Campos M, Rossi C R
Vet Immunol Immunopathol. 1987 Apr;14(4):297-307. doi: 10.1016/0165-2427(87)90033-x.
Bovine peripheral blood mononuclear leukocytes (PBML) were stimulated in vitro with the mitogenic lectins concanavalin A (Con A) and phytohemagglutinin. Their cytotoxic capabilities were evaluated in a 51Cr release assay. Lectin-activated bovine effector cells did not mediate antibody dependent cellular cytotoxicity (ADCC) nor direct killing against cultured tumor target cells. Nevertheless, activation of PBML with lectins consistently generated effector cells able to mediate lectin-dependent cellular cytotoxicity. Cultivation of Con A stimulated-PBML for 3 to 4 weeks in the presence of lymphokines-containing IL-2 generated cells with the ability to mediate lysis without using Con A-coated target cells. However, cytotoxic cultures capable of mediating direct lysis of target cells were not able to mediate ADCC.
用促有丝分裂凝集素刀豆球蛋白A(Con A)和植物血凝素在体外刺激牛外周血单个核白细胞(PBML)。在51Cr释放试验中评估它们的细胞毒性能力。凝集素激活的牛效应细胞既不介导抗体依赖性细胞毒性(ADCC),也不直接杀伤培养的肿瘤靶细胞。然而,用凝集素激活PBML始终能产生能够介导凝集素依赖性细胞毒性的效应细胞。在含有白细胞介素-2的淋巴因子存在下,将Con A刺激的PBML培养3至4周,产生的细胞能够在不使用Con A包被靶细胞的情况下介导细胞裂解。然而,能够介导靶细胞直接裂解的细胞毒性培养物不能介导ADCC。