Inferring B-cell derived T-cell receptor induced multi-epitope-based vaccine candidate against enterovirus 71: a reverse vaccinology approach.

IF 2.1 Q4 IMMUNOLOGY Clinical and Experimental Vaccine Research Pub Date : 2024-04-01 Epub Date: 2024-04-30 DOI:10.7774/cevr.2024.13.2.132
Subrat Kumar Swain, Subhasmita Panda, Basanta Pravas Sahu, Soumya Ranjan Mahapatra, Jyotirmayee Dey, Rachita Sarangi, Namrata Misra
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Abstract

Purpose: Enterovirus 71, a pathogen that causes hand-foot and mouth disease (HFMD) is currently regarded as an increasing neurotropic virus in Asia and can cause severe complications in pediatric patients with blister-like sores or rashes on the hand, feet, and mouth. Notwithstanding the significant burden of the disease, no authorized vaccine is available. Previously identified attenuated and inactivated vaccines are worthless over time owing to changes in the viral genome.

Materials and methods: A novel vaccine construct using B-cell derived T-cell epitopes from the virulent polyprotein found the induction of possible immune response. In order to boost the immune system, a beta-defensin 1 preproprotein adjuvant with EAAAK linker was added at the N-terminal end of the vaccine sequence.

Results: The immunogenicity of the designed, refined, and verified prospective three-dimensional-structure of the multi-epitope vaccine was found to be quite high, exhibiting non-allergenic and antigenic properties. The vaccine candidates bound to toll-like receptor 3 in a molecular docking analysis, and the efficacy of the potential vaccine to generate a strong immune response was assessed through in silico immunological simulation.

Conclusion: Computational analysis has shown that the proposed multi-epitope vaccine is possibly safe for use in humans and can elicit an immune response.

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推断 B 细胞衍生 T 细胞受体诱导的多表位肠道病毒 71 型候选疫苗:一种反向疫苗学方法。
目的:肠道病毒 71 是一种导致手足口病(HFMD)的病原体,目前在亚洲被认为是一种日益严重的神经性病毒,可导致儿童患者出现严重并发症,手、足和口腔出现水疱样溃疡或皮疹。尽管手足口病的发病率很高,但目前还没有获得授权的疫苗。由于病毒基因组的变化,以前确定的减毒疫苗和灭活疫苗随着时间的推移已失去价值:材料和方法:一种新型疫苗结构使用了来自毒性多聚蛋白的 B 细胞衍生 T 细胞表位,可诱导可能的免疫反应。为了增强免疫系统,在疫苗序列的 N 端添加了带有 EAAAK 连接器的 beta-defensin 1 前蛋白佐剂:结果:经设计、改进和验证的多表位前瞻性三维结构疫苗具有很高的免疫原性,表现出非过敏性和抗原性。在分子对接分析中,候选疫苗与收费样受体 3 结合,并通过硅学免疫模拟评估了潜在疫苗产生强烈免疫反应的功效:结论:计算分析表明,拟议的多表位疫苗可安全用于人类,并能引起免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
3.70%
发文量
29
审稿时长
8 weeks
期刊介绍: Clin Exp Vaccine Res, the official English journal of the Korean Vaccine Society, is an international, peer reviewed, and open-access journal. It covers all areas related to vaccines and vaccination. Clin Exp Vaccine Res publishes editorials, review articles, special articles, original articles, case reports, brief communications, and correspondences covering a wide range of clinical and experimental subjects including vaccines and vaccination for human and animals against infectious diseases caused by viruses, bacteria, parasites and tumor. The scope of the journal is to disseminate information that may contribute to elaborate vaccine development and vaccination strategies targeting infectious diseases and tumors in human and animals. Relevant topics range from experimental approaches to (pre)clinical trials for the vaccine research based on, but not limited to, basic laboratory, translational, and (pre)clinical investigations, epidemiology of infectious diseases and progression of all aspects in the health related issues. It is published printed and open accessed online issues (https://ecevr.org) two times per year in 31 January and 31 July. Clin Exp Vaccine Res is linked to many international databases and is made freely available to institutions and individuals worldwide
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