Abstract
Treatment of infected patients with ABT-538, an inhibitor of the protease of human immunodeficiency virus type 1 (HIV-1), causes plasma HIV-1 levels to decrease exponentially (mean half-life, 2.1 +/- 0.4 days) and CD4 lymphocyte counts to rise substantially. Minimum estimates of HIV-1 production and clearance and of CD4 lymphocyte turnover indicate that replication of HIV-1 in vivo is continuous and highly productive, driving the rapid turnover of CD4 lymphocytes.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Antiviral Agents / therapeutic use
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CD4 Lymphocyte Count / drug effects
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CD4-Positive T-Lymphocytes / cytology
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CD4-Positive T-Lymphocytes / virology*
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HIV Infections / drug therapy
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HIV Infections / immunology
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HIV Infections / virology*
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HIV Protease Inhibitors / therapeutic use
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HIV-1 / physiology*
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Humans
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Kinetics
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Ritonavir
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Viremia / drug therapy
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Viremia / virology*
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Virion / physiology
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Virus Replication*
Substances
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Antiviral Agents
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HIV Protease Inhibitors
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Ritonavir