Magnitude and Kinetics of Anti–Severe Acute Respiratory Syndrome Coronavirus 2 Antibody Responses and Their Relationship to Disease Severity

Author:

Lynch Kara L1ORCID,Whitman Jeffrey D1,Lacanienta Noreen P1,Beckerdite Erica W1,Kastner Shannon A1,Shy Brian R1,Goldgof Gregory M1,Levine Andrew G1,Bapat Sagar P1,Stramer Susan L2,Esensten Jonathan H1,Hightower Allen W3,Bern Caryn4,Wu Alan H B1

Affiliation:

1. Department of Laboratory Medicine, University of California, San Francisco, San Francisco, California, USA

2. Scientific Affairs, American Red Cross, Gaithersberg, Maryland, USA

3. Independent consultant, Bangkok, Thailand

4. Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California, USA

Abstract

Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can be detected indirectly by measuring the host immune response. For some viruses, antibody concentrations correlate with host protection and viral neutralization, but in rare cases, antiviral antibodies can promote disease progression. Elucidation of the kinetics and magnitude of the SARS-CoV-2 antibody response is essential to understand the pathogenesis of coronavirus disease 2019 (COVID-19) and identify potential therapeutic targets. Methods Sera (n = 533) from patients with real-time polymerase chain reaction–confirmed COVID-19 (n = 94 with acute infections and n = 59 convalescent patients) were tested using a high-throughput quantitative immunoglobulin M (IgM) and immunoglobulin G (IgG) assay that detects antibodies to the spike protein receptor binding domain and nucleocapsid protein. Individual and serial samples covered the time of initial diagnosis, during the disease course, and following recovery. We evaluated antibody kinetics and correlation between magnitude of the response and disease severity. Results Patterns of SARS-CoV-2 antibody production varied considerably. Among 52 patients with 3 or more serial specimens, 44 (84.6%) and 42 (80.8%) had observed IgM and IgG seroconversion at a median of 8 and 10 days, respectively. Compared to those with milder disease, peak measurements were significantly higher for patients admitted to the intensive care unit for all time intervals between 6 and 20 days for IgM, and all intervals after 5 days for IgG. Conclusions High-sensitivity assays with a robust dynamic range provide a comprehensive picture of host antibody response to SARS-CoV-2. IgM and IgG responses were significantly higher in patients with severe than mild disease. These differences may affect strategies for seroprevalence studies, therapeutics, and vaccine development.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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