病毒样颗粒(vlp)是黄病毒疫苗开发的重要工具

L. Castilho, Nathalia R. Mattos, Wallace S. Abreu, M. Gutarra
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引用次数: 1

摘要

黄病毒,如登革热、寨卡病毒、黄热病、西尼罗河病毒和日本脑炎病毒,是属于黄病毒科(黄病毒属)的核糖核酸病毒。它们代表了一个重要的全球健康问题,因为世界上大多数地区至少有一种病毒是地方病。尽管目前存在五种黄病毒的疫苗,但仍需要新的疫苗来保护已建立、新出现和重新出现的黄病毒。过去十年中经历的黄热病疫苗短缺,加上YFV传播到亚洲的风险,以及对某些人群的疫苗接种限制,表明即使有高效疫苗,也可能需要新的和改进的疫苗。病毒样颗粒(VLP)是模仿病毒的多蛋白结构,但不包含病毒的遗传物质。因此,VLP具有良好的免疫原性和高安全性,可以追溯到20世纪80年代第一种重组乙型肝炎疫苗的推出。黄病毒样颗粒(FVLP)已被广泛研究,特别是针对DENV、JEV和ZIKV,并可能产生基于VLP的下一代重组亚单位黄病毒疫苗,该疫苗结合了旨在确保高效性并将感染其他黄病毒时抗体依赖性增强(ADE)的风险降至最低的分子特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Virus-Like Particles (VLPs) as Important Tools for Flavivirus Vaccine Development
Flaviviruses, such as dengue, zika, yellow fever, West Nile, and Japanese encephalitis virus, are RNA viruses belonging to the Flaviviridae family (genus Flavivirus). They represent an important global health concern, since most areas of the world are endemic for at least one of these viruses. Although vaccines for five flaviviruses currently exist, there is a need for new vaccines to protect from established, emerging, and reemerging flaviviruses. Yellow fever vaccine shortages experienced in the last decade, combined with the risk of YFV spread to Asia and the restrictions of vaccine administration to certain population segments, show that even when a highly efficacious vaccine is available, new and improved vaccines might be needed. Virus-like particles (VLPs) are multiprotein structures that mimic the virus, but do not contain its genetic material. As such, VLPs have an excellent track record of strong immunogenicity and high safety, dating back to the introduction of the first recombinant hepatitis B vaccine in the 1980s. Flavivirus-like particles (FVLPs) have been extensively studied, especially for DENV, JEV, and ZIKV, and could give rise to next-generation recombinant subunit flavivirus vaccines based on VLPs incorporating molecular features intended to ensure high efficacy and minimize the risk of antibody-dependent enhancement (ADE) upon infection with other flaviviruses.
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