Schistosoma mansoni infection cancels the susceptibility to Plasmodium chabaudi through induction of type 1 immune responses in A/J mice

Int Immunol. 2000 Aug;12(8):1117-25. doi: 10.1093/intimm/12.8.1117.

Abstract

Susceptibility to Plasmodium chabaudi depends on the relative dominance of T(h)1/T(h)2 responses in host mice. A T(h)2-dominant response during the early phase of infection in susceptible A/J mice causes a fatal disease course due to severe malaria. Schistosoma mansoni is a potent inducer of a T(h)2-dominant response not only to the parasite antigens, but also to other antigens concurrently existing in the host animals. In spite of S. mansoni infection, these A/J mice escape death from malaria and showed accompanied enhanced production of IFN-gamma to malaria antigens. Treatment with anti-IFN-gamma mAb in S. mansoni-infected A/J mice abolished the resistance to malaria, indicating that IFN-gamma was responsible for the resistance to P. chabaudi in S. mansoni-infected A/J mice. Results in this study show that under certain circumstances, S. mansoni infection can promote type 1 immune responses in A/J mice that normally develop T(h)2 responses.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibiosis*
  • Antibodies, Monoclonal / pharmacology
  • Antigens, Protozoan / immunology*
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Genetic Predisposition to Disease
  • HSP90 Heat-Shock Proteins / biosynthesis
  • HSP90 Heat-Shock Proteins / genetics
  • Immunity, Innate
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology
  • Interleukin-10 / antagonists & inhibitors
  • Interleukin-10 / immunology
  • Mice
  • Mice, Inbred A / genetics
  • Mice, Inbred A / immunology*
  • Mice, Inbred C57BL
  • Plasmodium chabaudi / immunology*
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Schistosoma mansoni / immunology*
  • Schistosomiasis mansoni / immunology*
  • Spleen / immunology
  • Th1 Cells / immunology
  • Th2 Cells / immunology

Substances

  • Antibodies, Monoclonal
  • Antigens, Protozoan
  • Cytokines
  • HSP90 Heat-Shock Proteins
  • RNA, Messenger
  • Interleukin-10
  • Interferon-gamma