entry into its target cell leads to suppression of viral infectivity, replication and the cytotoxicity induced by virus-cell contacts. HIV-1 entry into target cells is a multistep process: virus attachment is initiated by the binding of trimeric envelope glycoprotein gp120 complexes on the virions to glycosylated T-cell surface receptor (CD4) and HIV GPCR coreceptors (CCR5 or CXCR4) leading to envelope glycoprotein gp41-dependent fusion-pore formation and membrane fusion. A number of compounds are being developed to specifically target each of these steps leading to virus entry and some compounds have reached early clinical development. Conversely, agents such as the CCR5 antagonist Tak-779 and the CXCR4 antagonist AMD3100 are not longer being thought as relevant anti-HIV agents but have given way to new analogues with improved properties. This review summarizes the current state of HIV entry inhibitors, their mechanisms of action and their therapeutic value against HIV infection and AIDS.

• Authors: José A Esté
• Journal: Current medicinal chemistry (Curr Med Chem) Vol. 10 Issue 17 Pg. 1617-32 (Sep 2003) ISSN: 0929-8673 [Print] United Arab Emirates
• PMID: 12871111 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Anti-HIV Agents
• CD4 Antigens
• HIV Envelope Protein gp120
• HIV Envelope Protein gp41
• HIV Fusion Inhibitors
• Receptors, HIV

Topics

• Anti-HIV Agents (pharmacology, therapeutic use)
• CD4 Antigens (drug effects, metabolism)
• Cell Adhesion (drug effects)
• Cell Membrane (virology)
• HIV Envelope Protein gp120 (drug effects, metabolism)
• HIV Envelope Protein gp41 (drug effects, metabolism)
• HIV Fusion Inhibitors (pharmacology)
• HIV-1 (drug effects, pathogenicity)
• Humans
• Receptors, HIV (antagonists & inhibitors, drug effects, metabolism)