1. Early T-cell apoptosis and Fas expression during antiretroviral therapy in individuals infected with human immunodeficiency virus-1.
- Author
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Aries SP, Weyrich K, Schaaf B, Hansen F, Dennin RH, and Dalhoff K
- Subjects
- Adult, Anti-HIV Agents therapeutic use, Drug Therapy, Combination, Female, HIV Infections drug therapy, HIV Infections virology, HIV Protease Inhibitors therapeutic use, Humans, Male, Middle Aged, Reverse Transcriptase Inhibitors therapeutic use, Time Factors, Viral Load, Apoptosis, CD4-Positive T-Lymphocytes cytology, CD8-Positive T-Lymphocytes cytology, HIV Infections immunology, HIV-1 immunology, fas Receptor biosynthesis
- Abstract
Several lines of evidence suggest that Fas-mediated apoptosis is involved in the CD4 T-cell depletion in human immunodeficiency virus-1 (HIV-1) infection. To investigate this, we studied changes in peripheral blood, early T-cell apoptosis and Fas expression after initiation of antiretroviral therapy (ART) in 18 HIV-1-infected individuals. Flow cytometric analysis was performed with Apostain and CD4, CD8 and Fas staining. Fas expression was quantified by standardized beads. The levels of CD4 and CD8 T cells with early apoptosis were increased comparably in HIV-1-infected individuals. Despite elevated CD4 T cell counts, no decline in early T-cell apoptosis could be detected during the first 8 weeks of ART. However, after 26 weeks of ART in five patients that showed a sustained reduction of viral replication there was a marked decrease in T cells with features of early apoptosis. No difference was found for Fas expression on early apoptotic T cells. Fas expression on CD4 and CD8 T cells was reduced after initiation of ART; this was independent of the CD4 T-cell trend and indicates that the immediate CD4 T-cell expansion during ART is probably not the result of a decreased rate of early apoptosis among peripheral blood CD4 T cells. However, preliminary data imply a long-term reduction of early T-cell apoptosis and Fas expression in patients who show a sustained reduction of viral replication.
- Published
- 1998
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