# A Versatile High‐Throughput Single‐Cell Screening Platform for Profiling Antigen‐Specific Long‐Lived B Cells in Blood and Bone Marrow

**Authors:** Tian Zhao, Yuqing Lei, Chang Liu, Dong Zhang, Kaiyi Li, Sisi Shan, Chenyu Li, Zimeng Wei, Yuhan Yang, Ting Zhang, Kai Sun, Haoran Sun, Linqi Zhang, Peng Liu

PMC · DOI: 10.1002/advs.202414945 · Advanced Science · 2025-04-09

## TL;DR

A new high-throughput platform enables detailed study of B cells involved in long-term immunity, including those from vaccinated mice.

## Contribution

The MoSMAR-chip is a novel platform for profiling antigen-specific B cells at the single-cell level with high throughput and low cost.

## Key findings

- The MoSMAR-chip successfully analyzed ASCs from COVID-19 vaccine-immunized mice.
- Diverse neutralizing antibodies against the JN1 variant of SARS-CoV-2 were identified.
- The platform enables efficient multi-omics and functional analysis of antigen-specific B cells.

## Abstract

Antigen‐specific B cells play a crucial role in the long‐term immune response following infection or vaccination, differentiating into antibody‐secreting cells (ASCs) and memory B cells (MBCs). However, profiling ASCs is challenging primarily due to their lack of membrane‐bound surface B cell receptors. In this study, the Modular Superhydrophobic Microwell Array Chip (MoSMAR‐chip) is introduced as a versatile, cost‐effective, and high‐throughput platform for identifying and characterizing individual antigen‐specific ASCs and MBCs at the single‐cell level within seven days. Using this platform, comprehensive analyses of single ASCs could be performed from bone marrows of coronavirus disease 2019 (COVID‐19) vaccine‐immunized mice and a diverse set of antibodies capable of neutralizing the highly divergent JN1 variant of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) were identified. These results demonstrate that the MoSMAR‐chip facilitates efficient single‐cell multi‐omics and functional analyses of antigen‐specific ASCs, offering a powerful tool for investigating complex long‐term B cell immunity in diverse clinical conditions, such as infectious diseases, autoimmunity, and beyond.

The MoSMAR‐chip platform provides a high‐throughput and cost‐effective tool for identifying and characterizing antigen‐specific antibody‐secreting cells (ASCs) and memory B cells (MBCs) at the single‐cell level. The ASCs from coronavirus disease 2019 (COVID‐19) vaccine‐immunized mice were successfully analyzed, revealing diverse neutralizing antibodies against the JN1 variant. The platform enables efficient single‐cell multi‐omics and functional studies, advancing B cell immunity research.

## Linked entities

- **Diseases:** coronavirus disease 2019 (MONDO:0100096)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** COVID-19 (MESH:D000086382), infection (MESH:D007239), infectious diseases (MESH:D003141)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12140366/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12140366/full.md

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Source: https://tomesphere.com/paper/PMC12140366