TY - JOUR
T1 - Seroprevalence of anti-SARS-CoV-2 antibodies in COVID-19 patients and healthy volunteers up to 6 months post disease onset
AU - Figueiredo-Campos, Patrícia
AU - Blankenhaus, Birte
AU - Mota, Catarina
AU - Gomes, Andreia
AU - Serrano, Marta
AU - Ariotti, Silvia
AU - Costa, Catarina
AU - Nunes-Cabaço, Helena
AU - Mendes, António M.
AU - Gaspar, Pedro
AU - Pereira-Santos, M. Conceição
AU - Rodrigues, Fabiana
AU - Condeço, Jorge
AU - Escoval, M. Antonia
AU - Santos, Matilde
AU - Ramirez, Mario
AU - Melo-Cristino, José
AU - Simas, J. Pedro
AU - Vasconcelos, Eugenia
AU - Afonso, Ângela
AU - Veldhoen, Marc
N1 - Funding Information:
We would like to acknowledge the generous sharing of the expression constructs by Drs Florian Krammer and Benhur Lee, Icahn School of Medicine at Mount Sinai, New York, USA (Development of SARS‐CoV‐2 reagents was partially supported by the NIAID Centers of Excellence for Influenza Research and Surveillance (CEIRS) contract HHSN272201400008C), and the protein production by Drs Paula Alves, Pedro Cruz, and Rute Castro at Instituto de Biologia Experimental e Tecnológica (iBET) Oeiras, Portugal as part of the Serology4COVID consortium.
Funding Information:
We would like to thank all volunteers who helped with blood collections (AR Pires, A Ramalho‐dos‐Santos, A Biscaia‐Santos, F Ribeiro, S Caetano, P Napoleão, MJ Silva, P Alves, R Pedroso, P Corredeira, A Friães, M De Niz, I Bento, S Pereira, S Mensurado) and donors and patients for providing blood samples and cooperation to make this study possible. Serum samples were requested from Biobanco‐IMM, Lisbon Academic Medical Centre, Lisbon, Portugal. We like to acknowledge the funding from the European Union H2020 ERA project (No 667824 – EXCELLtoINNOV) and the Fundação para a Ciência e a Tecnologia (FCT) to P.F‐C. (SFRH/BD/131605/2017), PTDC/MED‐IMU/28003/2017, and research4COVID19 (no. 231_596873172, Generating SARS‐CoV2 seroconversion assay and no. 729, High‐throughput SARS‐CoV2 neutralizing antibodies assessment), with additional support by Sociedade Francisco Manuel dos Santos.
Funding Information:
We would like to thank all volunteers who helped with blood collections (AR Pires, A Ramalho-dos-Santos, A Biscaia-Santos, F Ribeiro, S Caetano, P Napoleão, MJ Silva, P Alves, R Pedroso, P Corredeira, A Friães, M De Niz, I Bento, S Pereira, S Mensurado) and donors and patients for providing blood samples and cooperation to make this study possible. Serum samples were requested from Biobanco-IMM, Lisbon Academic Medical Centre, Lisbon, Portugal. We like to acknowledge the funding from the European Union H2020 ERA project (No 667824 – EXCELLtoINNOV) and the Fundação para a Ciência e a Tecnologia (FCT) to P.F-C. (SFRH/BD/131605/2017), PTDC/MED-IMU/28003/2017, and research4COVID19 (no. 231_596873172, Generating SARS-CoV2 seroconversion assay and no. 729, High-throughput SARS-CoV2 neutralizing antibodies assessment), with additional support by Sociedade Francisco Manuel dos Santos. We would like to acknowledge the generous sharing of the expression constructs by Drs Florian Krammer and Benhur Lee, Icahn School of Medicine at Mount Sinai, New York, USA (Development of SARS-CoV-2 reagents was partially supported by the NIAID Centers of Excellence for Influenza Research and Surveillance (CEIRS) contract HHSN272201400008C), and the protein production by Drs Paula Alves, Pedro Cruz, and Rute Castro at Instituto de Biologia Experimental e Tecnológica (iBET) Oeiras, Portugal as part of the Serology4COVID consortium.
Publisher Copyright:
© 2020 The Authors. European Journal of Immunology published by Wiley-VCH GmbH
PY - 2020/12
Y1 - 2020/12
N2 - SARS-CoV-2 has emerged as a human pathogen, causing clinical signs, from fever to pneumonia—COVID-19—but may remain mild or asymptomatic. To understand the continuing spread of the virus, to detect those who are and were infected, and to follow the immune response longitudinally, reliable and robust assays for SARS-CoV-2 detection and immunological monitoring are needed. We quantified IgM, IgG, and IgA antibodies recognizing the SARS-CoV-2 receptor-binding domain (RBD) or the Spike (S) protein over a period of 6 months following COVID-19 onset. We report the detailed setup to monitor the humoral immune response from over 300 COVID-19 hospital patients and healthcare workers, 2500 University staff, and 198 post-COVID-19 volunteers. Anti-SARS-CoV-2 antibody responses follow a classic pattern with a rapid increase within the first three weeks after symptoms. Although titres reduce subsequently, the ability to detect anti-SARS-CoV-2 IgG antibodies remained robust with confirmed neutralization activity for up to 6 months in a large proportion of previously virus-positive screened subjects. Our work provides detailed information for the assays used, facilitating further and longitudinal analysis of protective immunity to SARS-CoV-2. Importantly, it highlights a continued level of circulating neutralising antibodies in most people with confirmed SARS-CoV-2.
AB - SARS-CoV-2 has emerged as a human pathogen, causing clinical signs, from fever to pneumonia—COVID-19—but may remain mild or asymptomatic. To understand the continuing spread of the virus, to detect those who are and were infected, and to follow the immune response longitudinally, reliable and robust assays for SARS-CoV-2 detection and immunological monitoring are needed. We quantified IgM, IgG, and IgA antibodies recognizing the SARS-CoV-2 receptor-binding domain (RBD) or the Spike (S) protein over a period of 6 months following COVID-19 onset. We report the detailed setup to monitor the humoral immune response from over 300 COVID-19 hospital patients and healthcare workers, 2500 University staff, and 198 post-COVID-19 volunteers. Anti-SARS-CoV-2 antibody responses follow a classic pattern with a rapid increase within the first three weeks after symptoms. Although titres reduce subsequently, the ability to detect anti-SARS-CoV-2 IgG antibodies remained robust with confirmed neutralization activity for up to 6 months in a large proportion of previously virus-positive screened subjects. Our work provides detailed information for the assays used, facilitating further and longitudinal analysis of protective immunity to SARS-CoV-2. Importantly, it highlights a continued level of circulating neutralising antibodies in most people with confirmed SARS-CoV-2.
KW - COVID-19
KW - Neutralizing antibodies
KW - SARS-CoV-2
KW - Seroprevalence
UR - http://www.scopus.com/inward/record.url?scp=85096933476&partnerID=8YFLogxK
U2 - 10.1002/eji.202048970
DO - 10.1002/eji.202048970
M3 - Article
C2 - 33084029
AN - SCOPUS:85096933476
SN - 0014-2980
VL - 50
SP - 2025
EP - 2040
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 12
ER -