TY - JOUR
T1 - Seroprevalence of anti-SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP)
T2 - a population-based study
AU - Stringhini, Silvia
AU - Wisniak, Ania
AU - Piumatti, Giovanni
AU - Azman, Andrew S.
AU - Lauer, Stephen A.
AU - Baysson, Hélène
AU - De Ridder, David
AU - Petrovic, Dusan
AU - Schrempft, Stephanie
AU - Marcus, Kailing
AU - Yerly, Sabine
AU - Arm Vernez, Isabelle
AU - Keiser, Olivia
AU - Hurst, Samia
AU - Posfay-Barbe, Klara M.
AU - Trono, Didier
AU - Pittet, Didier
AU - Gétaz, Laurent
AU - Chappuis, François
AU - Eckerle, Isabella
AU - Vuilleumier, Nicolas
AU - Meyer, Benjamin
AU - Flahault, Antoine
AU - Kaiser, Laurent
AU - Guessous, Idris
N1 - Funding Information:
This study would not have been possible without the instrumental and passionate contribution of the staff of the Unit of Population Epidemiology of the HUG Primary Care Division, Geneva University Hospitals, Geneva, Switzerland (Natacha Noel, Caroline Pugin, Jane Portier, Barinjaka Rakotomiaramanana, Leila Botudi, Natalie Francioli, Paola d'Ippolito, Chantal Martinez, Francesco Pennacchio, Benjamin Emery, Zoé Waldman, Magdalena Schellongova, Aude Richard, Prune Collombet, and Attilio Picazio), of the team of the Division of Laboratory Medicine, Geneva University Hospitals (Géraldine Poulain and Pierre Lescuyer), of the Geneva University Hospitals staff affected to our unit during the COVID-19 emergency (Lilas Salzmann-Bellard, Mélanie Seixas Miranda, Yasmina Malim, Acem Gonul, and Odile Desvachez), Loan Mattera and all the personnel of Campus Biotech, and finally without the invaluable work of the medical students who have invested their time and energy in this project (Jonathan Barbolini, Eugénie de Weck, Natacha Michel, Emmanuelle Mohbat, Irine Sakvarelidze, Céline Eelbode, Sultan Bahta, Céline Dubas, Lina Hassar, Melis Kir, Hugo-Ken Oulevey, Kourosh Massiha, Manon Will, Natacha Vincent, Fanny Lombard, Alioucha Davidovic, Benoit Favre, Amélie Mach, Eva Marchetti, Sophie Cattani, Joséphine Duc, Julie Guérin, Soraya Maret, Francesca Hovagemyan, Antoine Daeniker, and Rebecca Buetzberger). We also thank Nicola Low for her insight and help in designing the study, Markus Hoffmann and Stefan Pöhlmann (Georg-August-Universität Göttingen, Göttingen, Germany) for providing the SARS-CoV-2 spike expression vector used in the recombinant immunofluorescence, the Geneva University Hospitals archives, Human Neuroscience Platform, Fondation Campus Biotech Geneva for allowing us to use their premises for recruitment, and all the participants of the Bus Santé study and their household members. This study was funded by the Swiss Federal Office of Public Health, the Corona Immunitas research program of the Swiss School of Public Health, the Fondation de Bienfaisance du Groupe Pictet, the Fondation Ancrage, the Fondation Privée des HUG, and the Center for Emerging Viral Diseases. ASA and SAL are funded by the US National Institutes of Health (R01 AI135115) and The Bill & Melinda Gates Foundation (OPP1191944).
Funding Information:
This study would not have been possible without the instrumental and passionate contribution of the staff of the Unit of Population Epidemiology of the HUG Primary Care Division, Geneva University Hospitals, Geneva, Switzerland (Natacha Noel, Caroline Pugin, Jane Portier, Barinjaka Rakotomiaramanana, Leila Botudi, Natalie Francioli, Paola d'Ippolito, Chantal Martinez, Francesco Pennacchio, Benjamin Emery, Zoé Waldman, Magdalena Schellongova, Aude Richard, Prune Collombet, and Attilio Picazio), of the team of the Division of Laboratory Medicine, Geneva University Hospitals (Géraldine Poulain and Pierre Lescuyer), of the Geneva University Hospitals staff affected to our unit during the COVID-19 emergency (Lilas Salzmann-Bellard, Mélanie Seixas Miranda, Yasmina Malim, Acem Gonul, and Odile Desvachez), Loan Mattera and all the personnel of Campus Biotech, and finally without the invaluable work of the medical students who have invested their time and energy in this project (Jonathan Barbolini, Eugénie de Weck, Natacha Michel, Emmanuelle Mohbat, Irine Sakvarelidze, Céline Eelbode, Sultan Bahta, Céline Dubas, Lina Hassar, Melis Kir, Hugo-Ken Oulevey, Kourosh Massiha, Manon Will, Natacha Vincent, Fanny Lombard, Alioucha Davidovic, Benoit Favre, Amélie Mach, Eva Marchetti, Sophie Cattani, Joséphine Duc, Julie Guérin, Soraya Maret, Francesca Hovagemyan, Antoine Daeniker, and Rebecca Buetzberger). We also thank Nicola Low for her insight and help in designing the study, Markus Hoffmann and Stefan Pöhlmann (Georg-August-Universität Göttingen, Göttingen, Germany) for providing the SARS-CoV-2 spike expression vector used in the recombinant immunofluorescence, the Geneva University Hospitals archives, Human Neuroscience Platform, Fondation Campus Biotech Geneva for allowing us to use their premises for recruitment, and all the participants of the Bus Santé study and their household members. This study was funded by the Swiss Federal Office of Public Health, the Corona Immunitas research program of the Swiss School of Public Health, the Fondation de Bienfaisance du Groupe Pictet, the Fondation Ancrage, the Fondation Privée des HUG, and the Center for Emerging Viral Diseases. ASA and SAL are funded by the US National Institutes of Health (R01 AI135115) and The Bill & Melinda Gates Foundation (OPP1191944).
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Background: Assessing the burden of COVID-19 on the basis of medically attended case numbers is suboptimal given its reliance on testing strategy, changing case definitions, and disease presentation. Population-based serosurveys measuring anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) antibodies provide one method for estimating infection rates and monitoring the progression of the epidemic. Here, we estimate weekly seroprevalence of anti-SARS-CoV-2 antibodies in the population of Geneva, Switzerland, during the epidemic. Methods: The SEROCoV-POP study is a population-based study of former participants of the Bus Santé study and their household members. We planned a series of 12 consecutive weekly serosurveys among randomly selected participants from a previous population-representative survey, and their household members aged 5 years and older. We tested each participant for anti-SARS-CoV-2-IgG antibodies using a commercially available ELISA. We estimated seroprevalence using a Bayesian logistic regression model taking into account test performance and adjusting for the age and sex of Geneva's population. Here we present results from the first 5 weeks of the study. Findings: Between April 6 and May 9, 2020, we enrolled 2766 participants from 1339 households, with a demographic distribution similar to that of the canton of Geneva. In the first week, we estimated a seroprevalence of 4·8% (95% CI 2·4–8·0, n=341). The estimate increased to 8·5% (5·9–11·4, n=469) in the second week, to 10·9% (7·9–14·4, n=577) in the third week, 6·6% (4·3–9·4, n=604) in the fourth week, and 10·8% (8·2–13·9, n=775) in the fifth week. Individuals aged 5–9 years (relative risk [RR] 0·32 [95% CI 0·11–0·63]) and those older than 65 years (RR 0·50 [0·28–0·78]) had a significantly lower risk of being seropositive than those aged 20–49 years. After accounting for the time to seroconversion, we estimated that for every reported confirmed case, there were 11·6 infections in the community. Interpretation: These results suggest that most of the population of Geneva remained uninfected during this wave of the pandemic, despite the high prevalence of COVID-19 in the region (5000 reported clinical cases over <2·5 months in the population of half a million people). Assuming that the presence of IgG antibodies is associated with immunity, these results highlight that the epidemic is far from coming to an end by means of fewer susceptible people in the population. Further, a significantly lower seroprevalence was observed for children aged 5–9 years and adults older than 65 years, compared with those aged 10–64 years. These results will inform countries considering the easing of restrictions aimed at curbing transmission. Funding: Swiss Federal Office of Public Health, Swiss School of Public Health (Corona Immunitas research program), Fondation de Bienfaisance du Groupe Pictet, Fondation Ancrage, Fondation Privée des Hôpitaux Universitaires de Genève, and Center for Emerging Viral Diseases.
AB - Background: Assessing the burden of COVID-19 on the basis of medically attended case numbers is suboptimal given its reliance on testing strategy, changing case definitions, and disease presentation. Population-based serosurveys measuring anti-severe acute respiratory syndrome coronavirus 2 (anti-SARS-CoV-2) antibodies provide one method for estimating infection rates and monitoring the progression of the epidemic. Here, we estimate weekly seroprevalence of anti-SARS-CoV-2 antibodies in the population of Geneva, Switzerland, during the epidemic. Methods: The SEROCoV-POP study is a population-based study of former participants of the Bus Santé study and their household members. We planned a series of 12 consecutive weekly serosurveys among randomly selected participants from a previous population-representative survey, and their household members aged 5 years and older. We tested each participant for anti-SARS-CoV-2-IgG antibodies using a commercially available ELISA. We estimated seroprevalence using a Bayesian logistic regression model taking into account test performance and adjusting for the age and sex of Geneva's population. Here we present results from the first 5 weeks of the study. Findings: Between April 6 and May 9, 2020, we enrolled 2766 participants from 1339 households, with a demographic distribution similar to that of the canton of Geneva. In the first week, we estimated a seroprevalence of 4·8% (95% CI 2·4–8·0, n=341). The estimate increased to 8·5% (5·9–11·4, n=469) in the second week, to 10·9% (7·9–14·4, n=577) in the third week, 6·6% (4·3–9·4, n=604) in the fourth week, and 10·8% (8·2–13·9, n=775) in the fifth week. Individuals aged 5–9 years (relative risk [RR] 0·32 [95% CI 0·11–0·63]) and those older than 65 years (RR 0·50 [0·28–0·78]) had a significantly lower risk of being seropositive than those aged 20–49 years. After accounting for the time to seroconversion, we estimated that for every reported confirmed case, there were 11·6 infections in the community. Interpretation: These results suggest that most of the population of Geneva remained uninfected during this wave of the pandemic, despite the high prevalence of COVID-19 in the region (5000 reported clinical cases over <2·5 months in the population of half a million people). Assuming that the presence of IgG antibodies is associated with immunity, these results highlight that the epidemic is far from coming to an end by means of fewer susceptible people in the population. Further, a significantly lower seroprevalence was observed for children aged 5–9 years and adults older than 65 years, compared with those aged 10–64 years. These results will inform countries considering the easing of restrictions aimed at curbing transmission. Funding: Swiss Federal Office of Public Health, Swiss School of Public Health (Corona Immunitas research program), Fondation de Bienfaisance du Groupe Pictet, Fondation Ancrage, Fondation Privée des Hôpitaux Universitaires de Genève, and Center for Emerging Viral Diseases.
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U2 - 10.1016/S0140-6736(20)31304-0
DO - 10.1016/S0140-6736(20)31304-0
M3 - Article
C2 - 32534626
AN - SCOPUS:85086936792
SN - 0140-6736
VL - 396
SP - 313
EP - 319
JO - The Lancet
JF - The Lancet
IS - 10247
ER -