Abstract
Using a 51Cr release assay, we investigated Fas-mediated cytotoxicity of peripheral blood CD4+ T cells of patients with human T-lymphotropic virus type-I (HTLV-I)-associated myelopathy (HAM) against T98G, a glioblastoma cell line which expresses Fas. Cytotoxic activity of CD4+ T cells against T98G was significantly higher in HAM patients than in controls. Moreover, when CD4+ T cells of HAM patients were preincubated with a monoclonal antibody to human Fas ligand (FasL), cytotoxic activity against T98G was significantly suppressed. These results suggest that damage to nervous tissues by the Fas/FasL system is involved in the pathogenesis of HAM.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aged
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Antibodies, Monoclonal
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CD4-Positive T-Lymphocytes / chemistry
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CD4-Positive T-Lymphocytes / immunology*
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CD4-Positive T-Lymphocytes / virology*
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Chromium Radioisotopes
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Cytotoxicity Tests, Immunologic
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Female
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Glioblastoma
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Humans
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Immunoglobulin M
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Middle Aged
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Paraparesis, Tropical Spastic / immunology*
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Paraparesis, Tropical Spastic / metabolism
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T-Lymphocytes, Cytotoxic / immunology
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Tumor Cells, Cultured / chemistry
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Tumor Cells, Cultured / immunology
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Tumor Cells, Cultured / metabolism
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fas Receptor / immunology*
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fas Receptor / metabolism
Substances
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Antibodies, Monoclonal
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Chromium Radioisotopes
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Immunoglobulin M
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fas Receptor