Sun Jin, Du Senyan, Zheng Zhihang, Cheng Gong, Jin Xia
Viral Disease and Vaccine Translational Research Unit, CAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China.
Tsinghua-Peking Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, China.
Front Microbiol. 2020 Mar 20;11:362. doi: 10.3389/fmicb.2020.00362. eCollection 2020.
Dengue virus (DENV) and Zika virus (ZIKV) are two mosquito-borne flaviviruses afflicting nearly half of the world population. Human infection by these viruses can either be asymptomatic or manifest as clinical diseases from mild to severe. Despite more cases are presented as self-limiting febrile illness, severe dengue disease can be manifested as hemorrhagic fever and hemorrhagic shock syndrome, and ZIKV infection has been linked to increased incidence of peripheral neuropathy Guillain-Barre syndrome and central neural disease such as microcephaly. The current prevention and treatment of these infectious diseases are either non-satisfactory or entirely lacking. Because DENV and ZIKV have much similarities in genomic and structural features, almost identical mode of mosquito-mediated transmission, and probably the same pattern of host innate and adaptive immunity toward them, it is reasonable and often desirable to investigate these two viruses side-by-side, and thereby devise common countermeasures against both. Here, we review the existing knowledge on DENV and ZIKV regarding epidemiology, molecular virology, protective immunity and vaccine development, discuss recent new discoveries on the functions of flavivirus NS1 protein in viral pathogenesis and transmission, and propose a one-two punch strategy using vaccine and vector blockade to overcome antibody-dependent enhancement and defeat Dengue and Zika viruses.
登革病毒(DENV)和寨卡病毒(ZIKV)是两种由蚊子传播的黄病毒,困扰着世界近一半的人口。人类感染这些病毒后可能没有症状,也可能表现为从轻度到重度的临床疾病。尽管更多的病例表现为自限性发热疾病,但严重的登革热疾病可表现为出血热和出血性休克综合征,而寨卡病毒感染与周围神经病变吉兰-巴雷综合征和中枢神经疾病如小头畸形的发病率增加有关。目前对这些传染病的预防和治疗要么不尽人意,要么完全缺乏。由于登革病毒和寨卡病毒在基因组和结构特征上有很多相似之处,蚊子介导的传播模式几乎相同,而且宿主对它们的固有免疫和适应性免疫模式可能也相同,因此将这两种病毒放在一起研究,并由此制定针对两者的共同对策是合理且常被期望的。在此,我们综述了关于登革病毒和寨卡病毒在流行病学、分子病毒学、保护性免疫和疫苗开发方面的现有知识,讨论了黄病毒NS1蛋白在病毒发病机制和传播中的功能的最新新发现,并提出了一种使用疫苗和阻断载体的双重打击策略,以克服抗体依赖性增强并战胜登革病毒和寨卡病毒。