衣壳
柯萨奇病毒
抗体
分离(微生物学)
病毒学
效力
计算生物学
中和抗体
免疫学
生物
微生物学
肠道病毒
病毒
体外
生物化学
作者
Rui Zhu,Longfa Xu,Qingbing Zheng,Yanxiang Cui,Shaowei Li,Shaowei Li,Maozhou He,Zhichao Yin,Dongxiao Liu,Shuxuan Li,Shuxuan Li,Zizhen Li,Zhenqin Chen,Hai Yu,Yuqiong Que,Che Liu,Zhibo Kong,Jun Zhang,Timothy S. Baker,Xiaodong Yan
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2018-09-07
卷期号:4 (9): eaat7459-eaat7459
被引量:28
标识
DOI:10.1126/sciadv.aat7459
摘要
Coxsackievirus A10 (CVA10) recently emerged as a major pathogen of hand, foot, and mouth disease and herpangina in children worldwide, and lack of a vaccine or a cure against CVA10 infections has made therapeutic antibody identification a public health priority. By targeting a local isolate, CVA10-FJ-01, we obtained a potent antibody, 2G8, against all three capsid forms of CVA10. We show that 2G8 exhibited both 100% preventive and 100% therapeutic efficacy against CVA10 infection in mice. Comparisons of the near-atomic cryo-electron microscopy structures of the three forms of CVA10 capsid and their complexes with 2G8 Fab reveal that a single Fab binds a border region across the three capsid proteins (VP1 to VP3) and explain 2G8's remarkable cross-reactivities against all three capsid forms. The atomic structures of this first neutralizing antibody of CVA10 should inform strategies for designing vaccines and therapeutics against CVA10 infections.
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