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通过多表位疫苗设计方法对抗尼帕病毒:一种针对致命病毒的潜在预防解决方案。

Designing of a multi-epitope vaccine candidate against Nipah virus by approach: a putative prophylactic solution for the deadly virus.

机构信息

Discipline of Biosciences and Biomedical Engineering, Indian Institute of Technology Indore, Indore, Simrol, Indore, India.

出版信息

J Biomol Struct Dyn. 2021 Mar;39(4):1461-1480. doi: 10.1080/07391102.2020.1734088. Epub 2020 Mar 4.

Abstract

Nipah virus (NPV) is one of the most notorious viruses with a very high fatality rate. Because of the recurrent advent of this virus and its severe neurological implications, often leading to high mortality, the WHO R&D Blueprint, 2018 has listed the Nipah virus as one of the emerging infectious diseases requiring urgent research and development effort. Yet there is a major layback in the development of effective vaccines or drugs against NPV. In this study, we have designed a stable multivalent vaccine combining several T-cell and B-cell epitopes of the essential Nipah viral proteins with the help of different ligands and adjuvants which can effectively induce both humoral and cellular immune responses in human. Different advanced immune-informatic tools confirm the stability, high immunogenicity and least allergenicity of the vaccine candidate. The standard molecular dynamic cascade analysis validates the stable interaction of the vaccine construct with the human Toll-like receptor 3 (TLR3) complex. Later, codon optimization and cloning in a known pET28a vector system shows the possibility for the expression of this vaccine in a simple organism like . It is believed that with further and validation, this vaccine construct can pose to be a better prophylactic solution to the Nipah viral disease. Communicated by Ramaswamy H. Sarma.

摘要

尼帕病毒(NPV)是一种死亡率非常高的极具危害性的病毒。由于这种病毒经常出现且具有严重的神经影响,通常导致高死亡率,因此,世界卫生组织研发蓝图(2018 年)已将尼帕病毒列为需要紧急研究和开发努力的新出现传染病之一。然而,针对 NPV 的有效疫苗或药物的开发却存在重大阻碍。在这项研究中,我们设计了一种稳定的多价疫苗,该疫苗结合了几种尼帕病毒重要蛋白的 T 细胞和 B 细胞表位,并辅以不同的配体和佐剂,能够有效地在人类中诱导体液和细胞免疫反应。不同的先进免疫信息学工具证实了候选疫苗的稳定性、高免疫原性和最低的变应原性。标准分子动力学级联分析验证了疫苗构建体与人类 Toll 样受体 3(TLR3)复合物的稳定相互作用。随后,对密码子进行优化并在已知的 pET28a 载体系统中进行克隆,表明该疫苗在像 这样的简单生物体中表达的可能性。人们相信,通过进一步的 和 验证,这种疫苗构建体可能成为尼帕病毒病更好的预防解决方案。由拉玛斯瓦米·H·萨玛传达。

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