Alpha/beta interferons increase host resistance to murine AIDS

J Virol. 1996 Jul;70(7):4517-22. doi: 10.1128/JVI.70.7.4517-4522.1996.

Abstract

Murine AIDS (MAIDS) is caused by a defective retrovirus present in the LP-BM5 murine leukemia virus mixture. Strains of inbred mice differ in resistance to MAIDS development; some are susceptible (e.g., C57BL/6), while others are resistant (e.g., CBA and B10.BR). As an early block to viral replication in resistant mice has been demonstrated previously by PCR studies, we postulated that alpha/beta interferons (IFN-alpha/beta) may be involved in resistance to MAIDS. Susceptible C57BL/6 mice infected with LP-BM5 were treated with IFN-alpha/beta or Newcastle disease virus. Newcastle disease virus induces high endogenous IFN-alpha/beta production in mice. Both treatments delayed the development of MAIDS, as assessed by splenomegaly and T- and B-cell proliferation. In addition, an IFN-alpha/beta response was detected by reverse transcription-PCR and dot blotting 3, 6, and 9 h after LP-BM5 infection in resistant mice but not in susceptible mice. These results suggest that the ability to produce IFN-alpha/beta in response to LP-BM5 infection may contribute to host resistance to MAIDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cells, Cultured
  • DNA, Viral
  • Female
  • Immunity, Innate / immunology
  • Interferon-alpha / immunology*
  • Interferon-alpha / therapeutic use
  • Interferon-beta / immunology*
  • Interferon-beta / therapeutic use
  • Leukemia Virus, Murine / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Molecular Sequence Data
  • Murine Acquired Immunodeficiency Syndrome / immunology*
  • Spleen / cytology
  • Spleen / immunology

Substances

  • DNA, Viral
  • Interferon-alpha
  • Interferon-beta