J
Jianbo Wu
Researcher at Fudan University
Publications - 10
Citations - 229
Jianbo Wu is an academic researcher from Fudan University. The author has contributed to research in topics: Antibody & Biology. The author has an hindex of 3, co-authored 5 publications receiving 54 citations. Previous affiliations of Jianbo Wu include Fudan University Shanghai Medical College.
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Journal ArticleDOI
Enhancement versus neutralization by SARS-CoV-2 antibodies from a convalescent donor associates with distinct epitopes on the RBD.
Yunjiao Zhou,Zezhong Liu,Shibo Li,Wei Xu,Qianqian Zhang,Israel Tojal da Silva,Cheng Li,Yanling Wu,Qingling Jiang,Zhenmi Liu,Qiujing Wang,Yu Guo,Jianbo Wu,Chengjian Gu,Xia Cai,Di Qu,Christian T. Mayer,Xiangxi Wang,Shibo Jiang,Tianlei Ying,Zhenghong Yuan,Youhua Xie,Yu-Mei Wen,Lu Lu,Qiao Wang +24 more
TL;DR: In this paper, a convalescent individual with potent IgG neutralizing activity and characterize his antibody response was selected, and the relationship between enhancing versus neutralizing activities and antibody epitopes remains unknown.
Journal ArticleDOI
A Combination of Human Broadly Neutralizing Antibodies against Hepatitis B Virus HBsAg with Distinct Epitopes Suppresses Escape Mutations.
Qiao Wang,Eleftherios Michailidis,Yingpu Yu,Zijun Wang,Arlene Hurley,Deena A. Oren,Christian T. Mayer,Anna Gazumyan,Zhenmi Liu,Yunjiao Zhou,Till Schoofs,Kai-Hui Yao,Jan P. Nieke,Jianbo Wu,Qingling Jiang,Chenhui Zou,Chenhui Zou,Mohanmmad Kabbani,Corrine Quirk,Thiago Y. Oliveira,Kalsang Chhosphel,Qianqian Zhang,William M. Schneider,Cyprien Jahan,Tianlei Ying,Jill Horowitz,Marina Caskey,Mila Jankovic,Davide F. Robbiani,Yumei Wen,Ype P. de Jong,Ype P. de Jong,Charles M. Rice,Michel C. Nussenzweig,Michel C. Nussenzweig +34 more
TL;DR: The co-crystal structure of one of the bNAbs with an HBsAg peptide epitope revealed a stabilized hairpin loop, which contains residues frequently mutated in clinical immune escape variants, provides a molecular explanation for why immunotherapy for HBV infection may require combinations of complementary bNABS.
Posted ContentDOI
A third dose of inactivated vaccine augments the potency, breadth, and duration of anamnestic responses against SARS-CoV-2
Kang Wang,Yunlong Richard Cao,Yunjiao Zhou,Jiajing Wu,Zijing Jia,Yaling Hu,Ayijiang Yisimayi,Wangjun Fu,Lei Wang,Pan Liu,Kaiyue Fan,Ruihong Chen,Lin Wang,Li Jing,Yao Wang,Xiaoqi Ge,Qianqian Zhang,Jianbo Wu,Nan Wang,Wei Wu,Yidan Gao,Jingyun Miao,Yinan Jiang,Lili Qin,Ling Zhu,Weijin Huang,Yanjun Zhang,Huan Zhang,Baisheng Li,Qiang Gao,Xiaoliang Sunney Xie,Youchun Wang,Qiao Wang,Xiangxi Wang +33 more
TL;DR: In this article, the authors dissected the immunogenic profiles of antibodies from 3-dose vaccine, 2-dose and convalescents and found that a third booster dose of inactivated vaccine produces a highly sifted humoral immune response via a sustained evolution of antibodies capable of effectively neutralizing SARS-CoV-2 variants of concern.
Journal ArticleDOI
An ultrapotent pan-β-coronavirus lineage B (β-CoV-B) neutralizing antibody locks the receptor-binding domain in closed conformation by targeting its conserved epitope.
Zezhong Liu,Wei Xu,Zhenguo Chen,Wangjun Fu,Wuqiang Zhan,Yidan Gao,Jie Zhou,Yunjiao Zhou,Jianbo Wu,Qian Wang,Xiang Zhang,Aihua Hao,Wei Wu,Qianqian Zhang,Yaming Li,Kaiyue Fan,Ruihong Chen,Qiaochu Jiang,Christian T. Mayer,Till Schoofs,Youhua Xie,Shibo Jiang,Yu-Mei Wen,Zhenghong Yuan,Kang Wang,Lu Lu,Lei Sun,Qiao Wang +27 more
TL;DR: This article identified a receptor-binding domain (RBD)-binding antibody, XG014, which potently neutralizes β-coronavirus lineage B (β-CoV-B), including SARS-Cov-2, its circulating variants, SARS CoV and bat SARSr CoV WIV1.
Journal ArticleDOI
Selection and structural bases of potent broadly neutralizing antibodies from 3-dose vaccinees that are highly effective against diverse SARS-CoV-2 variants, including Omicron sublineages
Lei Wang,Wangjun Fu,Linlin Bao,Zijing Jia,YuXia Zhang,Yunjiao Zhou,Wei Wu,Jianbo Wu,Qianqian Zhang,Yidan Gao,Kang Wang,Qiao-gang Wang,Chuan Qin,Xiangxi Wang +13 more
TL;DR: Omicron, with a dramatically increased infectivity and enhanced transmissibility, is rapidly replacing the Delta variant and is poised to become a predominately prevalent strain in more than 110 countries since it was reported in South Africa at the end of 2021.