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Humoral Immunity to SARS-CoV-2 and Inferred Protection from Infection in a French Longitudinal Community Cohort
Tom Woudenberg; Laurie Pinaud; Laura Garcia; Laura Tondeur; Stephane Pelleau; Alix de Thoisy; Francoise Donnadieu; Marija Backovic; Mikael Attia; Nathanael Hoze; Cecile Duru; Aymar Davy Koffi; Sandrine Castelain; Marie-Noelle Ungeheuer; Sandrine Fernandes Pellerin; Delphine Planas; Timothee Bruel; SIMON CAUCHEMEZ; Olivier Schwarz; Arnaud Fontanet; Michael White.
Afiliación
  • Tom Woudenberg; Institut Pasteur
  • Laurie Pinaud; Institut Pasteur
  • Laura Garcia; Institut Pasteur
  • Laura Tondeur; Institut Pasteur
  • Stephane Pelleau; Institut Pasteur
  • Alix de Thoisy; Institut Pasteur
  • Francoise Donnadieu; Institut Pasteur
  • Marija Backovic; Institut Pasteur
  • Mikael Attia; Institut Pasteur
  • Nathanael Hoze; Institut Pasteur
  • Cecile Duru; Hopital de Crepy-en-Valois
  • Aymar Davy Koffi; Hopital de Crepy-en-Valois
  • Sandrine Castelain; CHU Amiens
  • Marie-Noelle Ungeheuer; Institut Pasteur
  • Sandrine Fernandes Pellerin; Institut Pasteur
  • Delphine Planas; Institut Pasteur
  • Timothee Bruel; Institut Pasteur
  • SIMON CAUCHEMEZ; Institut Pasteur
  • Olivier Schwarz; Institut Pasteur
  • Arnaud Fontanet; Institut Pasteur
  • Michael White; Institut Pasteur
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22275460
ABSTRACT
Population-level immunity to SARS-CoV-2 is growing through vaccination as well as ongoing circulation. Given waning immunity and emergence of new variants, it is important to dynamically determine the risk of re-infection in the population. For estimating immune protection, neutralization titers are most informative, but these assays are difficult to conduct at a population level. Measurement of antibody levels can be implemented at high throughput, but has not been robustly validated as a correlate of protection. Here, we have developed a method that predicts neutralization and protection based on variant-specific antibody measurements to SARS-CoV-2 antigens. This approach allowed us to estimate population-immunity in a longitudinal cohort from France followed for up to 2 years. Participants with a single vaccination or immunity caused by infection only are especially vulnerable to COVID-19 or hospitalization due to SARS-CoV-2. While the median reduced risk to COVID-19 in participants with 3 vaccinations was 96%, the median reduced risk among participants with infection-acquired immunity only was 42%. The results presented here are consistent with data from vaccine-effectiveness studies indicating robustness of our approach. Our multiplex serological assay can be readily optimized and employed to study any new variant and provides a framework for development of an assay that would include protection estimates.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Observational_studies / Prognostic_studies Idioma: En Año: 2022 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Observational_studies / Prognostic_studies Idioma: En Año: 2022 Tipo del documento: Preprint