# A Novel Flow Cytometry Array for High Throughput Detection of SARS-CoV-2 Antibodies

**Authors:** Benyue Zhang, Zhuo Zhang, Yichao Zhao, Jingqiao Lu, Jianmin Fang, Brianne Petritis, Kelly Whittaker, Rani Huang, Ruo-Pan Huang

PMC · DOI: 10.3390/vaccines13101063 · Vaccines · 2025-10-17

## TL;DR

A new flow cytometry method detects SARS-CoV-2 antibodies quickly and reliably, making it useful for large-scale studies.

## Contribution

A novel multiplex bead-based assay for high-throughput detection of SARS-CoV-2 antibodies with high reproducibility.

## Key findings

- The assay measured three antibody types in 624 samples within 2 hours.
- Intra- and inter-plate coefficients of variation were low, indicating high reproducibility.
- The platform effectively quantified background noise for easier data interpretation.

## Abstract

Background/Objectives: Although the U.S. Food and Drug Administration (FDA) has approved one antiviral treatment and authorized others for emergency use, there is no fully effective antiviral therapy for coronavirus disease 2019 (COVID-19), which is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Assays detecting virus-specific immunoglobulins (Ig) or nucleic acids in large-scale epidemiological, vaccine, and drug development studies remain limited due to high costs, reagent accessibility, and cumbersome protocols. Methods: A multiplex bead-based assay was developed to simultaneously detect human IgM, IgG, and IgA antibodies against the SARS-CoV-2 spike receptor binding domain (RBD) in serum using flow cytometry. Assay performance was evaluated for sensitivity, specificity, reproducibility, and cross-reactivity and compared to another immunoassay platform. Results: The assay enabled simultaneous measurement of three antibody isotypes across 624 samples within 2 h. Intra-plate coefficients of variation (CVs) ranged from 3.16 to 6.71%, and inter-plate CVs ranged from 3.33 to 5.49%, demonstrating high reproducibility. The platform also quantified background noise from nonspecific binding, facilitating straightforward data interpretation. Conclusions: This novel, flexible multiplex bead-based assay utilizing a well-established platform provides a rapid and reproducible approach for detecting SARS-CoV-2-specific antibodies. Its high throughput capacity and low variability make it well suited for large-scale epidemiological, vaccine, and therapeutic studies. The platform’s adaptability further supports application to other infectious diseases, offering an ideal tool for broad immunological surveillance.

## Linked entities

- **Diseases:** coronavirus disease 2019 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** infectious diseases (MESH:D003141), COVID-19 (MESH:D000086382)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12567774/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12567774/full.md

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Source: https://tomesphere.com/paper/PMC12567774