Neutralizing Antibody Levels as a Correlate of Protection Against SARS‐CoV‐2 Infection: A Modeling Analysis

Author:

Lingas Guillaume1ORCID,Planas Delphine23,Péré Hélène45,Porrot Françoise2,Guivel‐Benhassine Florence2,Staropoli Isabelle2,Duffy Darragh6,Chapuis Nicolas7,Gobeaux Camille8,Veyer David45,Delaugerre Constance910,Le Goff Jérôme911,Getten Prunelle12,Hadjadj Jérôme13,Bellino Adèle14,Parfait Béatrice15,Treluyer Jean‐Marc16,Schwartz Olivier23ORCID,Guedj Jérémie1ORCID,Kernéis Solen117,Terrier Benjamin1318

Affiliation:

1. Université Paris Cité, IAME, INSERM Paris France

2. Virus and Immunity Unit Institut Pasteur, Université Paris Cité, CNRS UMR3569 Paris France

3. Vaccine Research Institute Créteil France

4. Virology Unit, Microbiology Department APHP, Hôpital Européen Georges‐Pompidou Paris France

5. Université Paris Cité, INSERM UMRS1138 Functional Genomics of Solid Tumors Laboratory Paris France

6. Translational Immunology Unit Institut Pasteur, Université Paris Cité Paris France

7. Assistance Publique‐Hôpitaux de Paris Centre‐Université Paris Cité, Service d'hématologie biologique, Hôpital Cochin Paris France

8. Department of Automated Biology CHU de Cochin, AP‐HP Paris France

9. Virology Department AP‐HP, Hôpital Saint‐Louis Paris France

10. Université Paris Cité, Inserm U944, Biology of Emerging Viruses Paris France

11. Université Paris Cité, Inserm U976, INSIGHT Team Paris France

12. INSERM UMRS 970 Université Paris Descartes Paris France

13. Department of Internal Medicine National Reference Center for Rare Systemic Autoimmune Diseases, AP‐HP, APHP.CUP, Hôpital Cochin Paris France

14. URC‐CIC Paris Centre Necker/Cochin, AP‐HP, Hôpital Cochin Paris France

15. Fédération des Centres de Ressources Biologiques ‐ Plateformes de Ressources Biologiques AP‐HP.Centre‐Université Paris Cité, Centre de Ressources Biologiques Cochin, Hôpital Cochin Paris France

16. Unité de Recherche clinique, Hôpital Cochin, AP‐HP.Centre ‐ Université de Paris Paris France

17. Equipe de Prévention du Risque Infectieux (EPRI), AP‐HP, Hôpital Bichat Paris France

18. Université Paris Cité, INSERM U970, Paris Cardiovascular Research Center Paris France

Abstract

Although anti‐severe acute respiratory syndrome‐coronavirus 2 antibody kinetics have been described in large populations of vaccinated individuals, we still poorly understand how they evolve during a natural infection and how this impacts viral clearance. For that purpose, we analyzed the kinetics of both viral load and neutralizing antibody levels in a prospective cohort of individuals during acute infection with alpha variant. Using a mathematical model, we show that the progressive increase in neutralizing antibodies leads to a shortening of the half‐life of both infected cells and infectious viral particles. We estimated that the neutralizing activity reached 90% of its maximal level within 11 days after symptom onset and could reduce the half‐life of both infected cells and circulating virus by a 6‐fold factor, thus playing a key role to achieve rapid viral clearance. Using this model, we conducted a simulation study to predict in a more general context the protection conferred by pre‐existing neutralization titers, due to either vaccination or prior infection. We predicted that a neutralizing activity, as measured by 50% effective dose > 103, could reduce by 46% the risk of having viral load detectable by standard polymerase chain reaction assays and by 98% the risk of having viral load above the threshold of infectiousness. Our model shows that neutralizing activity could be used to define correlates of protection against infection and transmission.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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