Nucleocapsid Antigenemia Is a Marker of Acute SARS-CoV-2 Infection

Author:

Verkerke Hans P12ORCID,Damhorst Gregory L34,Graciaa Daniel S3,McLendon Kaleb1,O’Sick William1,Robichaux Chad5,Cheedarla Narayanaiah1,Potlapalli Sindhu1,Wu Shang-Chuen2,Harrington Kristin R V6,Webster Andrew3,Kraft Colleen3,Rostad Christina A7,Waggoner Jesse J3457,Gandhi Neel R36,Guarner Jeannette1ORCID,Auld Sara C68,Neish Andrew1,Roback John D1,Lam Wilbur A47910,Shah N Sarita36,Stowell Sean R2ORCID

Affiliation:

1. Department of Pathology and Laboratory Medicine, Emory University School of Medicine , Atlanta, Georgia , USA

2. Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School , Boston, Massachusetts , USA

3. Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine , Atlanta, Georgia , USA

4. The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies , Atlanta, Georgia , USA

5. Emory Healthcare , Atlanta, Georgia , USA

6. Department of Epidemiology, Emory University Rollins School of Public Health , Atlanta, Georgia , USA

7. Department of Pediatrics and Center for Childhood Infections and Vaccines, Emory University School of Medicine and Children’s Healthcare of Atlanta , Atlanta, Georgia , USA

8. Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Emory University School of Medicine , Atlanta, Georgia , USA

9. Aflac Cancer and Blood Disorders Center at Children’s Healthcare of Atlanta , Atlanta, Georgia , USA

10. Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology , Atlanta, Georgia , USA

Abstract

Abstract Detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is essential for diagnosis, treatment, and infection control. Polymerase chain reaction (PCR) fails to distinguish acute from resolved infections, as RNA is frequently detected after infectiousness. We hypothesized that nucleocapsid in blood marks acute infection with the potential to enhance isolation and treatment strategies. In a retrospective serosurvey of inpatient and outpatient encounters, we categorized samples along an infection timeline using timing of SARS-CoV-2 testing and symptomatology. Among 1860 specimens from 1607 patients, the highest levels and frequency of antigenemia were observed in samples from acute SARS-CoV-2 infection. Antigenemia was higher in seronegative individuals and in those with severe disease. In our analysis, antigenemia exhibited 85.8% sensitivity and 98.6% specificity as a biomarker for acute coronavirus disease 2019 (COVID-19). Thus, antigenemia sensitively and specifically marks acute SARS-CoV-2 infection. Further study is warranted to determine whether antigenemia may aid individualized assessment of active COVID-19.

Funder

Woodruff Health Sciences Center

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference30 articles.

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