Uniformed Services University, Bethesda, MD, 20814, USA.
National Eye Institute, National Institutes of Health, Bethesda, MD, USA.
Sci Rep. 2017 Sep 5;7(1):10498. doi: 10.1038/s41598-017-10901-1.
Structural and functional homologies between the Zika and Dengue viruses' envelope proteins raise the possibility that cross-reactive antibodies induced following Zika virus infection might enhance subsequent Dengue infection. Using the rhesus macaque model we show that prior infection with Zika virus leads to a significant enhancement of Dengue-2 viremia that is accompanied by neutropenia, lympocytosis, hyperglycemia, and higher reticulocyte counts, along with the activation of pro-inflammatory monocyte subsets and release of inflammatory mediators. Zika virus infection induced detectable Dengue cross-reactive serum IgG responses that significantly amplified after Dengue-2 virus infection. Serum from Zika virus immune animals collected prior to Dengue-2 infection showed significant capacity for in vitro antibody dependent enhancement of Dengue-1, 2, 3 and 4 serotypes suggesting that pre-existing immunity to Zika virus could potentially enhance infection by heterologous Dengue serotypes. Our results provide first in vivo evidence that prior exposure to Zika virus infection can enhance Dengue infection, which has implications for understanding pathogenesis and the development of vaccines.
寨卡病毒和登革热病毒包膜蛋白之间的结构和功能同源性提出了一种可能性,即寨卡病毒感染后诱导的交叉反应性抗体可能增强随后的登革热感染。我们使用恒河猴模型表明,寨卡病毒感染前会导致登革热 2 型病毒血症显著增强,同时伴有中性粒细胞减少、淋巴细胞增多、高血糖和网织红细胞计数升高,以及促炎单核细胞亚群的激活和炎症介质的释放。寨卡病毒感染诱导可检测到的登革热交叉反应性血清 IgG 反应,在登革热 2 型病毒感染后显著增强。在登革热 2 型病毒感染前采集的寨卡病毒免疫动物血清显示出对体外抗体依赖性增强登革热 1、2、3 和 4 血清型的显著能力,这表明对寨卡病毒的预先存在的免疫力可能会增强对异源登革热血清型的感染。我们的研究结果首次提供了体内证据,表明先前接触寨卡病毒感染可以增强登革热感染,这对理解发病机制和疫苗开发具有重要意义。