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Quantitative evaluation of protective antibody response induced by hepatitis E vaccine in humans

Gui-Ping Wen, Linling He, Zi-Min Tang, Si-Ling Wang, Xu Zhang, Yuan-Zhi Chen, Xiaohe Lin, Chang Liu, Jia-Xin Chen, Dong Ying, Zi-Hao Chen, Ying-Bin Wang, Wen-Xin Luo, Shou-Jie Huang, Shao-Wei Li, Jun Zhang, Zi-Zheng Zheng (), Jiang Zhu () and Ning-Shao Xia ()
Additional contact information
Gui-Ping Wen: Xiamen University
Linling He: The Scripps Research Institute
Zi-Min Tang: Xiamen University
Si-Ling Wang: Xiamen University
Xu Zhang: Xiamen University
Yuan-Zhi Chen: Xiamen University
Xiaohe Lin: The Scripps Research Institute
Chang Liu: Xiamen University
Jia-Xin Chen: Xiamen University
Dong Ying: Xiamen University
Zi-Hao Chen: Xiamen University
Ying-Bin Wang: Xiamen University
Wen-Xin Luo: Xiamen University
Shou-Jie Huang: Xiamen University
Shao-Wei Li: Xiamen University
Jun Zhang: Xiamen University
Zi-Zheng Zheng: Xiamen University
Jiang Zhu: The Scripps Research Institute
Ning-Shao Xia: Xiamen University

Nature Communications, 2020, vol. 11, issue 1, 1-13

Abstract: Abstract Efficacy evaluation through human trials is crucial for advancing a vaccine candidate to clinics. Next-generation sequencing (NGS) can be used to quantify B cell repertoire response and trace antibody lineages during vaccination. Here, we demonstrate this application with a case study of Hecolin®, the licensed vaccine for hepatitis E virus (HEV). Four subjects are administered the vaccine following a standard three-dose schedule. Vaccine-induced antibodies exhibit a high degree of clonal diversity, recognize five conformational antigenic sites of the genotype 1 HEV p239 antigen, and cross-react with other genotypes. Unbiased repertoire sequencing is performed for seven time points over six months of vaccination, with maturation pathways characterize for a set of vaccine-induced antibodies. In addition to dynamic repertoire profiles, NGS analysis reveals differential patterns of HEV-specific antibody lineages and highlights the necessity of the long vaccine boost. Together, our study presents a quantitative strategy for vaccine evaluation in small-scale human studies.

Date: 2020
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DOI: 10.1038/s41467-020-17737-w

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