Abstract

The replication of human immunodeficiency virus type 1 (HIV-1) can be inhibited by noncytolytic CD8+ T cell mediated suppression, an immune response that specifically targets HIV-1 gene expression. Clinical studies demonstrate that this immune response may play an important role in the host defense against HIV infection. In this study, we examined the distinct steps in viral gene expression for inhibition by noncytolytic CD8+ T cells. A primary HIV-1 infection system of CD4+ enriched peripheral blood mononuclear cells was utilized to examine the HIV-1 life cycle as a relevant ex vivo system. Established CD8+ T cell lines from two HIV+ long-term nonprogressors were used to examine differences at the level of transcriptional initiation and elongation of the HIV genome. This infection system coupled with the results from real-time measurement of newly transcribed RNA transcripts determined that there was a significant decrease (5-8 fold) in short intracellular viral RNA transcripts. These data strongly favor a role for the initiation of virus transcription in noncytolytic CD8+ T cell mediated suppression.

Highlights

  • The concept of non-cytolytic CD8+ T cell mediated suppression of human immunodeficiency virus type 1 (HIV-1) unfolded in a seminal study by Levy’s group [1] that showed that CD8+ T lymphocytes can inhibit HIV replication in a dose dependent manner

  • To examine the mechanism of noncytolytic CD8+ T cell mediated suppression during the time of viral gene expression, we utilized a single cycle infection assay in primary CD4+ lymphocytes

  • This system allows the isolated study of the effects of noncytolytic CD8+ suppression on HIV replication in a system where we have previously measured the kinetics of HIV entry, reverse transcription and early gene expression [21]

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Summary

Introduction

The concept of non-cytolytic CD8+ T cell mediated suppression of HIV-1 unfolded in a seminal study by Levy’s group [1] that showed that CD8+ T lymphocytes can inhibit HIV replication in a dose dependent manner. A significant number of exposed uninfected individuals demonstrate noncytolytic CD8+ T cell mediated suppressive activity [12, 13] These clinical studies indicate that CD8+ T cell mediated antiviral activity may play an important role in the host defense against HIV infection and have a great potential to be of use in vaccination strategies. These results will contribute to the goal of identifying the specific antiviral mechanisms, and viral and cellular components, that contribute to the control of viremia by noncytolytic CD8+ T cell suppression

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