Evidence map›Paper›PMID 40628860›Full record

ArticleScientific reports2025

Changes in peripheral blood mononuclear cell electrical properties in response to viral exposure and vaccination.

Krista S P Clarke, Alexander T Stewart, Emma L Sinclair, Rebecca Lewis, Fatima H Labeed, Deborah K Dunn-Walters, Michael Pycraft Hughes

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Krista S P ClarkeCentre for Biomedical Engineering, School of Mechanical Engineering Sciences, University of Surrey, Guildford, Surrey, GU2 7XH, UK.
Alexander T StewartSchool of Bioscience and Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK.
Emma L SinclairSchool of Bioscience and Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK.
Rebecca LewisDepartment of Comparative Biomedical Sciences, School of Veterinary Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK.
Fatima H LabeedDepartment of Biology, United Arab Emirates University, Al Ain, UAE.
Deborah K Dunn-WaltersSchool of Bioscience and Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK. d.dunn-walters@surrey.ac.uk.
Michael Pycraft HughesDepartment of Biomedical Engineering and Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, UAE. michael.hughes@ku.ac.ae.

Funding

Biotechnology and Biological Sciences Research Council BB/T002212/1Deparator PhD studentshipKhalifa University of Science, Technology and Research FSU-2022-020
6 · The paper itself

Abstract

Viral infection triggers both cellular and systemic responses in vivo. These are sometimes difficult to study since the immune system is subject to constant challenge from multiple pathogens. However, during the COVID-19 pandemic, a unique opportunity arose to measure the body's immune response during lockdown, when exposure to pathogens from the environment was substantially lower. This allowed measurement of COVID-naïve patients, as well as those who had recovered from COVID-19. The effects of subsequent vaccination and boosters could also be assessed. This offers two advantages; an insight into the humoral response to novel pathogens, and the opportunity to measure the ability of the body to respond to challenge from both new pathogens and those to which exposure had already occurred. In this paper, we used dielectrophoresis (DEP) to analyze the electrophysiological fingerprint of peripheral blood mononuclear cells (PBMCs) from donors who had never had COVID-19, those who had recovered from COVID-19, and those who received first, second, or third vaccine doses. This was performed before and after incubation with the receptor binding domain of the SARS-CoV-2 spike protein to determine whether differential changes in the electrical properties of PBMCs could be detected and evaluated. Clear trends in response over time were observed, suggesting that DEP could pave the way towards a new correlate of protection (CoP) to SARS-CoV-2. Furthermore, since the test measures immune response to challenge, it may be widely applicable to other diseases.

Indexed as

COVID-19COVID-19 VaccinesLeukocytes, MononuclearSARS-CoV-2AdultFemaleHumansMaleMiddle AgedSpike Glycoprotein, CoronavirusVaccinationCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Correlate of protectionCytoplasmic conductivityDielectrophoresisMembrane capacitanceMembrane conductancePeripheral blood mononuclear cellSARS-CoV-2

Identifiers

PMID40628860
PMCPMC12238384

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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 Socratic graph.