Development of a neutralization monoclonal antibody with a broad neutralizing effect against SARS-CoV-2 variants

被引:0
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作者
Ko, Hae Li [1 ,2 ]
Lee, Deuk-ki [1 ,2 ]
Kim, Younghyeon [1 ,2 ]
Jang, Hui Jeong [3 ]
Lee, Youn Woo [3 ]
Lee, Ho-Young [3 ]
Seok, Sang-Hyuk [4 ]
Park, Jun Won [4 ]
Limb, Jin-Kyung [5 ]
On, Da In [5 ,6 ,7 ]
Yun, Jun-Won [8 ]
Lyoo, Kwang-Soo [11 ]
Song, Daesub [12 ,13 ]
Yeom, Minjoo [12 ,13 ]
Lee, Hanbyeul [12 ,13 ]
Seong, Je Kyung [5 ,6 ,7 ,9 ,10 ]
Lee, Sungjin [1 ]
机构
[1] Scripps Korea Antibody Inst, Div Res Program, Chunchon 24341, South Korea
[2] Kangwon Natl Univ, Coll Med Sci, Dept Microbiol, Chuncheon Si 24341, Gangwon Do, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Nucl Med, Seongnam Si 13620, Gyeonggi Do, South Korea
[4] Kangwon Natl Univ, Coll Biomed Sci, Div Biomed Convergence, Chuncheon Si 24341, Gyeonggi Do, South Korea
[5] Seoul Natl Univ, Korea Mouse Phenotyping Ctr KMPC, Seoul 08826, South Korea
[6] Seoul Natl Univ, Res Inst Vet Sci, Coll Vet Med, Lab Dev Biol & Genom, Seoul 08826, South Korea
[7] Seoul Natl Univ, Coll Vet Med, Program Vet Sci BK21, Seoul 08826, South Korea
[8] Seoul Natl Univ, Coll Vet Med, Lab Vet Toxicol, Seoul 08826, South Korea
[9] Seoul Natl Univ, Interdisciplinary Program Bioinformat, Program Canc Biol, Seoul 08826, South Korea
[10] Seoul Natl Univ, BIO MAX N Bio Inst, Seoul 08826, South Korea
[11] Jeonbuk Natl Univ, Coll Vet Med, Iksan 54596, South Korea
[12] Seoul Natl Univ, Coll Vet Med, Dept Vet Med Virol Lab, Seoul 08826, South Korea
[13] Seoul Natl Univ, Res Inst Vet Sci, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
Severe acute respiratory syndrome coronavirus 2; COVID-19; Antibody; Variant of concern; Human angiotensin-converting enzyme 2; Quaternary epitopes of RBD; Single-chain fragment variable; INFECTION;
D O I
10.1186/s12985-023-02230-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundThe emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants has challenged the effectiveness of current therapeutic regimens. Here, we aimed to develop a potent SARS-CoV-2 antibody with broad neutralizing effect by screening a scFv library with the spike protein receptor-binding domain (RBD) via phage display.MethodsSKAI-DS84 was identified through phage display, and we performed pseudovirus neutralization assays, authentic virus neutralization assays, and in vivo neutralization efficacy evaluations. Furthermore, surface plasmon resonance (SPR) analysis was conducted to assess the physical characteristics of the antibody, including binding kinetics and measure its affinity for variant RBDs.ResultsThe selected clones were converted to human IgG, and among them, SKAI-DS84 was selected for further analyses based on its binding affinity with the variant RBDs. Using pseudoviruses, we confirmed that SKAI-DS84 was strongly neutralizing against wild-type, B.1.617.2, B.1.1.529, and subvariants of SARS-CoV-2. We also tested the neutralizing effect of SKAI-DS84 on authentic viruses, in vivo and observed a reduction in viral replication and improved lung pathology. We performed binding and epitope mapping experiments to understand the mechanisms underlying neutralization and identified quaternary epitopes formed by the interaction between RBDs as the target of SKAI-DS84.ConclusionsWe identified, produced, and tested the neutralizing effect of SKAI-DS84 antibody. Our results highlight that SKAI-DS84 could be a potential neutralizing antibody against SARS-CoV-2 and its variants.
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页数:17
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