Abstract
Immunovirological consequences of a switch to a maraviroc/raltegravir dual therapy were analyzed in 16 HIV-infected patients with persistent viral load below 50 copies/ml. At 26-week postswitch, the CD4/CD8 ratio decreased and the CD8 T-cell activation increased. A decrease in classical monocytes was associated with a shift toward a proinflammatory monocyte profile and negatively correlated with ultrasensitive viral load. Thus, this therapeutic switch induced a proinflammatory profile probably driven by a slight loss of virus control.
MeSH terms
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Anti-HIV Agents / therapeutic use*
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CD4-CD8 Ratio
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CD4-Positive T-Lymphocytes / immunology
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CD8-Positive T-Lymphocytes / immunology
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Cyclohexanes / therapeutic use*
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Female
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HIV Infections / drug therapy*
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HIV Infections / immunology*
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Humans
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Lymphocyte Activation
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Male
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Maraviroc
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Middle Aged
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Monocytes / immunology
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RNA, Viral / blood
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Raltegravir Potassium / therapeutic use*
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Treatment Outcome
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Triazoles / therapeutic use*
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Viral Load*
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Viremia*
Substances
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Anti-HIV Agents
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Cyclohexanes
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RNA, Viral
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Triazoles
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Raltegravir Potassium
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Maraviroc