Sex-specific innate immune selection of HIV-1 in utero is associated with increased female susceptibility to infection

Nat Commun. 2020 Apr 14;11(1):1767. doi: 10.1038/s41467-020-15632-y.

Abstract

Female children and adults typically generate more efficacious immune responses to vaccines and infections than age-matched males, but also suffer greater immunopathology and autoimmune disease. We here describe, in a cohort of > 170 in utero HIV-infected infants from KwaZulu-Natal, South Africa, fetal immune sex differences resulting in a 1.5-2-fold increased female susceptibility to intrauterine HIV infection. Viruses transmitted to females have lower replicative capacity (p = 0.0005) and are more type I interferon-resistant (p = 0.007) than those transmitted to males. Cord blood cells from females of HIV-uninfected sex-discordant twins are more activated (p = 0.01) and more susceptible to HIV infection in vitro (p = 0.03). Sex differences in outcome include superior maintenance of aviraemia among males (p = 0.007) that is not explained by differential antiretroviral therapy adherence. These data demonstrate sex-specific innate immune selection of HIV associated with increased female susceptibility to in utero infection and enhanced functional cure potential among infected males.

Publication types

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

MeSH terms

  • Anti-Retroviral Agents / therapeutic use
  • Cohort Studies
  • Female
  • HIV Infections / drug therapy
  • HIV Infections / immunology*
  • HIV Infections / metabolism
  • HIV-1 / drug effects
  • HIV-1 / immunology*
  • HIV-1 / pathogenicity*
  • Humans
  • Immunity, Innate / genetics
  • Immunity, Innate / physiology*
  • Infectious Disease Transmission, Vertical
  • Interferons / metabolism
  • Kaplan-Meier Estimate
  • Male
  • Phylogeny
  • Sex Factors
  • Translational Research, Biomedical

Substances

  • Anti-Retroviral Agents
  • Interferons