Department of Biomedical Sciences, University of North Dakota, School of Medicine and Health Sciences, Grand Forks, ND, 58202, USA.
Division of Infectious Diseases and Vaccinology, School of Public Health, University of California Berkeley, Berkeley, CA, 94720, USA.
Antiviral Res. 2020 Nov;183:104923. doi: 10.1016/j.antiviral.2020.104923. Epub 2020 Sep 23.
Dengue is the most prevalent arboviral disease in humans and a continually increasing global public health burden. To date, there are no approved antiviral therapies against dengue virus (DENV) and the only licensed vaccine, Dengvaxia, is exclusively indicated for individuals with prior DENV infection. Endothelial hyperpermeability and vascular leak, pathogenic hallmarks of severe dengue disease, can be directly triggered by DENV non-structural protein 1 (NS1). As such, anti-NS1 antibodies can prevent NS1-triggered endothelial dysfunction in vitro and pathogenesis in vivo. Recently, goose-derived anti-DENV immunoglobulin Y (IgY) antibodies were shown to neutralize DENV and Zika virus (ZIKV) infection without adverse effects, such as antibody-dependent enhancement (ADE). In this study, we used egg yolks from DENV-immunized geese to purify IgY antibodies specific to DENV NS1 epitopes. We determined that 2 anti-NS1 IgY antibodies, NS1-1 and NS1-8, were capable of neutralizing DENV infection in vitro. In addition, these antibodies did not cross-react with the DENV Envelope (E) protein nor enhance DENV or ZIKV infection in vitro. Intriguingly, NS1-8, but not NS1-1, partially blocked NS1-induced endothelial dysfunction in vitro while neither antibody blocked binding of soluble NS1 to cells. Finally, prophylactic treatment of mice with NS1-8 conferred significant protection against lethal DENV challenge. Although further research is needed to define the mechanism of action of these antibodies, our findings highlight the potential of anti-NS1 IgY as a promising prophylactic approach against DENV infection.
登革热是人类中最普遍的虫媒病毒病,也是一个持续增加的全球公共卫生负担。迄今为止,还没有针对登革病毒(DENV)的批准的抗病毒疗法,唯一获得许可的疫苗 Dengvaxia 仅适用于先前感染过 DENV 的个体。内皮细胞通透性增加和血管渗漏是重症登革热疾病的病理特征,可以被 DENV 非结构蛋白 1(NS1)直接触发。因此,抗 NS1 抗体可以预防 NS1 在体外触发的内皮功能障碍和体内发病机制。最近,研究表明,鹅源性抗登革病毒免疫球蛋白 Y(IgY)抗体可以中和登革热病毒和寨卡病毒(ZIKV)感染,而没有不良反应,如抗体依赖性增强(ADE)。在这项研究中,我们使用来自 DENV 免疫鹅的蛋黄来纯化针对 DENV NS1 表位的 IgY 抗体。我们确定了 2 种抗 NS1 IgY 抗体,NS1-1 和 NS1-8,能够在体外中和 DENV 感染。此外,这些抗体不会与 DENV 包膜(E)蛋白发生交叉反应,也不会在体外增强 DENV 或 ZIKV 感染。有趣的是,NS1-8 而不是 NS1-1,部分阻断了 NS1 在体外诱导的内皮功能障碍,而这两种抗体都不能阻断可溶性 NS1 与细胞的结合。最后,用 NS1-8 对小鼠进行预防性治疗可显著预防致死性 DENV 攻击。尽管还需要进一步研究来确定这些抗体的作用机制,但我们的研究结果强调了抗 NS1 IgY 作为预防 DENV 感染的一种有前途的方法的潜力。