Antibody dependent cellular cytotoxicity (ADCC) against human erythrocytes, mediated by blood group alloantibodies: a model for the role of antigen density in target cell lysis.

H Northoff, A Kluge, K Resch
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Abstract

Antibody dependent cellular cytotoxicity (ADCC) of human mononuclear cells against human erythrocytes could be obtained with anti-A and anti-D sera. The degree of lysis varied considerably depending on the antigen system and on the experimental conditions. Anti-D mediated in contrast to anti-A mediated ADCC turned out to be very sensitive to conditions which interfere with target cell lysis: for most of the anti-D sera, removal of unbound IgG was found to be crucial to detect their ability to mediate ADCC. Pretreatment of the target cells with various enzymes dramatically improved specific lysis and left spontaneous release and spontaneous cytotoxicity essentially unaffected. In the case of neuraminidase treatment it could be shown that the effect was independent from the exposure of additional binding sites. When enzyme treatment and removal of excess IgG were applied in combination, as little as 10(4) antigenic determinants proved to be sufficient to induce specific lysis.

抗体依赖性细胞毒性(ADCC)对抗人红细胞,由血型同种抗体介导:抗原密度在靶细胞裂解中的作用模型。
用抗a和抗d血清可获得人单核细胞对人红细胞的抗体依赖性细胞毒性(ADCC)。裂解的程度取决于抗原系统和实验条件。与抗a介导的ADCC相比,抗d介导的ADCC对干扰靶细胞裂解的条件非常敏感:对于大多数抗d血清,去除未结合的IgG被发现是检测其介导ADCC能力的关键。用各种酶对靶细胞进行预处理,显著提高了特异性裂解,基本不影响自发释放和自发细胞毒性。在神经氨酸酶治疗的情况下,它可以表明,效果是独立于暴露额外的结合位点。当酶处理和去除多余的IgG结合使用时,只需10(4)个抗原决定因子就足以诱导特异性裂解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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