Epigenetic regulation of CD8+ T-lymphocyte mediated suppression of HIV-1 replication

Abstract

CD8+ T-lymphocytes from HIV-1 infected individuals express unidentified factors that suppress viral replication by inhibiting HIV-1 gene expression. We examined the role of epigenetics in modulating the HIV-1 suppressive factors expressed by primary CD8+ T cells from subjects naturally controlling virus replication. HIV-1 suppression by CD8+ T-lymphocytes was reversed up to 40% by the addition of a histone deacetylase (HDAC) inhibitor. Noncytolytic suppression was not dependent on epigenetic changes within the target cells, as HDAC1 within the target cell was dispensable, and HIV-1 LTR histone acetylation remained unchanged in the presence of CD8+ T-lymphocytes. Histone deacetylation within CD8+ T-lymphocytes was necessary for potent HIV-1 suppression. Blocking HDACs impairs the ability of CD8+ T-lymphocytes to repress HIV-1 transcription, demonstrating that expression of a portion of the suppressive factors is regulated by epigenetics. These data provide a way to focus the search for the suppressive factors and to potentially modulate their expression.