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Long term anti-SARS-CoV-2 antibody kinetics and correlate of protection against Omicron BA.1/BA.2 infection.
Perez-Saez, Javier; Zaballa, María-Eugenia; Lamour, Julien; Yerly, Sabine; Dubos, Richard; Courvoisier, Delphine S; Villers, Jennifer; Balavoine, Jean-François; Pittet, Didier; Kherad, Omar; Vuilleumier, Nicolas; Kaiser, Laurent; Guessous, Idris; Stringhini, Silvia; Azman, Andrew S.
Afiliação
  • Perez-Saez J; Unit of Population Epidemiology, Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland. javier.perez@hcuge.ch.
  • Zaballa ME; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA. javier.perez@hcuge.ch.
  • Lamour J; Unit of Population Epidemiology, Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Yerly S; Unit of Population Epidemiology, Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Dubos R; Division of Laboratory Medicine, Department of Diagnostics, Geneva University Hospitals, Geneva, Switzerland.
  • Courvoisier DS; Unit of Population Epidemiology, Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Villers J; General Directorate of Health, Geneva, Switzerland.
  • Balavoine JF; Division of Quality of Care, Geneva University Hospitals, Geneva, Switzerland.
  • Pittet D; Unit of Population Epidemiology, Division of Primary Care Medicine, Geneva University Hospitals, Geneva, Switzerland.
  • Kherad O; Department of Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Vuilleumier N; Department of Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Kaiser L; Infection Control Program and World Health Organization Collaborating Centre on Patient Safety, Geneva University Hospitals, Geneva, Switzerland.
  • Guessous I; Department of Medicine, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Stringhini S; Division of Internal Medicine, Hôpital de la Tour, Geneva, Switzerland.
  • Azman AS; Division of Laboratory Medicine, Department of Diagnostics, Geneva University Hospitals, Geneva, Switzerland.
Nat Commun ; 14(1): 3032, 2023 05 26.
Article em En | MEDLINE | ID: mdl-37230973
ABSTRACT
Binding antibody levels against SARS-CoV-2 have shown to be correlates of protection against infection with pre-Omicron lineages. This has been challenged by the emergence of immune-evasive variants, notably the Omicron sublineages, in an evolving immune landscape with high levels of cumulative incidence and vaccination coverage. This in turn limits the use of widely available commercial high-throughput methods to quantify binding antibodies as a tool to monitor protection at the population-level. Here we show that anti-Spike RBD antibody levels, as quantified by the immunoassay used in this study, are an indirect correlate of protection against Omicron BA.1/BA.2 for individuals previously infected by SARS-CoV-2. Leveraging repeated serological measurements between April 2020 and December 2021 on 1083 participants of a population-based cohort in Geneva, Switzerland, and using antibody kinetic modeling, we found up to a three-fold reduction in the hazard of having a documented positive SARS-CoV-2 infection during the Omicron BA.1/BA.2 wave for anti-S antibody levels above 800 IU/mL (HR 0.30, 95% CI 0.22-0.41). However, we did not detect a reduction in hazard among uninfected participants. These results provide reassuring insights into the continued interpretation of SARS-CoV-2 binding antibody measurements as an independent marker of protection at both the individual and population levels.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article