Linear B-cell epitopes on Zika virus´s envelope protein: a rational approach to determination of highly specific targets against Zika virus

Rodrigo Silva, F. Conte, S. Fontes, P. C. Neves, J. C. Sánchez-Arcila, L. Pinto
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引用次数: 1

Abstract

Introduction: Zika virus (ZIKV) is an arbovirus and belongs to the Flaviviridae family, like the related dengue, yellow fever, West Nile, and Japanese encephalitis viruses. Although ZIKV usually causes an asymptomatic or mildly symptomatic disease in infected adults, it can lead to severe brain abnormalities in fetuses, who are infected in utero by vertical transmission of the virus through the placenta, and is associated with serious neurological complications such Guillain-Barre syndrome and meningoencephalitis. Despite this, there are no specific treatments or vaccines against ZIKV. On this context, considering that the Envelope protein of Flavivirus is essential to invasion of host cells and is the major target of neutralizing antibodies, the identification of its immunogenic regions is a crucial step to the development of immunotherapies based on monoclonal antibodies and novel vaccines.
寨卡病毒包膜蛋白上的线性b细胞表位:一种确定寨卡病毒高度特异性靶点的合理方法
寨卡病毒(ZIKV)是一种虫媒病毒,与相关的登革热、黄热病、西尼罗河病毒和日本脑炎病毒一样,属于黄病毒科。虽然寨卡病毒通常在受感染的成年人中引起无症状或轻度症状的疾病,但它可导致胎儿严重的脑部异常,胎儿在子宫内通过胎盘垂直传播病毒而受到感染,并与格林-巴利综合征和脑膜脑炎等严重神经系统并发症有关。尽管如此,目前还没有针对寨卡病毒的特定治疗方法或疫苗。在此背景下,考虑到黄病毒的包膜蛋白是入侵宿主细胞所必需的,也是中和抗体的主要靶点,鉴定其免疫原区是开发基于单克隆抗体和新型疫苗的免疫疗法的关键一步。
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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