Wang L M, Wan W H, Lu L J
Department of Biochemistry, Beijing Institute for Cancer Research.
Zhonghua Zhong Liu Za Zhi. 1994 Mar;16(2):83-7.
Bispecific monoclonal antibody (bsMAb), secreted by hybrid-hybridoma, has an intact 1g molecule construction with dual antigen binding specificities. bsMAb has several advantages over conventional conjugate in tumor targeting therapy: (1) The damage to both antibody and tumoricidal agents due to chemical crosslinking can be avoided. (2) The antigen modulation can be decreased due to monovalence binding of bsMAb with target antigen. (3) The binding affinity between Fc fragment of bsMAb with heterogenous heavy chains and Fc receptor is decreased, so that nonspecific distribution and side effects can be reduced. (4) The bsMAb can pretarget to tumor site, increasing the T/NT ratio and cytotoxicity. In the present study, A bsMAb with versatile adaptor was designed. In this bsMAb, one arm could react with gastric cancer-associated antigen, and the other with a hapten TNP. The bsMAb could mediate different tumoricidal agents crosslinked to TNP. A variant hybridoma 3H11-HAT(s) secreting McAb against gastric cancer was fused with spleen cells of mice immunized with KLH-TNP. After screening and subcloning, 10 hybrid-hybridomas were obtained, which secreted antibodies against both gastric cancer target cells BGC823 and BSA-TNP. By using special bridge method, only hybrid-hybridomas 6A3 (gamma 2b, mu), and 1G7 (gamma 2b, gamma 2b) were confirmed to secrete bsMAb. Further experiments showed that the bsMAb 6A3 and 1G7 could mediate different cytotoxicities, for example, Ricin-TNP, MMC-HSA-TNP and ADM-BSA-TNP. This system is useful for evaluating different tumoricidal agents in bsMAb targeting therapy, and has potential value in clinics.(ABSTRACT TRUNCATED AT 250 WORDS)
双特异性单克隆抗体(bsMAb)由杂交杂交瘤分泌,具有完整的Ig分子结构,具备双抗原结合特异性。在肿瘤靶向治疗中,bsMAb相较于传统偶联物具有多个优势:(1)可避免化学交联对抗体和杀肿瘤剂造成的损害。(2)bsMAb与靶抗原的单价结合可降低抗原调制。(3)bsMAb具有异源重链的Fc片段与Fc受体之间的结合亲和力降低,从而可减少非特异性分布和副作用。(4)bsMAb可预先靶向肿瘤部位,提高肿瘤与非肿瘤组织的比例(T/NT)以及细胞毒性。在本研究中,设计了一种具有通用衔接子的bsMAb。在这种bsMAb中,一条臂可与胃癌相关抗原反应,另一条臂与半抗原TNP反应。该bsMAb可介导与TNP交联的不同杀肿瘤剂。将分泌抗胃癌单克隆抗体的变异杂交瘤3H11-HAT(s)与用KLH-TNP免疫的小鼠脾细胞融合。经过筛选和亚克隆,获得了10个杂交杂交瘤,它们分泌针对胃癌靶细胞BGC823和BSA-TNP的抗体。通过使用特殊的桥接方法,仅确认杂交杂交瘤6A3(γ2b,μ)和1G7(γ2b,γ2b)分泌bsMAb。进一步实验表明,bsMAb 6A3和1G7可介导不同的细胞毒性,例如,蓖麻毒素-TNP、丝裂霉素-HSA-TNP和阿霉素-BSA-TNP。该系统有助于评估bsMAb靶向治疗中的不同杀肿瘤剂,在临床上具有潜在价值。(摘要截断于250字)