4.4 Article

Single-Dilution COVID-19 Antibody Test with Qualitative and Quantitative Readouts

Journal

MSPHERE
Volume 6, Issue 2, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/mSphere.00224-21

Keywords

COVID-19; IgA; IgG; laboratory diagnostic test; quantitative test; SARS-CoV-2; serology; spike protein

Categories

Funding

  1. National Institutes of Health [AI132633, AI125462, AI23654, AI143153, 3UL1TR002556-04S1, AI124753, AI13261, AI134753, AI145024]
  2. COVID-19 pilot award from the Albert Einstein College of Medicine
  3. NRC Research Associateship award
  4. G. Harold and Leila Y. Mathers Charitable Foundation
  5. Pew Charitable Trusts
  6. NIH at the Albert Einstein College of Medicine [2T32GM007288-45]
  7. EinsteinRockefellerCUNY Center for AIDS Research [P30AI124414]

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The article describes a laboratory-developed antibody test for detecting SARS-CoV-2 exposure with high sensitivity and specificity. The test can estimate viral spike-specific IgG titers and provide a scalable method to measure individual immune response strength. The ELISA-based serology test developed in the study can help guide patient care plans and public health policies, and is relatively easy to deploy.
The coronavirus disease 2019 (COVID-19) global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to place an immense burden on societies and health care systems. A key component of COVID-19 control efforts is serological testing to determine the community prevalence of SARS-CoV-2 exposure and quantify individual immune responses to prior SARS-CoV-2 infection or vaccination. Here, we describe a laboratory-developed antibody test that uses readily available research-grade reagents to detect SARS-CoV-2 exposure in patient blood samples with high sensitivity and specificity. We further show that this sensitive test affords the estimation of viral spike-specific IgG titers from a single sample measurement, thereby providing a simple and scalable method to measure the strength of an individual's immune response. The accuracy, adaptability, and cost-effectiveness of this test make it an excellent option for clinical deployment in the ongoing COVID-19 pandemic. IMPORTANCE Serological surveillance has become an important public health tool during the COVID-19 pandemic. Detection of protective antibodies and seroconversion after SARS-CoV-2 infection or vaccination can help guide patient care plans and public health policies. Serology tests can detect antibodies against past infections; consequently, they can help overcome the shortcomings of molecular tests, which can detect only active infections. This is important, especially when considering that many COVID-19 patients are asymptomatic. In this study, we describe an enzyme-linked immunosorbent assay (ELISA)-based qualitative and quantitative serology test developed to measure IgG and IgA antibodies against the SARS-CoV-2 spike glycoprotein. The test can be deployed using commonly available laboratory reagents and equipment and displays high specificity and sensitivity. Furthermore, we demonstrate that IgG titers in patient samples can be estimated from a single measurement, enabling the assay's use in high-throughput clinical environments.

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