Kimber I, Moore M
J Clin Lab Immunol. 1981 Jan;5(1):41-6.
Cell-mediated haemolysis of human erythrocytes (HRBC) mediated by sensitizing alloantibodies of two specificities was studied using the 51Cr release assay. Peripheral blood mononuclear cells (PBMC) were found capable fo lysing HRBC of phenotype ARh(D) + ve sensitized with either anti-D or "natural" anti-A antibodies. The characteristics of the effector population, however, were dependent upon the sensitizing antibody. HRBC sensitized with anti-A were lysed by a radioresistant, silica- and carrageenan-sensitive population which could be selectively removed by adherence. Sensitization with rhesus antibody induced cytotoxicity by a population which was radiosensitive and relatively unaffected by removal of adherent cells or by treatment with silica or carrageenan. The results demonstrate that the antigen-antibody interaction, rather than the target cell type, determines which effector cells participate in antibody-dependent cellular cytotoxicity (ADCC) against human red cells.
利用51Cr释放试验研究了由两种特异性致敏同种抗体介导的人红细胞(HRBC)的细胞介导溶血。发现外周血单个核细胞(PBMC)能够裂解用抗-D或“天然”抗-A抗体致敏的ARh(D)阳性表型的HRBC。然而,效应细胞群体的特征取决于致敏抗体。用抗-A致敏的HRBC被一个对辐射有抗性、对二氧化硅和角叉菜胶敏感的群体裂解,该群体可通过黏附选择性去除。用恒河猴抗体致敏诱导细胞毒性的群体对辐射敏感,去除黏附细胞或用二氧化硅或角叉菜胶处理对其影响相对较小。结果表明,抗原-抗体相互作用而非靶细胞类型决定了哪些效应细胞参与针对人红细胞的抗体依赖性细胞毒性(ADCC)。