Elliott Kenneth C, Mattapallil Joseph J
Department of Microbiology & Immunology, The Henry M Jackson Foundation for Military Medicine, Uniformed Services University, Bethesda, MD 20814, USA.
Department of Microbiology & Immunology, Uniformed Services University, Bethesda, MD 20814, USA.
Pathogens. 2024 Feb 15;13(2):177. doi: 10.3390/pathogens13020177.
Zika virus (ZIKV) is a reemerging flavivirus that is primarily spread through bites from infected mosquitos. It was first discovered in 1947 in sentinel monkeys in Uganda and has since been the cause of several outbreaks, primarily in tropical and subtropical areas. Unlike earlier outbreaks, the 2015-2016 epidemic in Brazil was characterized by the emergence of neurovirulent strains of ZIKV strains that could be sexually and perinatally transmitted, leading to the Congenital Zika Syndrome (CZS) in newborns, and Guillain-Barre Syndrome (GBS) along with encephalitis and meningitis in adults. The immune response elicited by ZIKV infection is highly effective and characterized by the induction of both ZIKV-specific neutralizing antibodies and robust effector CD8 T cell responses. However, the structural similarities between ZIKV and Dengue virus (DENV) lead to the induction of cross-reactive immune responses that could potentially enhance subsequent DENV infection, which imposes a constraint on the development of a highly efficacious ZIKV vaccine. The isolation and characterization of antibodies capable of cross-neutralizing both ZIKV and DENV along with cross-reactive CD8 T cell responses suggest that vaccine immunogens can be designed to overcome these constraints. Here we review the structural characteristics of ZIKV along with the evidence of neuropathogenesis associated with ZIKV infection and the complex nature of the immune response that is elicited by ZIKV infection.
寨卡病毒(ZIKV)是一种再度出现的黄病毒,主要通过受感染蚊子的叮咬传播。它于1947年在乌干达的哨兵猴中首次被发现,此后一直是几次疫情爆发的原因,主要发生在热带和亚热带地区。与早期疫情不同,2015 - 2016年巴西的疫情特点是出现了具有神经毒性的寨卡病毒毒株,这些毒株可通过性传播和母婴传播,导致新生儿出现先天性寨卡综合征(CZS),并在成人中引发格林 - 巴利综合征(GBS)以及脑炎和脑膜炎。寨卡病毒感染引发的免疫反应非常有效,其特征是诱导产生寨卡病毒特异性中和抗体以及强大的效应性CD8 T细胞反应。然而,寨卡病毒与登革病毒(DENV)之间的结构相似性导致产生交叉反应性免疫反应,这可能会潜在地增强随后的登革病毒感染,这对开发高效的寨卡病毒疫苗构成了限制。能够交叉中和寨卡病毒和登革病毒的抗体的分离和特性以及交叉反应性CD8 T细胞反应表明,可以设计疫苗免疫原以克服这些限制。在此,我们综述寨卡病毒的结构特征,以及与寨卡病毒感染相关的神经发病机制的证据,以及寨卡病毒感染引发的免疫反应的复杂性质。