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
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibiosis*
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Antibodies, Monoclonal / pharmacology
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Antigens, Protozoan / immunology*
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Cytokines / biosynthesis
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Cytokines / genetics
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Enzyme-Linked Immunosorbent Assay
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Female
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Genetic Predisposition to Disease
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HSP90 Heat-Shock Proteins / biosynthesis
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HSP90 Heat-Shock Proteins / genetics
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Immunity, Innate
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Interferon-gamma / antagonists & inhibitors
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Interferon-gamma / biosynthesis
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Interferon-gamma / genetics
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Interferon-gamma / immunology
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Interleukin-10 / antagonists & inhibitors
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Interleukin-10 / immunology
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Mice
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Mice, Inbred A / genetics
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Mice, Inbred A / immunology*
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Mice, Inbred C57BL
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Plasmodium chabaudi / immunology*
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RNA, Messenger / biosynthesis
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Reverse Transcriptase Polymerase Chain Reaction
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Schistosoma mansoni / immunology*
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Schistosomiasis mansoni / immunology*
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Spleen / immunology
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Th1 Cells / immunology
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Th2 Cells / immunology
Substances
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Antibodies, Monoclonal
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Antigens, Protozoan
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Cytokines
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HSP90 Heat-Shock Proteins
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RNA, Messenger
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Interleukin-10
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Interferon-gamma