Longitudinal Serological Analysis and Neutralizing Antibody Levels in Coronavirus Disease 2019 Convalescent Patients

Author:

Muecksch Frauke1,Wise Helen2,Batchelor Becky2,Squires Maria2,Semple Elizabeth2,Richardson Claire3,McGuire Jacqueline3,Clearly Sarah3,Furrie Elizabeth4,Greig Neil4,Hay Gordon4,Templeton Kate2,Lorenzi Julio C C5,Hatziioannou Theodora1,Jenks Sara2,Bieniasz Paul D16ORCID

Affiliation:

1. Laboratory of Retrovirology, The Rockefeller University, New York, New York, USA

2. Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, Scotland

3. University Hospital Monklands, NHS Lanarkshire, Airdrie, Scotland

4. Ninewells Hospital and Medical School, NHS Tayside, Dundee, Scotland

5. Laboratory of Molecular Immunology, The Rockefeller University, New York, New York, USA

6. Howard Hughes Medical Institute, The Rockefeller University, New York, New York, USA

Abstract

Abstract Background Understanding the longitudinal trajectory of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies is crucial for diagnosis of prior infection and predicting future immunity. Methods We conducted a longitudinal analysis of coronavirus disease 2019 convalescent patients, with neutralizing antibody assays and SARS-CoV-2 serological assay platforms using SARS-CoV-2 spike (S) or nucleocapsid (N) antigens. Results Sensitivities of serological assays in diagnosing prior SARS-CoV-2 infection changed with time. One widely used commercial platform that had an initial sensitivity of >95% declined to 71% at 81–100 days after diagnosis. The trajectories of median binding antibody titers measured over approximately 3–4 months were not dependent on the use of SARS-CoV-2 N or S proteins as antigen. The median neutralization titer decreased by approximately 45% per month. Each serological assay gave quantitative antibody titers that were correlated with SARS-CoV-2 neutralization titers, but S-based serological assay measurements better predicted neutralization potency. Correlation between S-binding and neutralization titers deteriorated with time, and decreases in neutralization titers were not predicted by changes in S-binding antibody titers. Conclusions Different SARS-CoV-2 serological assays are more or less well suited for surveillance versus prediction of serum neutralization potency. Extended follow-up should facilitate the establishment of appropriate serological correlates of protection against SARS-CoV-2 reinfection.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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