Cited by 114SARS-CoV-2 and COVID-19 ResearchMonoclonal and Polyclonal Antibodies Researchvaccines and immunoinformatics approaches

A human SARS-CoV neutralizing antibody against epitope on S2 protein

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Duan, Jinzhu, Yan, Xiyun, Guo, Xueming, Cao, Wuchun, Han, Wei, Qi, Cai, Feng, Jing, Yang, Dongling +2 more·2005·Biochemical and Biophysical Research Communications

Abstract

An immune antibody phage-display library was constructed from B cells of SARS convalescent patients. More than 80 clones were selected from the library by using the whole inactivated SARS-CoV virions as target. One human scFv, B1, was characterized extensively. The B1 recognized SARS pseudovirus in vivo and competed with SARS sera for binding to SARS-CoV with high affinity (equilibrium dissociation constant, K(d) = 105 nM). The B1 also has potent neutralizing activities against infection by pseudovirus expressing SARS-CoV S protein in vitro. Finally, we found that the B1 recognized an epitope on S2 protein, especially within amino acids 1023-1189 of S2 protein. This study not only first made a human neutralizing antibody, which recognized an epitope on S2 protein like natural antibody in sera, but also may help us to better understand the immunological characteristics of SARS protein and SARS vaccine design.

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Crossref · 10.1016/j.bbrc.2005.05.089

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  • Targeting the RBD has been a major focus in COVID-19 vaccine development.

    “Eliciting an immune response that targets the RBD has been a major focus of vaccine development on the assumption that antibodies that bind this critical domain can prevent viral entry into host cells, thereby allowing for sterilizing immunity (that is, the complete prevention of infection)152–154, which would support herd immunity if vaccine coverage is sufficiently high155.”

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Research works printed but not linked: 4

  1. [20]O’Philippa M. BrienRobert A. Methods in molecular biology: antibody phage display (methods and protocols) 178 2002 Humana Press Totowa, New Jersey pp. 59–73 and 133–147
  2. [21]Borrebaeck C.A.K. Antibody engineering 1995 Oxford university press New York pp. 53–87
  3. [27]Dong Zh. Wang Y. Antibody engineering second ed. 2002 Peking University Medical Press Beijing pp. 308–315
  4. [28]Sblattero D. Bradbury A. A definitive set of oligonucleotide primers for amplifying human V regions International School for Advanced Studies Immunotechnology 3 1998 271 278 9530560

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Authors
Duan, J., Yan, X., Guo, X., Cao, W., Han, W., Qi, C., Feng, J., Yang, D., Gao, G., & Jin, G.
Affiliations
  • Chinese Academy of Sciences (CN)
  • Institute of Biophysics (CN)
  • Institute of Microbiology (CN)
Corresponding author
Yan, Xiyun
Venue
Biochemical and Biophysical Research Communications
Publisher
Elsevier BV
Published
2005-07
Volume
333
Issue
1
Pages
186-193
ISSN
0006-291X (ISSN-L)
OpenAlex
W2109538392
Cited by
114
References
32
Citations by year
2026: 1 · 2025: 1 · 2023: 5 · 2022: 14 · 2021: 24 · 2020: 29 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 1 · 2014: 2 · 2013: 2 · 2012: 1
FWCI
4.71
Type
journal article
Language
en
Open access
Locations
  • Biochemical and Biophysical Research Communications (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
Keywords
SARS-CoV, neutralizing antibodies, SARS-CoV spike protein, scFv, phage display, B cells, epitope mapping, pseudovirus, natural antibodies
MeSH terms
Antibodies, B-Lymphocytes, Humans, Immunoassay, Neutralization Tests, Viral Envelope Proteins, Epitope Mapping, Epitopes, B-Lymphocyte, Peptide Library, Severe acute respiratory syndrome-related coronavirus

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