Elevated binding activity of CD8+ cells with phytohaemagglutinin by asbestos fibre in vitro
Corresponding Author
K. KINUGAWA
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Dr K. Kinugawa, Department of Hygiene, Kawasaki Medical School, 577 Matsushima, Kurashiki, Japan.Search for more papers by this authorF. HYODOH
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorA. ANDOH
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorA. UEKI
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorH. TANAKA
Department of Urology, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorY. MOCHIZUKI
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorCorresponding Author
K. KINUGAWA
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Dr K. Kinugawa, Department of Hygiene, Kawasaki Medical School, 577 Matsushima, Kurashiki, Japan.Search for more papers by this authorF. HYODOH
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorA. ANDOH
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorA. UEKI
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorH. TANAKA
Department of Urology, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorY. MOCHIZUKI
Department of Hygiene, Kawasaki Medical School, Matsushima, Kurashiki, Japan
Search for more papers by this authorSUMMARY
Asbestos fibres are known to depress the mitogenic stimuli of phytohaemagglutinin (PHA) to lymphocytes. We examined effects of asbestos (chrysotile) fibre on the proliferation of PHA-stimulated lymphocytes and the PHA binding activity of lymphocytes in vitro. The incorporation of 3H-thymidine and the expression of interleukin-2 receptor were depressed when the cells were exposed to 50 μg/ml of chrysotile fibre. The PHA binding activity of lymphocytes was significantly enhanced after chrysotile fibre exposure, as compared with non-exposed group. These results indicate that the depression of PHA stimuli with chrysotile fibre was not due to blocking of PHA binding to lymphocytes. The enhancement of PHA binding activity by chrysotile fibre was observed on CD8+ but not on CD4+ cells. It is possible, therefore, that treatment of peripheral blood mononuclear cells with chrysotile fibre induces increased reactivity of CDS+ cells with PHA, and that intensely activated CD8+ cells suppress proliferation of lymphocytes.
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