Minden P, Brunda M J, Ferguson H R
J Immunol. 1978 Nov;121(5):1933-8.
Complete or partial protection against the line-10 hepatocarcinoma was conferred to a significant number of strain-2 guinea pigs by the passive transfer of antibodies reactive to antigens from line-10 cells. Immunoglobulins were administered intradermally and injected sites were subsequently challenged with line-10 cells. Immunoglobulins prepared from the sera of rabbits that had been immunized to line-10 cells and from the sera of guinea pigs that had been rendered immune to this tumor by previously described methods were more effective than immunoglobulins obtained from normal rabbit or guinea pig sera. Protection was abolished if immunoglobulins were absorbed with line-10 cells. Antitumor effects were dependent on the close contact of antibodies and tumor cells. Protection was greater if normal syngeneic peritoneal exudate cells were transferred in addition to the immunoglobulins. A possible mechanism for the antitumor effects observed is that of antibody-dependent cellular cytotoxicity.
通过被动转移对10号线肝癌细胞抗原具有反应性的抗体,相当数量的2号品系豚鼠获得了对10号线肝癌的完全或部分保护。将免疫球蛋白皮内注射,随后在注射部位用10号线细胞进行攻击。用已免疫10号线细胞的兔血清制备的免疫球蛋白,以及用先前描述的方法使其对该肿瘤产生免疫的豚鼠血清制备的免疫球蛋白,比从正常兔或豚鼠血清中获得的免疫球蛋白更有效。如果免疫球蛋白用10号线细胞吸收,则保护作用消失。抗肿瘤作用取决于抗体与肿瘤细胞的紧密接触。如果除免疫球蛋白外还转移正常同基因腹膜渗出细胞,则保护作用更大。观察到的抗肿瘤作用的一种可能机制是抗体依赖性细胞毒性。