Abstract
The discovery of chemokine receptors as HIV-1 entry molecules or "coreceptors" has lead to a greater understanding of how HIV-1 infects human cells. This has provided insight into the biological properties of HIV-1 isolates and unravelled the meaning of the syncytium-inducing and non-syncytium-inducing phenotypes. Understanding how HIV-1 exploits these coreceptors has given way to novel approaches to controlling HIV. As a result a new class of drugs has emerged that are being tested to prevent virus infection and to act as an alternative, or adjunct, to existing anti-retroviral drugs for HIV-infected individuals.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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CD4 Antigens / metabolism
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Genetic Variation
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HIV Envelope Protein gp120 / genetics
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HIV Envelope Protein gp120 / metabolism
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HIV Envelope Protein gp41 / metabolism
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HIV-1 / classification
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HIV-1 / physiology*
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Humans
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Phenotype
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Receptors, CCR5 / chemistry
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Receptors, CCR5 / metabolism
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Receptors, CXCR4 / chemistry
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Receptors, CXCR4 / metabolism
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Receptors, Cytokine / physiology*
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Receptors, HIV / physiology*
Substances
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CD4 Antigens
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HIV Envelope Protein gp120
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HIV Envelope Protein gp41
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Receptors, CCR5
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Receptors, CXCR4
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Receptors, Cytokine
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Receptors, HIV