A Bibliometric Analysis on Multi-epitope Vaccine Development Against SARS-CoV-2: Current Status, Development, and Future Directions.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kanwal Khalid, Fiaz Ahmad, Ayaz Anwar, Seng-Kai Ong
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Abstract

The etiological agent for the coronavirus disease 2019 (COVID-19), the SARS-CoV-2, caused a global pandemic. Although mRNA, viral-vectored, DNA, and recombinant protein vaccine candidates were effective against the SARS-CoV-2 Wuhan strain, the emergence of SARS-CoV-2 variants of concern (VOCs) reduced the protective efficacies of these vaccines. This necessitates the need for effective and accelerated vaccine development against mutated VOCs. The development of multi-epitope vaccines against SARS-CoV-2 based on in silico identification of highly conserved and immunogenic epitopes is a promising strategy for future SARS-CoV-2 vaccine development. Considering the evolving landscape of the COVID-19 pandemic, we have conducted a bibliometric analysis to consolidate current findings and research trends in multi-epitope vaccine development to provide insights for future vaccine development strategies. Analysis of 102 publications on multi-epitope vaccine development against SARS-CoV-2 revealed significant growth and global collaboration, with India leading in the number of publications, along with an identification of the most prolific authors. Key journals included the Journal of Biomolecular Structure and Dynamics, while top collaborations involved Pakistan-China and India-USA. Keyword analysis showed a prominent focus on immunoinformatics, epitope prediction, and spike glycoprotein. Advances in immunoinformatics, including AI-driven epitope prediction, offer promising avenues for the development of safe and effective multi-epitope vaccines. Immunogenicity may be further improved through nanoparticle-based systems or the use of adjuvants along with real-time genomic surveillance to tailor vaccines against emerging variants.

SARS-CoV-2多表位疫苗研制的文献计量学分析:现状、发展与未来方向
2019冠状病毒病(COVID-19)的病原SARS-CoV-2引起了全球大流行。虽然mRNA、病毒载体、DNA和重组蛋白候选疫苗对SARS-CoV-2武汉株有效,但SARS-CoV-2关注变异体(VOCs)的出现降低了这些疫苗的保护效果。这就需要有效和加速开发针对突变挥发性有机化合物的疫苗。基于高度保守和免疫原性抗原表位的计算机鉴定开发多表位疫苗是未来SARS-CoV-2疫苗开发的一个有前景的策略。考虑到COVID-19大流行的不断变化的格局,我们进行了文献计量分析,以整合多表位疫苗开发的当前发现和研究趋势,为未来的疫苗开发策略提供见解。对102份关于SARS-CoV-2多表位疫苗开发的出版物的分析显示,全球合作显著增长,其中印度在出版物数量方面领先,并确定了最多产的作者。重点期刊包括《生物分子结构与动力学杂志》,而顶级合作涉及巴基斯坦-中国和印度-美国。关键词分析显示免疫信息学、表位预测和刺突糖蛋白是重点。免疫信息学的进步,包括人工智能驱动的表位预测,为开发安全有效的多表位疫苗提供了有希望的途径。免疫原性可以通过基于纳米颗粒的系统或使用佐剂以及实时基因组监测来进一步改善,以定制针对新出现变体的疫苗。
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
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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