Cell-mediated cytotoxicity toward human lymphocytes: comparison between in vivo immunization and in vitro sensitization.
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Biomedical subjects
Publications and source records attributed to L Legrand.
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Erythrocyte group antigens A and B can act as potent and group-specific transplantation antigens in man. ABO group-incompatible recipients pretreated with such antigens have rejected skin allografts obtained from donors incompatible for the same antigens in an accelerated (4-5 days) or white graft manner. Skin grafts applied to the same recipients from ABO-compatible donors were accorded first-set survival times. Intact erythrocyte suspensions and antigens isolated from hog (A substance) and horse (B substance) stomachs, were equally capable of inducing this type of allograft sensitivity. The latter observation broadens the spectrum of heterologous antigens capable of inducing allograft sensitivity in the mammalian host and provides a readily available, heat-stable, and water-soluble source of antigens for further studies of allograft rejection mechanisms in man.
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Incubation of human peritoneal macrophages with cell free supernatants of mixed human lymphocyte cultures (MLC) renders them cytotoxic to labelled target tumour cells. The factor responsible for this effect is found as early as the second day of MLC. The production of this factor in man does not seem to require previous sensitization. In contrast with observations in mice, we have not yet demonstrated in man any clear-cut difference between the macrophage cytotoxicity index observed with supernatants from normal MLC and from MLC between the donor and the recipient of a skin allograft. Human blood monocytes can also be rendered cytotoxic by MLC acellular supernatants, but their cytotoxicity is neither as consistent nor as strong as with macrophages. This human factor does not render mouse macrophages cytotoxic.
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