Abstract
A possible role for human endogenous retroviruses (HERV) in the pathogenesis of MS was investigated by analyzing HERV peptides-stimulated proliferation and cytokine production in MS patients with acute (AMS) or stable (SMS) disease. HERV peptides specific-proliferation and type 1 cytokine production by peripheral blood mononuclear cells was observed in AMS but not in SMS individuals, in whom a type 2 cytokine profile dominates. HERV peptides-stimulated immune responses were modified by changes in disease expression; mediated by CD4+ T lymphocytes; and not related to HLA class II molecules. These data suggest the possibility of a pathogenic role for HERV and HERV-specific immune responses in MS.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acute Disease
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Adult
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Antigens, Viral / immunology
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Autoantibodies / immunology
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CD4-Positive T-Lymphocytes / cytology
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CD4-Positive T-Lymphocytes / metabolism
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CD8-Positive T-Lymphocytes / cytology
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CD8-Positive T-Lymphocytes / metabolism
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Cells, Cultured
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Cross Reactions
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Endogenous Retroviruses / immunology*
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Female
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Histocompatibility Antigens Class II / biosynthesis
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Humans
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Immunity, Cellular / immunology
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Interferon-gamma / biosynthesis
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Interleukin-10 / biosynthesis
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Interleukin-2 / biosynthesis
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Interleukin-4 / biosynthesis
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Male
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Multiple Sclerosis / immunology*
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Multiple Sclerosis / virology*
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Severity of Illness Index
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Tetanus Toxoid / immunology
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Tetanus Toxoid / pharmacology
Substances
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Antigens, Viral
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Autoantibodies
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Histocompatibility Antigens Class II
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Interleukin-2
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Tetanus Toxoid
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Interleukin-10
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Interleukin-4
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Interferon-gamma