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新型肠道病毒71型疫苗的研发

Development of Novel Vaccines against Enterovirus-71.

作者信息

Yee Pinn Tsin Isabel, Poh Chit Laa

机构信息

Virology Research Group, Vice Chancellor's Office, Sunway University, Bandar Sunway, Kuala Lumpur, Selangor 47500, Malaysia.

出版信息

Viruses. 2015 Dec 30;8(1):1. doi: 10.3390/v8010001.

DOI:10.3390/v8010001
PMID:26729152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4728561/
Abstract

The hand, foot and mouth disease is caused by a group of Enteroviruses such as Enterovirus 71 (EV-A71) and Coxsackievirus CV-A5, CV-A8, and CV-A16. Mild symptoms of EV-A71 infection in children range from high fever, vomiting, rashes and ulcers in mouth but can produce more severe symptoms such as brainstem and cerebellar encephalitis, leading up to cardiopulmonary failure and death. The lack of vaccines and antiviral drugs against EV-A71 highlights the urgency of developing preventive and treatment agents against EV-A71 to prevent further fatalities. Research groups have developed experimental inactivated vaccines, recombinant Viral Protein 1 (VP1) vaccine and virus-like particles (VLPs). The inactivated EV-A71 vaccine is considered the safest viral vaccine, as there will be no reversion to the infectious wild type strain. The recombinant VP1 vaccine is a cost-effective immunogen, while VLPs contain an arrangement of epitopes that can elicit neutralizing antibodies against the virus. As each type of vaccine has its advantages and disadvantages, increased studies are required in the development of such vaccines, whereby high efficacy, long-lasting immunity, minimal risk to those vaccinated, safe and easy production, low cost, dispensing the need for refrigeration and convenient delivery are the major goals in their design.

摘要

手足口病由一组肠道病毒引起,如肠道病毒71型(EV - A71)以及柯萨奇病毒CV - A5、CV - A8和CV - A16。儿童感染EV - A71的轻微症状包括高烧、呕吐、皮疹和口腔溃疡,但也可能产生更严重的症状,如脑干和小脑脑炎,甚至导致心肺衰竭和死亡。缺乏针对EV - A71的疫苗和抗病毒药物凸显了开发针对EV - A71的预防和治疗药物以防止更多死亡的紧迫性。研究团队已经开发出了实验性灭活疫苗、重组病毒蛋白1(VP1)疫苗和病毒样颗粒(VLP)。灭活的EV - A71疫苗被认为是最安全的病毒疫苗,因为不会回复到具有传染性的野生型毒株。重组VP1疫苗是一种具有成本效益的免疫原,而VLP包含能引发针对该病毒的中和抗体的表位排列。由于每种疫苗都有其优缺点,因此在这类疫苗的开发中需要进行更多研究,高效、持久免疫、对接种者风险最小、安全易生产、低成本、无需冷藏和便于分发是其设计的主要目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/186f/4728561/81ba299cc272/viruses-08-00001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/186f/4728561/576a82299e74/viruses-08-00001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/186f/4728561/81ba299cc272/viruses-08-00001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/186f/4728561/576a82299e74/viruses-08-00001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/186f/4728561/81ba299cc272/viruses-08-00001-g002.jpg

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EV71 vaccines: a milestone in the history of global vaccine development.
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Microbiol Spectr. 2023 Jun 15;11(3):e0535222. doi: 10.1128/spectrum.05352-22. Epub 2023 May 25.
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Virus-CKB 2.0: Viral-Associated Disease-Specific Chemogenomics Knowledgebase.病毒-慢性肾脏病2.0:病毒相关疾病特异性化学基因组学知识库
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A novel rat CVB1-VP1 monoclonal antibody 3A6 detects a broad range of enteroviruses.一种新型大鼠 CVB1-VP1 单克隆抗体 3A6 可检测广泛的肠道病毒。
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