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      Availability of activated CD4+ T cells dictates the level of viremia in naturally SIV-infected sooty mangabeys.

      The Journal of clinical investigation
      Animals, Antigens, CD14, biosynthesis, Antigens, CD3, CD4-Positive T-Lymphocytes, cytology, virology, Cell Proliferation, Cercocebus atys, blood, metabolism, Immunohistochemistry, Immunophenotyping, In Situ Hybridization, Models, Biological, Mucous Membrane, Receptors, Antigen, T-Cell, Simian immunodeficiency virus, Viral Load, Viremia

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          Abstract

          Naturally SIV-infected sooty mangabeys (SMs) remain asymptomatic despite high virus replication. Elucidating the mechanisms underlying AIDS resistance of SIV-infected SMs may provide crucial information to better understand AIDS pathogenesis. In this study, we assessed the determinants of set-point viremia in naturally SIV-infected SMs, i.e., immune control of SIV replication versus target cell limitation. We depleted CD4+ T cells in 6 naturally SIV-infected SMs by treating with humanized anti-CD4 mAb (Cdr-OKT4A-huIgG1). CD4+ T cells were depleted almost completely in blood and BM and at variable levels in mucosal tissues and LNs. No marked depletion of CD14+ monocytes was observed. Importantly, CD4+ T cell depletion was associated with a rapid, significant decline in viral load, which returned to baseline level at day 30-45, coincident with an increased fraction of proliferating and activated CD4+ T cells. Throughout the study, virus replication correlated with the level of proliferating CD4+ T cells. CD4+ T cell depletion did not induce any changes in the fraction of Tregs or the level of SIV-specific CD8+ T cells. Our results suggest that the availability of activated CD4+ T cells, rather than immune control of SIV replication, is the main determinant of set-point viral load during natural SIV infection of SMs.

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