单结构域抗体在体外和体内中和登革病毒的研究。

Q3 Medicine
Surbhi Dahiya, Sudhakar Singh, Gaurav Kumar Bhati, Sharvan Sehrawat
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引用次数: 0

摘要

为了减轻抗体依赖性增强在DenV发病机制中的作用,我们从内部构建的骆驼VHH噬菌体展示库中获得了DenV中和单域抗体(sdAb)。抗DenV sdAb与DenV包膜(E)蛋白特异性反应,Kd值为2x108。分子动力学模拟和对接分析表明,sdAb通过结构域II (EDII)与DenV(E)蛋白相互作用,干扰病毒内化过程。抗DenV(E) sdAb在体外能有效抑制表达DenV(E)蛋白的假病毒的感染性,也能抑制致病性DenV的感染性。适应DenV2的小鼠在感染的IFNRKO小鼠中诱导100%的死亡率,但注射了sdAb中和病毒的动物仍然完全受到保护。此外,治疗性给予抗DenV(E) sdAb减缓疾病进展并提高DenV感染动物的存活率。总之,我们报告了一种抗DenV(E) sdAb作为控制DenV发病机制的潜在治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro and in vivo neutralization of Dengue virus by a single domain antibody.

To alleviate the contribution of antibody dependent enhancement in DenV pathogenesis, we obtain a DenV neutralizing single domain antibody (sdAb) from an in-house constructed phage display library of camelid VHH. The anti-DenV sdAb specifically reacts with the envelope (E) protein of DenV with a Kd value of 2x108. Molecular dynamic simulations and docking analysis show that the sdAb interacts with the DenV(E) protein via domain II (EDII) and interferes with the virus internalization process. The anti-DenV(E) sdAb potently inhibits the infectivity of a DenV(E) protein expressing pseudovirus as well as that of a virulent DenV in vitro. A mouse adapted DenV2 induces 100% mortality in the infected IFNRKO mice, but the animals injected with the sdAb neutralized virus remain fully protected. Furthermore, the therapeutically administered anti-DenV(E) sdAb slows down the disease progression and enhances the survival of DenV infected animals. In conclusion, we report an anti-DenV(E) sdAb as a potential therapy to manage DenV pathogenesis.

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来源期刊
CiteScore
3.70
自引率
0.00%
发文量
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审稿时长
4 weeks
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