Evidence map›Paper›PMID 35658040›Full record

ArticleScience advances2022

Microfluidic particle dam for direct visualization of SARS-CoV-2 antibody levels in COVID-19 vaccinees.

Minghui Wu, Siying Wu, Gaobo Wang, Wengang Liu, Lok Ting Chu, Tianyi Jiang, Hoi Kwan Kwong, Hiu Lam Chow, Iris Wai Sum Li, Ting-Hsuan Chen

Abstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Lab on an end: Micromanipulation using the acoustohydrodynamic pillar array as an end effector.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Minghui WuDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0002-1949-3349
Siying WuDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0003-0576-386X
Gaobo WangDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0002-4594-1635
Wengang LiuDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0003-3907-7702
Lok Ting ChuDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0002-6791-7468
Tianyi JiangDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0002-6939-607X
Hoi Kwan KwongDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0002-0542-6268
Hiu Lam ChowDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.
Iris Wai Sum LiHKU-Pasteur Research Pole, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.ORCID 0000-0001-7295-7432
Ting-Hsuan ChenDepartment of Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0003-4517-7750

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various COVID-19 vaccines are currently deployed, but their immunization varies and decays with time. Antibody level is a potent correlate to immune protection, but its quantitation relies on intensive laboratory techniques. Here, we report a decentralized, instrument-free microfluidic device that directly visualizes SARS-CoV-2 antibody levels. Magnetic microparticles (MMPs) and polystyrene microparticles (PMPs) can bind to SARS-CoV-2 antibodies simultaneously. In a microfluidic chip, this binding reduces the incidence of free PMPs escaping from magnetic separation and shortens PMP accumulation length at a particle dam. This visual quantitative result enables use in either sensitive mode [limit of detection (LOD): 13.3 ng/ml; sample-to-answer time: 70 min] or rapid mode (LOD: 57.8 ng/ml; sample-to-answer time: 20 min) and closely agrees with the gold standard enzyme-linked immunosorbent assay. Trials on 91 vaccinees revealed higher antibody levels in mRNA vaccinees than in inactivated vaccinees and their decay in 45 days, demonstrating the need for point-of-care devices to monitor immune protection.

Identifiers

PMID35658040
PMCPMC9166397

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.