Graham Stephen D, Tu Huy A, McElvany Benjamin D, Graham Nancy R, Grinyo Ariadna, Davidson Edgar, Doranz Benjamin J, Diehl Sean A, de Silva Aravinda M, Markmann Alena Janda
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Department of Microbiology and Molecular Genetics, Vaccine Testing Center, Cellular, Molecular, and Biomedical Sciences Program, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.
J Virol. 2021 Apr 12;95(9). doi: 10.1128/JVI.02423-20.
Zika virus (ZIKV), a mosquito-transmitted flavivirus, caused a large epidemic in Latin America between 2015 and 2017. Effective ZIKV vaccines and treatments are urgently needed to prevent future epidemics and severe disease sequelae. People infected with ZIKV develop strongly neutralizing antibodies linked to viral clearance and durable protective immunity. To understand the mechanisms of protective immunity and to support the development of ZIKV vaccines, we characterize here a strongly neutralizing antibody, B11F, isolated from a patient who recovered from ZIKV. Our results indicate that B11F targets a complex epitope on the virus that spans domains I and III of the envelope glycoprotein. While previous studies point to quaternary epitopes centered on domain II of the ZIKV E glycoprotein as targets of strongly neutralizing and protective human antibodies, we uncover a new site spanning domains I and III as a target of strongly neutralizing human antibodies. People infected with Zika virus develop durable neutralizing antibodies that prevent repeat infections. In the current study, we characterize a ZIKV-neutralizing human monoclonal antibody isolated from a patient after recovery. Our studies establish a novel site on the viral envelope that is targeted by human neutralizing antibodies. Our results are relevant to understanding how antibodies block infection and to guiding the design and evaluation of candidate vaccines.
寨卡病毒(ZIKV)是一种通过蚊子传播的黄病毒,在2015年至2017年间在拉丁美洲引发了大规模疫情。迫切需要有效的寨卡病毒疫苗和治疗方法来预防未来的疫情和严重的疾病后遗症。感染寨卡病毒的人会产生与病毒清除和持久保护性免疫相关的强效中和抗体。为了了解保护性免疫的机制并支持寨卡病毒疫苗的开发,我们在此对一种从寨卡病毒康复患者体内分离出的强效中和抗体B11F进行了表征。我们的结果表明,B11F靶向病毒上一个跨越包膜糖蛋白结构域I和III的复杂表位。虽然先前的研究指出,以寨卡病毒E糖蛋白结构域II为中心的四级表位是强效中和及保护性人类抗体的靶点,但我们发现了一个跨越结构域I和III的新位点作为强效中和人类抗体的靶点。感染寨卡病毒的人会产生持久的中和抗体,从而预防再次感染。在本研究中,我们对一名康复后患者体内分离出的寨卡病毒中和人单克隆抗体进行了表征。我们的研究在病毒包膜上确定了一个新的人类中和抗体靶向位点。我们的结果对于理解抗体如何阻断感染以及指导候选疫苗的设计和评估具有重要意义。