Convergent antibody responses to SARS-CoV-2 in convalescent individuals

被引:0
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作者
Davide F. Robbiani
Christian Gaebler
Frauke Muecksch
Julio C. C. Lorenzi
Zijun Wang
Alice Cho
Marianna Agudelo
Christopher O. Barnes
Anna Gazumyan
Shlomo Finkin
Thomas Hägglöf
Thiago Y. Oliveira
Charlotte Viant
Arlene Hurley
Hans-Heinrich Hoffmann
Katrina G. Millard
Rhonda G. Kost
Melissa Cipolla
Kristie Gordon
Filippo Bianchini
Spencer T. Chen
Victor Ramos
Roshni Patel
Juan Dizon
Irina Shimeliovich
Pilar Mendoza
Harald Hartweger
Lilian Nogueira
Maggi Pack
Jill Horowitz
Fabian Schmidt
Yiska Weisblum
Eleftherios Michailidis
Alison W. Ashbrook
Eric Waltari
John E. Pak
Kathryn E. Huey-Tubman
Nicholas Koranda
Pauline R. Hoffman
Anthony P. West
Charles M. Rice
Theodora Hatziioannou
Pamela J. Bjorkman
Paul D. Bieniasz
Marina Caskey
Michel C. Nussenzweig
机构
[1] The Rockefeller University,Laboratory of Molecular Immunology
[2] The Rockefeller University,Laboratory of Retrovirology
[3] California Institute of Technology,Division of Biology and Biological Engineering
[4] The Rockefeller University,Hospital Program Direction
[5] The Rockefeller University,Laboratory of Virology and Infectious Disease
[6] The Rockefeller University,Center for Clinical Translational Science
[7] Chan Zuckerberg Biohub,Howard Hughes Medical Institute
[8] The Rockefeller University,Institute for Research in Biomedicine
[9] Università della Svizzera italiana,undefined
来源
Nature | 2020年 / 584卷
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摘要
During the coronavirus disease-2019 (COVID-19) pandemic, severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2) has led to the infection of millions of people and has claimed hundreds of thousands of lives. The entry of the virus into cells depends on the receptor-binding domain (RBD) of the spike (S) protein of SARS-CoV-2. Although there is currently no vaccine, it is likely that antibodies will be essential for protection. However, little is known about the human antibody response to SARS-CoV-21–5. Here we report on 149 COVID-19-convalescent individuals. Plasma samples collected an average of 39 days after the onset of symptoms had variable half-maximal pseudovirus neutralizing titres; titres were less than 50 in 33% of samples, below 1,000 in 79% of samples and only 1% of samples had titres above 5,000. Antibody sequencing revealed the expansion of clones of RBD-specific memory B cells that expressed closely related antibodies in different individuals. Despite low plasma titres, antibodies to three distinct epitopes on the RBD neutralized the virus with half-maximal inhibitory concentrations (IC50 values) as low as 2 ng ml−1. In conclusion, most convalescent plasma samples obtained from individuals who recover from COVID-19 do not contain high levels of neutralizing activity. Nevertheless, rare but recurring RBD-specific antibodies with potent antiviral activity were found in all individuals tested, suggesting that a vaccine designed to elicit such antibodies could be broadly effective.
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页码:437 / 442
页数:5
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