Honda S, Ichimori Y, Iwasa S
Research and Development Division, Takeda Chemical Industries, Ltd., Osaka, Japan.
Cytotechnology. 1990 Jul;4(1):59-68. doi: 10.1007/BF00148811.
By fusing a human hybridoma producing an IgG2 kappa antibody against human A431 epidermoid carcinoma cells with an Epstein-Barr virus-transformed human B lymphocyte producing an IgG2 kappa antibody against Pseudomonas aeruginosa exotoxin A, we established a hybrid hybridoma producing a bispecific monoclonal antibody reacting with both A431 cells and the exotoxin. Human IgG was purified from the culture supernatant of the hybrid hybridoma, and the bispecific monoclonal antibody in the IgG preparation was further separated from the two parental antibodies by hydroxyapatite high-performance liquid chromatography. The human bispecific monoclonal antibody thus obtained efficiently targeted the antibody-reactive cells, A431, for attack by the exotoxin in vitro.
通过将产生抗人A431表皮样癌细胞的IgG2 κ抗体的人杂交瘤与产生抗铜绿假单胞菌外毒素A的IgG2 κ抗体的爱泼斯坦-巴尔病毒转化的人B淋巴细胞融合,我们建立了一种杂交杂交瘤,其产生与A431细胞和外毒素都反应的双特异性单克隆抗体。从杂交杂交瘤的培养上清液中纯化人IgG,并且通过羟基磷灰石高效液相色谱法将IgG制剂中的双特异性单克隆抗体与两种亲本抗体进一步分离。由此获得的人双特异性单克隆抗体在体外有效地将抗体反应性细胞A431作为外毒素攻击的靶标。