Wang Yugang, Guo Leiming, Zhao Kunpeng, Chen Jugao, Feng Jiannan, Sun Yingxun, Li Yan, Shen Beifen
Institute of Basic Medical Sciences, Beijing, PR China.
Biotechnol Lett. 2007 Dec;29(12):1811-6. doi: 10.1007/s10529-007-9478-3. Epub 2007 Jul 27.
So far, no specific therapeutic agent is available for the treatment of ricin intoxication. Here, V(H) and V(L) genes were cloned from a hybridoma cell line secreting anti-ricin mAb 4C13, which could neutralize the toxicity of ricin. A chimeric antibody, c4C13, containing 4C13 mAb variable region genes fused to human constant region genes (gamma 1, kappa), was constructed. C4C13 retained the binding activity and recognized the same, or a closely related, epitope as the original mouse antibody. Furthermore, c4C13 blocked ricin-induced cytotoxicity to SP2/0 cells. Compared with its parental mouse antibody, c4C13 will be safer when used in human body to reverse clinical ricin intoxication.
到目前为止,尚无用于治疗蓖麻毒素中毒的特效治疗药物。在此,从分泌抗蓖麻毒素单克隆抗体4C13的杂交瘤细胞系中克隆了V(H)和V(L)基因,该抗体可中和蓖麻毒素的毒性。构建了一种嵌合抗体c4C13,它包含与人类恒定区基因(γ1,κ)融合的4C13单克隆抗体可变区基因。C4C13保留了结合活性,识别与原始小鼠抗体相同或密切相关的表位。此外,c4C13可阻断蓖麻毒素对SP2/0细胞的细胞毒性。与亲本小鼠抗体相比,c4C13用于人体逆转临床蓖麻毒素中毒时将更安全。