Arunachalam B, Ghosh S, Talwar G P, Raghupathy R
National Institute of Immunology, Shahid Jeet Singh Marg, New Delhi, India.
Hybridoma. 1992 Apr;11(2):165-79. doi: 10.1089/hyb.1992.11.165.
Protective human monoclonal antibodies (HuMAbs) are superior to hyperimmune sera and murine monoclonal antibodies as far as human immunotherapy is concerned. In this report, we describe the successful generation of triomas secreting HuMAbs to tetanus toxin (tt). Lymphoblastoid cell lines secreting anti-tt antibodies were stabilized by back-fusion with a mouse x human heterohybrid myeloma partner, SBC-H20. One of the antibodies so produced, confers total protection of mice from tetanus, unlike a few recent reports where only partial protection (delay in the onset of tetanus) was achieved with single HuMAbs. Experiments to localize the neutralizing epitope(s) of the toxin using the protective monoclonal antibodies revealed that the antibody recognizes a conformational determinant that is destroyed on SDS-treatment. Preliminary studies show that Fab preparations of the protective antibody are capable of neutralizing tetanus toxin, suggesting that it might be possible to clone and express the Fab in a stable vector for large scale production.
就人类免疫疗法而言,保护性人源单克隆抗体(HuMAbs)优于超免疫血清和鼠源单克隆抗体。在本报告中,我们描述了成功产生分泌针对破伤风毒素(tt)的HuMAbs的三瘤细胞。分泌抗tt抗体的淋巴母细胞系通过与小鼠x人异源杂交骨髓瘤伙伴SBC-H20反向融合而得以稳定。如此产生的一种抗体能使小鼠完全免受破伤风感染,这与最近一些报告不同,那些报告中使用单个HuMAbs仅实现了部分保护(破伤风发作延迟)。利用保护性单克隆抗体定位毒素中和表位的实验表明,该抗体识别一个在SDS处理后被破坏的构象决定簇。初步研究表明,保护性抗体的Fab制剂能够中和破伤风毒素,这表明有可能在稳定载体中克隆并表达Fab以进行大规模生产。