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发现一种人源单克隆抗体,能中和眼镜蛇蛇毒的致死性。

discovery of a human monoclonal antibody that neutralizes lethality of cobra snake venom.

机构信息

Department of Biotechnology and Biomedicine, Technical University of Denmark, Kongens Lyngby, Denmark.

IONTAS Ltd .; Cambridgeshire, United Kingdom.

出版信息

MAbs. 2022 Jan-Dec;14(1):2085536. doi: 10.1080/19420862.2022.2085536.

DOI:10.1080/19420862.2022.2085536
PMID:35699567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9225616/
Abstract

The monocled cobra () is among the most feared snakes in Southeast Asia due to its toxicity, which is predominantly derived from long-chain α-neurotoxins. The only specific treatment for snakebite envenoming is antivenom based on animal-derived polyclonal antibodies. Despite the lifesaving importance of these medicines, major limitations in safety, supply consistency, and efficacy create a need for improved treatments. Here, we describe the discovery and subsequent optimization of a recombinant human monoclonal immunoglobulin G antibody against α-cobratoxin using phage display technology. Affinity maturation by light chain-shuffling resulted in a significant increase in neutralization potency and efficacy. The optimized antibody prevented lethality when incubated with whole venom prior to intravenous injection. This study is the first to demonstrate neutralization of whole snake venom by a single recombinant monoclonal antibody, thus providing a tantalizing prospect of bringing recombinant antivenoms based on human monoclonal or oligoclonal antibodies to the clinic.

摘要

单环眼镜蛇()是东南亚地区最令人恐惧的蛇类之一,因为其毒性主要来自长链α-神经毒素。唯一针对蛇咬伤中毒的特定治疗方法是基于动物源性多克隆抗体的抗蛇毒血清。尽管这些药物具有救生的重要性,但在安全性、供应一致性和疗效方面存在重大限制,这就需要改进治疗方法。在这里,我们描述了使用噬菌体展示技术发现并随后优化针对α-眼镜蛇毒素的重组人源单克隆 IgG 抗体的过程。通过轻链改组进行亲和力成熟,显著提高了中和效力和功效。该优化抗体在静脉注射前与全毒液孵育时可预防致死性。这项研究首次证明了单克隆抗体能够中和整个蛇毒,这为将基于人源单克隆或寡克隆抗体的重组抗蛇毒血清推向临床提供了诱人的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/1b85216efec2/KMAB_A_2085536_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/9d2f80f5ccd5/KMAB_A_2085536_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/6653af31b6e7/KMAB_A_2085536_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/593e2d626b88/KMAB_A_2085536_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/a6d05ecaaa98/KMAB_A_2085536_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/1b85216efec2/KMAB_A_2085536_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/9d2f80f5ccd5/KMAB_A_2085536_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/6653af31b6e7/KMAB_A_2085536_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/593e2d626b88/KMAB_A_2085536_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/a6d05ecaaa98/KMAB_A_2085536_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1966/9225616/1b85216efec2/KMAB_A_2085536_F0005_OC.jpg

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