Development of a Potent and Protective Germline-Like Antibody Lineage Against Zika Virus in a Convalescent Human

被引:13
作者
Gao, Fei [1 ]
Lin, Xiaohe [2 ]
He, Linling [2 ]
Wang, Ruoke [1 ]
Wang, Han [1 ]
Shi, Xuanling [1 ]
Zhang, Fuchun [3 ]
Yin, Chibiao [3 ]
Zhang, Linqi [1 ]
Zhu, Jiang [2 ]
Yu, Lei [3 ]
机构
[1] Tsinghua Univ, Sch Med, Beijing Adv Innovat Ctr Struct Biol, Dept Basic Med Sci,Comprehens AIDS Res Ctr, Beijing, Peoples R China
[2] Scripps Res Inst, Dept Immunol & Microbiol, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
[3] Guangzhou Med Univ, Guangzhou Peoples Hosp 8, Guangzhou, Guangdong, Peoples R China
关键词
Zika virus infection; Guillain-Barre syndrome; microcephaly; neutralizing antibody; antibody repertoire; next-generation sequencing; NEUTRALIZING HUMAN-ANTIBODIES; STRUCTURAL BASIS; HIV-1-NEUTRALIZING ANTIBODIES; INFECTION; PROTEIN; MICE;
D O I
10.3389/fimmu.2019.02424
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Zika virus (ZIKV) specific neutralizing antibodies hold great promise for antibody-based interventions and vaccine design against ZIKV infection. However, their development in infected patients remains unclear. Here, we applied next-generation sequencing (NGS) to probe the dynamic development of a potent and protective ZIKV E DIII-specific antibody ZK2B10 isolated from a ZIKV convalescent individual. The unbiased repertoire analysis showed dramatic changes in the usage of antibody variable region germline genes. However, lineage tracing of ZK2B10 revealed limited somatic hypermutation and transient expansion during the 12 months following the onset of symptoms. The NGS-derived, germline-like ZK2B10 somatic variants neutralized ZIKV potently and protected mice from lethal challenge of ZIKV without detectable cross-reactivity with Dengue virus (DENV). Site-directed mutagenesis identified two residues within the lambda chain, N31 and S91, that are essential to the functional maturation of ZK2B10. The repertoire and lineage features unveiled here will help elucidate the developmental process and protective potential of E DIII-directed antibodies against ZIKV infection.
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页数:13
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