| Literature DB >> 32027857 |
Maozhou He1, Longfa Xu1, Qingbing Zheng1, Rui Zhu1, Zhichao Yin1, Zhenghui Zha1, Yu Lin1, Lisheng Yang2, Yang Huang1, Xiangzhong Ye2, Shuxuan Li1, Wangheng Hou1, Yangtao Wu1, Jinle Han2, Dongxiao Liu1, Zekai Li1, Zhenqin Chen1, Hai Yu1, Yuqiong Que1, Yingbin Wang1, Xiaodong Yan3, Jun Zhang1, Ying Gu1, Z Hong Zhou4, Tong Cheng5, Shaowei Li6, Ningshao Xia7.
Abstract
Hand, foot, and mouth disease is a common childhood illness primarily caused by coxsackievirus A16 (CVA16), for which there are no current vaccines or treatments. We identify three CVA16-specific neutralizing monoclonal antibodies (nAbs) with therapeutic potential: 18A7, 14B10, and NA9D7. We present atomic structures of these nAbs bound to all three viral particle forms-the mature virion, A-particle, and empty particle-and show that each Fab can simultaneously occupy the mature virion. Additionally, 14B10 or NA9D7 provide 100% protection against lethal CVA16 infection in a neonatal mouse model. 18A7 binds to a non-conserved epitope present in all three particles, whereas 14B10 and NA9D7 recognize broad protective epitopes but only bind the mature virion. NA9D7 targets an immunodominant site, which may overlap the receptor-binding site. These findings indicate that CVA16 vaccines should be based on mature virions and that these antibodies could be used to discriminate optimal virion-based immunogens.Entities:
Keywords: coxsackievirus A16; cryo-EM structure; therapeutic antibody; vaccine design
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Year: 2020 PMID: 32027857 PMCID: PMC7539366 DOI: 10.1016/j.chom.2020.01.003
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023