IFN-beta impairs superoxide-dependent parasite killing in human macrophages: evidence for a deleterious role of SOD1 in cutaneous leishmaniasis

J Immunol. 2009 Feb 15;182(4):2525-31. doi: 10.4049/jimmunol.0802860.

Abstract

Type I IFNs (IFN-alpha/beta) have only recently gained considerable attention as immunomodulators in nonviral infectious diseases. IFN-beta has been shown to protect, in a NO-dependent manner, against murine Old World leishmaniasis caused by Leishmania major, but data in New World leishmaniasis are lacking. We found that IFN-beta dose-dependently increases parasite burden in Leishmania amazonensis- as well as Leishmania braziliensis-infected human macrophages, independent of endogenous or exogenous NO. However, IFN-beta significantly reduced superoxide release in Leishmania-infected as well as uninfected human macrophages. This decrease in superoxide production was paralleled by a significant IFN-beta-mediated increase in superoxide dismutase 1 (SOD1) protein levels. Additionally, IFN-beta inhibition of leishmanicidal activity was mimicked by SOD1 and antagonized by either pharmacological or small interfering RNA-mediated inhibition of SOD1. Finally, pronounced SOD1 expression in situ was demonstrated in biopsies from New World cutaneous leishmaniasis patients. These findings reveal a hitherto unknown IFN-beta/SOD1 axis in Leishmania infection and suggest that inhibition of SOD-associated pathways could serve as strategy in the treatment of L. amazonensis as well as L. braziliensis infection, major human pathogens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Humans
  • Immunohistochemistry
  • Interferon-beta / immunology*
  • Leishmaniasis, Cutaneous / immunology*
  • Leishmaniasis, Cutaneous / metabolism
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / parasitology
  • Nitric Oxide / immunology
  • Nitric Oxide / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superoxide Dismutase / immunology*
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1
  • Superoxides / immunology*
  • Superoxides / metabolism

Substances

  • SOD1 protein, human
  • Superoxides
  • Nitric Oxide
  • Interferon-beta
  • Superoxide Dismutase
  • Superoxide Dismutase-1