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

Virology. 2010 Sep 15;405(1):234-42. doi: 10.1016/j.virol.2010.06.001. Epub 2010 Jul 1.

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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • CD8-Positive T-Lymphocytes / physiology*
  • Epigenesis, Genetic / immunology*
  • HIV Infections / immunology*
  • HIV-1 / immunology
  • HIV-1 / physiology*
  • Histone Deacetylase 1
  • Histones
  • Humans
  • Leukocytes, Mononuclear / physiology
  • RNA Interference
  • Virus Replication / physiology*

Substances

  • Histones
  • HDAC1 protein, human
  • Histone Deacetylase 1