MyD88-dependent immune activation mediated by human immunodeficiency virus type 1-encoded Toll-like receptor ligands

J Virol. 2007 Aug;81(15):8180-91. doi: 10.1128/JVI.00421-07. Epub 2007 May 16.

Abstract

Immune activation is a major characteristic of human immunodeficiency virus type 1 (HIV-1) infection and a strong prognostic factor for HIV-1 disease progression. The underlying mechanisms leading to immune activation in viremic HIV-1 infection, however, are not fully understood. Here we show that, following the initiation of highly active antiretroviral therapy, the immediate decline of immune activation is closely associated with the reduction of HIV-1 viremia, which suggests a direct contribution of HIV-1 itself to immune activation. To propose a mechanism, we demonstrate that the single-stranded RNA of HIV-1 encodes multiple uridine-rich Toll-like receptor 7/8 (TLR7/8) ligands that induce strong MyD88-dependent plasmacytoid dendritic cell and monocyte activation, as well as accessory cell-dependent T-cell activation. HIV-1-encoded TLR ligands may, therefore, directly contribute to the immune activation observed during viremic HIV-1 infection. These data provide an initial rationale for inhibiting the TLR pathway to directly reduce the chronic immune activation induced by HIV-1 and the associated immune pathogenesis.

Publication types

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

MeSH terms

  • Animals
  • Antigens, CD / immunology
  • Antiretroviral Therapy, Highly Active
  • Biomarkers / metabolism
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Cells, Cultured
  • HIV Infections / immunology
  • HIV Infections / therapy
  • HIV-1 / genetics
  • HIV-1 / immunology*
  • Humans
  • Immune System / physiology*
  • Interleukin-6 / immunology
  • Ligands
  • Macrophages / cytology
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Differentiation Factor 88 / genetics
  • Myeloid Differentiation Factor 88 / metabolism*
  • Oligonucleotides / genetics
  • Oligonucleotides / immunology
  • RNA, Viral / metabolism
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology*
  • Tumor Necrosis Factor-alpha / immunology
  • Uridine / metabolism
  • Viremia

Substances

  • Antigens, CD
  • Biomarkers
  • Interleukin-6
  • Ligands
  • Myeloid Differentiation Factor 88
  • Oligonucleotides
  • RNA, Viral
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha
  • Uridine