Author
Listed:
- Kuan-Ying Arthur Huang
(Chang Gung Memorial Hospital)
- Mei-Feng Chen
(Research Center for Emerging Viral Infections, Chang Gung University
Bone and Joint Research Center, Chang Gung Memorial Hospital)
- Yhu-Chering Huang
(Chang Gung Memorial Hospital)
- Shin-Ru Shih
(Research Center for Emerging Viral Infections, Chang Gung University)
- Cheng-Hsun Chiu
(Chang Gung Memorial Hospital
Molecular Infectious Disease Research Centre, Chang Gung Memorial Hospital)
- Jainn-Jim Lin
(Chang Gung Memorial Hospital)
- Jen-Ren Wang
(College of Medicine, National Cheng Kung University)
- Kuo-Chien Tsao
(Chang Gung Memorial Hospital)
- Tzou-Yien Lin
(Chang Gung Memorial Hospital
Chang Gung University)
Abstract
Protective antibody levels are critical for protection from severe enterovirus 71 infection. However, little is known about the specificities and functional properties of the enterovirus 71-specific antibodies induced by natural infection in humans. Here we characterize 191 plasmablast-derived monoclonal antibodies from three enterovirus 71-infected children, each of whom shows a distinct serological response. Of the 84 enterovirus 71-specific antibodies, neutralizing antibodies that target the rims and floor of the capsid canyon exhibit broad and potent activities at the nanogram level against viruses isolated in 1998–2016. We also find a subset of infected children whose enterovirus 71-specific antibodies are focused on the 3- and 2-fold plateau epitopes localized at the margin of pentamers, and this type of antibody response is associated with lower serum titers against recently circulating strains. Our data provide new insights into the enterovirus 71-specific antibodies induced by natural infection at the serological and clonal levels.
Suggested Citation
Kuan-Ying Arthur Huang & Mei-Feng Chen & Yhu-Chering Huang & Shin-Ru Shih & Cheng-Hsun Chiu & Jainn-Jim Lin & Jen-Ren Wang & Kuo-Chien Tsao & Tzou-Yien Lin, 2017.
"Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children,"
Nature Communications, Nature, vol. 8(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00736-9
DOI: 10.1038/s41467-017-00736-9
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