Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
California National Primate Research Center, University of California, Davis, Davis, CA 95616, USA; Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, CA 95616, USA.
Cell Rep. 2018 Nov 6;25(6):1385-1394.e7. doi: 10.1016/j.celrep.2018.10.031.
Zika virus (ZIKV) causes severe neurologic complications and fetal aberrations. Vaccine development is hindered by potential safety concerns due to antibody cross-reactivity with dengue virus and the possibility of disease enhancement. In contrast, passive administration of anti-ZIKV antibodies engineered to prevent enhancement may be safe and effective. Here, we report on human monoclonal antibody Z021, a potent neutralizer that recognizes an epitope on the lateral ridge of the envelope domain III (EDIII) of ZIKV and is protective against ZIKV in mice. When administered to macaques undergoing a high-dose ZIKV challenge, a single anti-EDIII antibody selected for resistant variants. Co-administration of two antibodies, Z004 and Z021, which target distinct sites on EDIII, was associated with a delay and a 3- to 4-log decrease in peak viremia. Moreover, the combination of these antibodies engineered to avoid enhancement prevented viral escape due to mutation in macaques, a natural host for ZIKV.
寨卡病毒(ZIKV)可引起严重的神经并发症和胎儿畸形。由于抗体与登革热病毒的交叉反应以及疾病加重的可能性,疫苗的开发受到潜在安全问题的阻碍。相比之下,通过被动给予旨在预防增强作用的抗 ZIKV 抗体,可能是安全有效的。在这里,我们报告了人源单克隆抗体 Z021,它是一种有效的中和抗体,可识别 ZIKV 包膜域 III(EDIII)侧脊上的表位,并且对小鼠中的 ZIKV 具有保护作用。当给予在高剂量 ZIKV 挑战下的猕猴时,选择对耐药变体具有抗性的单一抗 EDIII 抗体。两种抗体(Z004 和 Z021)联合使用,靶向 EDIII 上的不同位点,与病毒血症峰值的延迟和 3 到 4 个对数减少相关。此外,为避免增强作用而设计的这些抗体的组合可防止由于猕猴(ZIKV 的天然宿主)中的突变而导致的病毒逃逸。