| Literature DB >> 17657413 |
Yugang Wang1, Leiming Guo, Kunpeng Zhao, Jugao Chen, Jiannan Feng, Yingxun Sun, Yan Li, Beifen Shen.
Abstract
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.Entities:
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Year: 2007 PMID: 17657413 DOI: 10.1007/s10529-007-9478-3
Source DB: PubMed Journal: Biotechnol Lett ISSN: 0141-5492 Impact factor: 2.461