CAS Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Virol Sin. 2019 Apr;34(2):168-174. doi: 10.1007/s12250-019-00093-5. Epub 2019 Apr 24.
As we know more about Zika virus (ZIKV), as well as its linkage to birth defects (microcephaly) and autoimmune neurological syndromes, we realize the importance of developing an efficient vaccine against it. Zika virus disease has affected many countries and is becoming a major public health concern. To deal with the infection of ZIKV, plenty of experiments have been done on selection of neutralizing antibodies that can target the envelope (E) protein on the surface of the virion. However, the existence of antibody-dependent enhancement (ADE) effect might limit the use of them as therapeutic candidates. In this review, we classify the neutralizing antibodies against ZIKV based on the epitopes and summarize the resolved structural information on antibody/antigen complex from X-ray crystallography and cryo-electron microscopy (cryo-EM), which might be useful for further development of potent neutralizing antibodies and vaccines toward clinical use.
随着我们对寨卡病毒(ZIKV)及其与出生缺陷(小头畸形)和自身免疫性神经系统综合征的联系有了更多的了解,我们意识到开发针对它的有效疫苗的重要性。寨卡病毒病已经影响了许多国家,正在成为一个主要的公共卫生关注点。为了应对 ZIKV 的感染,已经进行了大量的实验来选择能够针对病毒表面包膜(E)蛋白的中和抗体。然而,抗体依赖性增强(ADE)效应的存在可能限制了它们作为治疗候选物的使用。在这篇综述中,我们根据表位对寨卡病毒的中和抗体进行分类,并总结了 X 射线晶体学和低温电子显微镜(cryo-EM)解析的抗体/抗原复合物的结构信息,这可能对进一步开发针对临床应用的有效中和抗体和疫苗有用。