Berinstein N, Levy R
J Immunol. 1987 Aug 1;139(3):971-6.
A transplantable murine B cell lymphoma was used to study combination therapy with anti-idiotype antibody and interleukin 2 (IL 2). Class-switched IgG2a and IgG2b antibodies were compared. A marked additive and sometimes synergistic effect was seen when IL 2 was combined with either IgG2a or IgG2b anti-idiotype antibodies. A synergistic effect was also seen when similar experiments were performed in nude mice. In vitro antibody-dependent cellular cytotoxicity (ADCC) assays showed that IL 2 enhanced antibody-mediated lysis by peritoneal cells exposed to IL 2 in vitro in a dose-related manner. Peritoneal cells harvested from mice treated in vivo with IL 2 contained an increased number of T cells and asialo GM+ natural killer cells, and also mediated enhanced ADCC. Depletion of natural killer cells with anti-asialo GM and complement resulted in a marked decrease in the antibody-dependent cytotoxicity mediated by these peritoneal cells. The mechanism of synergy between monoclonal antibody and IL 2 may be due to the direct or indirect activation of natural killer cells mediating ADCC.
一种可移植的小鼠B细胞淋巴瘤被用于研究抗独特型抗体与白细胞介素2(IL-2)的联合治疗。对类别转换的IgG2a和IgG2b抗体进行了比较。当IL-2与IgG2a或IgG2b抗独特型抗体联合使用时,观察到显著的相加效应,有时还有协同效应。在裸鼠中进行类似实验时也观察到了协同效应。体外抗体依赖性细胞毒性(ADCC)试验表明,IL-2以剂量相关的方式增强了体外暴露于IL-2的腹腔细胞介导的抗体裂解作用。从体内用IL-2治疗的小鼠中收获的腹腔细胞含有更多数量的T细胞和脱唾液酸GM+自然杀伤细胞,并且也介导增强的ADCC。用抗脱唾液酸GM和补体清除自然杀伤细胞导致这些腹腔细胞介导的抗体依赖性细胞毒性显著降低。单克隆抗体与IL-2之间的协同机制可能是由于介导ADCC的自然杀伤细胞的直接或间接激活。