Cross-reactive Antibody Response between SARS-CoV-2 and SARS-CoV Infections
Author(s) -
Huibin Lv,
Nicholas C. Wu,
Owen Tak-Yin Tsang,
Meng Yuan,
Ranawaka A. P. M. Perera,
Wai-Shing Leung,
Ray T. Y. So,
Jacky Man Chun Chan,
Garrick K. Yip,
Thomas Shiu Hong Chik,
Yiquan Wang,
Chris Yau Chung Choi,
YiHan Lin,
Wilson W. Ng,
Jincun Zhao,
Leo L. M. Poon,
Malik Peiris,
Ian A. Wilson,
Chris Ka Pun Mok
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2020.107725
Subject(s) - immunogen , antigenicity , virology , antibody , neutralization , epitope , neutralizing antibody , original antigenic sin , cross reactivity , antibody response , coronavirus , covid-19 , biology , antigen , pandemic , outbreak , immunology , disease , medicine , infectious disease (medical specialty) , monoclonal antibody , antigenic drift , cross reactions , hemagglutinin (influenza) , pathology
The World Health Organization has declared the ongoing outbreak of COVID-19, which is caused by a novel coronavirus SARS-CoV-2, as pandemic. There is currently a lack of knowledge about the antibody response elicited from SARS-CoV-2 infection. One major immunological question concerns antigenic differences between SARS-CoV-2 and SARS-CoV. We address this question by analyzing plasma from patients infected by SARS-CoV-2 or SARS-CoV, and from infected or immunized mice. Our results show that, while cross-reactivity in antibody binding to the spike protein is common, cross-neutralization of the live viruses may be rare, indicating the presence of non-neutralizing antibody response to conserved epitopes in the spike. Whether such low or non-neutralizing antibody response leads to antibody-dependent disease enhancement needs to be addressed in the future. Overall, this study not only addresses a fundamental question regarding antigenicity differences between SARS-CoV-2 and SARS-CoV, but also has implications for immunogen design and vaccine development.
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