TY - JOUR
T1 - Seroprevalence of anti-SARS-CoV-2 antibodies and cross-variant neutralization capacity after the Omicron BA.2 wave in Geneva, Switzerland
T2 - a population-based study
AU - Specchio-COVID19 Study Group
AU - Zaballa, María Eugenia
AU - Perez-Saez, Javier
AU - de Mestral, Carlos
AU - Pullen, Nick
AU - Lamour, Julien
AU - Turelli, Priscilla
AU - Raclot, Charlène
AU - Baysson, Hélène
AU - Pennacchio, Francesco
AU - Villers, Jennifer
AU - Duc, Julien
AU - Richard, Viviane
AU - Dumont, Roxane
AU - Semaani, Claire
AU - Loizeau, Andrea Jutta
AU - Graindorge, Clément
AU - Lorthe, Elsa
AU - Balavoine, Jean François
AU - Pittet, Didier
AU - Schibler, Manuel
AU - Vuilleumier, Nicolas
AU - Chappuis, François
AU - Kherad, Omar
AU - Azman, Andrew S.
AU - Posfay-Barbe, Klara M.
AU - Kaiser, Laurent
AU - Trono, Didier
AU - Stringhini, Silvia
AU - Guessous, Idris
AU - Arm-Vernez, Isabelle
AU - Azman, Andrew S.
AU - Bachmann, Delphine
AU - Bal, Antoine
AU - Balavoine, Michael
AU - Barbe, Rémy P.
AU - Beigbeder, Lison
AU - Berthelot, Julie
AU - Bleich, Patrick
AU - Boehm, Livia
AU - Bryand, Gaëlle
AU - Collombet, Prune
AU - Coudurier-Boeuf, Sophie
AU - Courvoisier, Delphine
AU - Cudet, Alain
AU - Davidovic, Vladimir
AU - D'ippolito, Paola
AU - Dubos, Richard
AU - Eckerle, Isabella
AU - El Merjani, Nacira
AU - Flahault, Antoine
N1 - Publisher Copyright:
© 2022 The Authors
PY - 2023/1
Y1 - 2023/1
N2 - Background: More than two years into the COVID-19 pandemic, most of the population has developed anti-SARS-CoV-2 antibodies from infection and/or vaccination. However, public health decision-making is hindered by the lack of up-to-date and precise characterization of the immune landscape in the population. Here, we estimated anti-SARS-CoV-2 antibodies seroprevalence and cross-variant neutralization capacity after Omicron became dominant in Geneva, Switzerland. Methods: We conducted a population-based serosurvey between April 29 and June 9, 2022, recruiting children and adults of all ages from age-stratified random samples of the general population of Geneva, Switzerland. We tested for anti-SARS-CoV-2 antibodies using commercial immunoassays targeting either the spike (S) or nucleocapsid (N) protein, and for antibody neutralization capacity against different SARS-CoV-2 variants using a cell-free Spike trimer-ACE2 binding-based surrogate neutralization assay. We estimated seroprevalence and neutralization capacity using a Bayesian modeling framework accounting for the demographics, vaccination, and infection statuses of the Geneva population. Findings: Among the 2521 individuals included in the analysis, the estimated total antibodies seroprevalence was 93.8% (95% CrI 93.1–94.5), including 72.4% (70.0–74.7) for infection-induced antibodies. Estimates of neutralizing antibodies in a representative subsample (N = 1160) ranged from 79.5% (77.1–81.8) against the Alpha variant to 46.7% (43.0–50.4) against the Omicron BA.4/BA.5 subvariants. Despite having high seroprevalence of infection-induced antibodies (76.7% [69.7–83.0] for ages 0–5 years, 90.5% [86.5–94.1] for ages 6–11 years), children aged <12 years had substantially lower neutralizing activity than older participants, particularly against Omicron subvariants. Overall, vaccination was associated with higher neutralizing activity against pre-Omicron variants. Vaccine booster alongside recent infection was associated with higher neutralizing activity against Omicron subvariants. Interpretation: While most of the Geneva population has developed anti-SARS-CoV-2 antibodies through vaccination and/or infection, less than half has neutralizing activity against the currently circulating Omicron BA.5 subvariant. Hybrid immunity obtained through booster vaccination and infection confers the greatest neutralization capacity, including against Omicron. Funding: General Directorate of Health in Geneva canton, Private Foundation of the Geneva University Hospitals, European Commission (“CoVICIS” grant), and a private foundation advised by CARIGEST SA.
AB - Background: More than two years into the COVID-19 pandemic, most of the population has developed anti-SARS-CoV-2 antibodies from infection and/or vaccination. However, public health decision-making is hindered by the lack of up-to-date and precise characterization of the immune landscape in the population. Here, we estimated anti-SARS-CoV-2 antibodies seroprevalence and cross-variant neutralization capacity after Omicron became dominant in Geneva, Switzerland. Methods: We conducted a population-based serosurvey between April 29 and June 9, 2022, recruiting children and adults of all ages from age-stratified random samples of the general population of Geneva, Switzerland. We tested for anti-SARS-CoV-2 antibodies using commercial immunoassays targeting either the spike (S) or nucleocapsid (N) protein, and for antibody neutralization capacity against different SARS-CoV-2 variants using a cell-free Spike trimer-ACE2 binding-based surrogate neutralization assay. We estimated seroprevalence and neutralization capacity using a Bayesian modeling framework accounting for the demographics, vaccination, and infection statuses of the Geneva population. Findings: Among the 2521 individuals included in the analysis, the estimated total antibodies seroprevalence was 93.8% (95% CrI 93.1–94.5), including 72.4% (70.0–74.7) for infection-induced antibodies. Estimates of neutralizing antibodies in a representative subsample (N = 1160) ranged from 79.5% (77.1–81.8) against the Alpha variant to 46.7% (43.0–50.4) against the Omicron BA.4/BA.5 subvariants. Despite having high seroprevalence of infection-induced antibodies (76.7% [69.7–83.0] for ages 0–5 years, 90.5% [86.5–94.1] for ages 6–11 years), children aged <12 years had substantially lower neutralizing activity than older participants, particularly against Omicron subvariants. Overall, vaccination was associated with higher neutralizing activity against pre-Omicron variants. Vaccine booster alongside recent infection was associated with higher neutralizing activity against Omicron subvariants. Interpretation: While most of the Geneva population has developed anti-SARS-CoV-2 antibodies through vaccination and/or infection, less than half has neutralizing activity against the currently circulating Omicron BA.5 subvariant. Hybrid immunity obtained through booster vaccination and infection confers the greatest neutralization capacity, including against Omicron. Funding: General Directorate of Health in Geneva canton, Private Foundation of the Geneva University Hospitals, European Commission (“CoVICIS” grant), and a private foundation advised by CARIGEST SA.
KW - Anti-SARS-CoV-2 antibodies
KW - Neutralizing antibodies
KW - Omicron
KW - Seroprevalence
KW - Switzerland
KW - Variants of concern
UR - https://www.scopus.com/pages/publications/85143276033
UR - https://www.scopus.com/pages/publications/85143276033#tab=citedBy
U2 - 10.1016/j.lanepe.2022.100547
DO - 10.1016/j.lanepe.2022.100547
M3 - Article
C2 - 36474728
AN - SCOPUS:85143276033
SN - 2666-7762
VL - 24
JO - The Lancet Regional Health - Europe
JF - The Lancet Regional Health - Europe
M1 - 100547
ER -