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Discovery and structural characterization of a therapeutic antibody against coxsackievirus A10.

Rui ZhuLongfa XuQingbing ZhengYanxiang CuiShao-Wei LiMaozhou HeZhichao YinDongxiao LiuShuxuan LiZizhen LiZhenqin ChenHai YuYuqiong QueChe LiuZhibo KongJun ZhangTimothy S BakerXiaodong YanZ Hong ZhouTong ChengNing-Shao Xia
Published in: Science advances (2018)
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.
Keyphrases
  • electron microscopy
  • public health
  • high resolution
  • genome wide
  • metabolic syndrome
  • adipose tissue
  • single cell
  • zika virus
  • high fat diet induced