台湾鸡对 Trimeresurus stejnegeri 毒液蛋白的抗体。

IF 1.8 3区 医学 Q4 TOXICOLOGY
Chi-Hsin Lee, Chia-I Liu, Sy-Jye Leu, Yu-Ching Lee, Jen-Ron Chiang, Liao-Chun Chiang, Yan-Chiao Mao, Bor-Yu Tsai, Ching-Sheng Hung, Chi-Ching Chen, Yi-Yuan Yang
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引用次数: 0

摘要

背景介绍台湾常见的竹叶青毒蛇(Trimeresurus stejnegeri - TS)的毒液含有致命的血液毒素,可导致严重的中毒。马源性抗蛇毒血清是一种治疗蛇咬伤的特效药,但其生产成本较高,且存在一些不可避免的副作用。本研究的目的是帮助开发一种经济实惠、更持久的蛇咬伤治疗策略:方法:用戊二醛灭活 T. stejnegeri 毒液蛋白,使母鸡产生多克隆免疫球蛋白(IgY)抗体。在进行 IgY 结合试验后,构建了两个表达单链可变片段(scFv)抗体的抗体库,分别由短连接体或长连接体连接,用于噬菌体展示抗体技术。共进行了四轮生物筛选。然后进一步测试了所选 scFv 抗体与 TS 蛋白的结合活性和中和试验:结果:从蛋黄中纯化的 IgY 对 TS 蛋白具有特异性结合能力。这两个库分别包含 2.4 × 107 和 6.8 × 107 个抗体克隆。洗脱噬菌体滴度的增加表明,经过第二次淘洗后,抗 TS 克隆明显富集。根据筛选出的 scFv 克隆的核苷酸序列分析表明,共鉴定出 7 组短连接子和 4 组长连接子。重组的 scFvs 对 TS 毒液蛋白有显著的反应性,并与 Trimeresurus mucrosquamatus 毒液蛋白有交叉反应。在体内研究中,数据显示抗TS IgY提供了100%的保护效果,而联合scFvs则延长了注射致死量TS蛋白的小鼠的部分存活时间:鸡是以低成本生产中和抗体的绝佳宿主。噬菌体展示技术可用于生产针对蛇毒蛋白的单克隆抗体。在不久的将来,这些抗体可用于开发诊断试剂盒或作为蛇毒中毒治疗的替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chicken antibodies against venom proteins of Trimeresurus stejnegeri in Taiwan.

Background: The venom of bamboo vipers (Trimeresurus stejnegeri - TS), commonly found in Taiwan, contains deadly hemotoxins that cause severe envenomation. Equine-derived antivenom is a specific treatment against snakebites, but its production costs are high and there are some inevitable side effects. The aim of the present work is to help in the development of an affordable and more endurable therapeutic strategy for snakebites.

Methods: T. stejnegeri venom proteins were inactivated by glutaraldehyde in order to immunize hens for polyclonal immunoglobulin (IgY) antibodies production. After IgY binding assays, two antibody libraries were constructed expressing single-chain variable fragment (scFv) antibodies joined by the short or long linker for use in phage display antibody technology. Four rounds of biopanning were carried out. The selected scFv antibodies were then further tested for their binding activities and neutralization assays to TS proteins.

Results: Purified IgY from egg yolk showed the specific binding ability to TS proteins. The dimensions of these two libraries contain 2.4 × 107 and 6.8 × 107 antibody clones, respectively. An increase in the titers of eluted phage indicated anti-TS clones remarkably enriched after 2nd panning. The analysis based on the nucleotide sequences of selected scFv clones indicated that seven groups of short linkers and four groups of long linkers were identified. The recombinant scFvs showed significant reactivity to TS venom proteins and a cross-reaction to Trimeresurus mucrosquamatus venom proteins. In in vivo studies, the data demonstrated that anti-TS IgY provided 100% protective effects while combined scFvs augmented partial survival time of mice injected with a lethal amount of TS proteins.

Conclusion: Chickens were excellent hosts for the production of neutralization antibodies at low cost. Phage display technology is available for generation of monoclonal antibodies against snake venom proteins. These antibodies could be applied in the development of diagnostic kits or as an alternative for snakebite envenomation treatment in the near future.

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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Journal of Venomous Animals and Toxins including Tropical Diseases (JVATiTD) is a non-commercial academic open access publication dedicated to research on all aspects of toxinology, venomous animals and tropical diseases. Its interdisciplinary content includes original scientific articles covering research on toxins derived from animals, plants and microorganisms. Topics of interest include, but are not limited to:systematics and morphology of venomous animals;physiology, biochemistry, pharmacology and immunology of toxins;epidemiology, clinical aspects and treatment of envenoming by different animals, plants and microorganisms;development and evaluation of antivenoms and toxin-derivative products;epidemiology, clinical aspects and treatment of tropical diseases (caused by virus, bacteria, algae, fungi and parasites) including the neglected tropical diseases (NTDs) defined by the World Health Organization.
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