DeMonte L B, Nistico P, Tecce R, Dellabona P, Momo M, Anichini A, Mariani M, Natali P G, Malavasi F
Dipartimento di Genetica, Biologia e Chimica Medica, Università di Torino, Turin, Italy.
Proc Natl Acad Sci U S A. 1990 Apr;87(8):2941-5. doi: 10.1073/pnas.87.8.2941.
The present study reports on the use of gene transfer by retrovirus-derived shuttle vectors in the generation of hybrid hybridomas secreting bispecific monoclonal antibodies. neo- and dhfr- genes were infected into distinct murine hybridomas, thus conferring a dominant resistance trait to geneticin (G418) and to methotrexate. The vectors employed were replication-deficient and dependent on complementation by a helper virus provided by the irradiated packaging lines. After cocultivation with the relevant packaging cell lines, stable hybridoma lines expressing the selectable markers were easily obtained and were then suitable for conventional somatic fusion. This high-efficiency method was used to generate two bispecific monoclonal antibodies simultaneously targeting molecules expressed on cytotoxic cells (i.e., T lymphocytes and natural killer cells) against a human melanoma-associated antigen.
本研究报告了利用源自逆转录病毒的穿梭载体进行基因转移,以产生分泌双特异性单克隆抗体的杂交杂交瘤。将新霉素基因和二氢叶酸还原酶基因导入不同的小鼠杂交瘤中,从而赋予对遗传霉素(G418)和甲氨蝶呤的显性抗性特征。所使用的载体是复制缺陷型的,依赖于由经辐射的包装细胞系提供的辅助病毒进行互补。与相关包装细胞系共培养后,很容易获得表达选择标记的稳定杂交瘤细胞系,然后适用于常规体细胞融合。这种高效方法被用于同时产生两种双特异性单克隆抗体,它们靶向细胞毒性细胞(即T淋巴细胞和自然杀伤细胞)上表达的分子,针对一种人类黑色素瘤相关抗原。