Sex differences in the Toll-like receptor-mediated response of plasmacytoid dendritic cells to HIV-1

Nat Med. 2009 Aug;15(8):955-9. doi: 10.1038/nm.2004. Epub 2009 Jul 13.

Abstract

Manifestations of viral infections can differ between women and men, and marked sex differences have been described in the course of HIV-1 disease. HIV-1-infected women tend to have lower viral loads early in HIV-1 infection but progress faster to AIDS for a given viral load than men. Here we show substantial sex differences in the response of plasmacytoid dendritic cells (pDCs) to HIV-1. pDCs derived from women produce markedly more interferon-alpha (IFN-alpha) in response to HIV-1-encoded Toll-like receptor 7 (TLR7) ligands than pDCs derived from men, resulting in stronger secondary activation of CD8(+) T cells. In line with these in vitro studies, treatment-naive women chronically infected with HIV-1 had considerably higher levels of CD8(+) T cell activation than men after adjusting for viral load. These data show that sex differences in TLR-mediated activation of pDCs may account for higher immune activation in women compared to men at a given HIV-1 viral load and provide a mechanism by which the same level of viral replication might result in faster HIV-1 disease progression in women compared to men. Modulation of the TLR7 pathway in pDCs may therefore represent a new approach to reduce HIV-1-associated pathology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / pathology
  • Dendritic Cells / immunology*
  • Female
  • HIV Infections / blood
  • HIV Infections / immunology*
  • HIV Infections / metabolism
  • HIV-1 / immunology*
  • HIV-1 / physiology
  • Humans
  • Interferon-alpha / metabolism
  • Lymphocyte Activation / immunology
  • Male
  • Progesterone / blood
  • Sex Characteristics*
  • Toll-Like Receptor 7 / agonists
  • Toll-Like Receptor 7 / metabolism
  • Toll-Like Receptor 7 / physiology*
  • Viral Load

Substances

  • Interferon-alpha
  • TLR7 protein, human
  • Toll-Like Receptor 7
  • Progesterone