Simultaneous Quantitative SARS-CoV-2 Antigen and Host Antibody Detection and Pre-Screening Strategy at the Point of Care

Author:

Srinivasan Rajsri Kritika12ORCID,McRae Michael P.1ORCID,Christodoulides Nicolaos J.1ORCID,Dapkins Isaac3ORCID,Simmons Glennon W.1ORCID,Matz Hanover4ORCID,Dooley Helen4ORCID,Fenyö David5ORCID,McDevitt John T.1ORCID

Affiliation:

1. Division of Biomaterials, Department of Molecular Pathobiology, New York University School of Dentistry, New York, NY 10010, USA

2. Department of Pathology, Vilcek Institute of Graduate Biomedical Sciences, New York University School of Medicine, New York, NY 10010, USA

3. Departments of Population Health and Medicine, New York University School of Medicine, New York, NY 10010, USA

4. Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA

5. Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10010, USA

Abstract

As COVID-19 pandemic public health measures are easing globally, the emergence of new SARS-CoV-2 strains continue to present high risk for vulnerable populations. The antibody-mediated protection acquired from vaccination and/or infection is seen to wane over time and the immunocompromised populations can no longer expect benefit from monoclonal antibody prophylaxis. Hence, there is a need to monitor new variants and its effect on vaccine performance. In this context, surveillance of new SARS-CoV-2 infections and serology testing are gaining consensus for use as screening methods, especially for at-risk groups. Here, we described an improved COVID-19 screening strategy, comprising predictive algorithms and concurrent, rapid, accurate, and quantitative SARS-CoV-2 antigen and host antibody testing strategy, at point of care (POC). We conducted a retrospective analysis of 2553 pre- and asymptomatic patients who were tested for SARS-CoV-2 by RT-PCR. The pre-screening model had an AUC (CI) of 0.76 (0.73–0.78). Despite being the default method for screening, body temperature had lower AUC (0.52 [0.49–0.55]) compared to case incidence rate (0.65 [0.62–0.68]). POC assays for SARS-CoV-2 nucleocapsid protein (NP) and spike (S) receptor binding domain (RBD) IgG antibody showed promising preliminary results, demonstrating a convenient, rapid (<20 min), quantitative, and sensitive (ng/mL) antigen/antibody assay. This integrated pre-screening model and simultaneous antigen/antibody approach may significantly improve accuracy of COVID-19 infection and host immunity screening, helping address unmet needs for monitoring vaccine effectiveness and severe disease surveillance.

Funder

Renaissance Health Service Corporation and Delta Dental of Michigan

NIH

Publisher

MDPI AG

Subject

Bioengineering

Reference53 articles.

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2. Safety and Efficacy of the MRNA BNT162b2 Vaccine against SARS-CoV-2 in Five Groups of Immunocompromised Patients and Healthy Controls in a Prospective Open-Label Clinical Trial;Bergman;eBioMedicine,2021

3. Duration of Effectiveness of Vaccines against SARS-CoV-2 Infection and COVID-19 Disease: Results of a Systematic Review and Meta-Regression;Feikin;Lancet,2022

4. (2023, March 01). CDC SARS-CoV-2 Variant Classifications and Definitions, Available online: https://www.cdc.gov/coronavirus/2019-ncov/variants/variant-classifications.html.

5. SARS-CoV-2 Omicron Strain Exhibits Potent Capabilities for Immune Evasion and Viral Entrance;Zhang;Signal Transduct. Target. Ther.,2021

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