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Discovery and structural characterization of a therapeutic antibody against coxsackievirus A10

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-F...

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Detalles Bibliográficos
Autores principales: Zhu, Rui, Xu, Longfa, Zheng, Qingbing, Cui, Yanxiang, Li, Shaowei, He, Maozhou, Yin, Zhichao, Liu, Dongxiao, Li, Shuxuan, Li, Zizhen, Chen, Zhenqin, Yu, Hai, Que, Yuqiong, Liu, Che, Kong, Zhibo, Zhang, Jun, Baker, Timothy S., Yan, Xiaodong, Hong Zhou, Z., Cheng, Tong, Xia, Ningshao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155056/
https://www.ncbi.nlm.nih.gov/pubmed/30255146
http://dx.doi.org/10.1126/sciadv.aat7459
Descripción
Sumario: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.