Evidence map›Paper›PMID 38820600›Full record

ArticleAdvanced healthcare materials2025

Integrated Antigenic and Nucleic Acid Detection in Single Virions and Extracellular Vesicles with Viral Content.

Kim Truc Nguyen, Xilal Y Rima, Luong T H Nguyen, Xinyu Wang, Kwang Joo Kwak, Min Jin Yoon, Hong Li, Chi-Ling Chiang, Jacob Doon-Ralls, Kelsey Scherler and 15 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

25 authors.

Kim Truc NguyenWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Xilal Y RimaWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Luong T H NguyenWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Xinyu WangWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Kwang Joo KwakSpot Biosystems Ltd., Palo Alto, CA, 94301, USA.
Min Jin YoonWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Hong LiWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Chi-Ling ChiangWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Jacob Doon-RallsWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Kelsey ScherlerInstitute for Systems Biology, Seattle, WA, 98109, USA.
Shannon FallenInstitute for Systems Biology, Seattle, WA, 98109, USA.
Stephanie L GodfreyProvidence Swedish Medical Center, Seattle, WA, 98104, USA.
Julie A WallickProvidence Swedish Medical Center, Seattle, WA, 98104, USA.
Setty M MagañaTranslational Neuroimmunology, Center for Clinical and Translational Research, Nationwide Children's Hospital, Columbus, OH, 43205, USA.
Andre F PalmerWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Inyoul LeeInstitute for Systems Biology, Seattle, WA, 98109, USA.
Christopher C NunnProvidence Swedish Medical Center, Seattle, WA, 98104, USA.
Kimberly M ReevesProvidence Swedish Cancer Institute, Seattle, WA, 98104, USA.
Henry G KaplanProvidence Swedish Cancer Institute, Seattle, WA, 98104, USA.
Jason D GoldmanProvidence Swedish Medical Center, Seattle, WA, 98104, USA.
James R HeathInstitute for Systems Biology, Seattle, WA, 98109, USA.
Kai WangInstitute for Systems Biology, Seattle, WA, 98109, USA.
Preeti PancholiDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, 43203, USA.
L James LeeWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Eduardo ReáteguiWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.ORCID 0000-0002-8271-8205

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Multi-parametric Integrated Molecular Detection of SARS-CoV-2 from Biofluids by Adapting Single Extracellular Vesicle Characterization TechnologiesU18TR003807 · NCATS · OHIO STATE UNIVERSITY · PI LEE, INYOUL, LEE, LY JAMES · 2021 to 2022
$1.8M
Microfluidics Array Based Sorting, Isolation, and RNA Analysis in Single Extracellular V csiclesUH3TR002884 · NCATS · OHIO STATE UNIVERSITY · PI KIM, BETTY, REATEGUI, EDUARDO · 2021 to 2022
$1.7M
Microfluidics Array Based Sorting, Isolation, and RNA Analysis in Single Extracellular V csiclesUG3TR002884 · NCATS · OHIO STATE UNIVERSITY · PI KIM, BETTY, REATEGUI, EDUARDO · 2019 to 2020
$822k
Biomedical Advanced Research and Development HHSO10201600031CKaplan Cancer Research FundMerck and the Biomedical Advanced Research and Development Authority HHSO10201600031CNational Cancer Institute (NCI) subsidized Shared Resource P30CA016058National Institutes of Health (NIH) U18TR003807National Institutes of Health (NIH) UG3/UH3TR002884NCATS NIH HHS U18 TR003807NCATS NIH HHS UG3 TR002884NCATS NIH HHS UH3 TR002884NCI NIH HHS P30 CA016058The Murdock TrustThe Parker Institute for Cancer ImmunotherapyThe Swedish Medical Center FoundationU.S. Department of Defense W911NF-17-2-0086Wilke Family Foundation
6 · The paper itself

Abstract

Virion-mediated outbreaks are imminent and despite rapid responses, continue to cause adverse symptoms and death. Therefore, tunable, sensitive, high-throughput assays are needed to help diagnose future virion-mediated outbreaks. Herein, it is developed a tunable in situ assay to selectively enrich virions and extracellular vesicles (EVs) and simultaneously detect antigens and nucleic acids at a single-particle resolution. The Biochip Antigen and RNA Assay (BARA) enhanced sensitivities compared to quantitative reverse-transcription polymerase chain reaction (qRT-PCR), enabling the detection of virions in asymptomatic patients, genetic mutations in single virions, and enabling the continued long-term expression of viral RNA in the EV-enriched subpopulation in the plasma of patients with post-acute sequelae of the coronavirus disease of 2019 (COVID-19). BARA revealed highly accurate diagnoses of COVID-19 by simultaneously detecting the spike glycoprotein and nucleocapsid-encoding RNA in saliva and nasopharyngeal swab samples. Altogether, the single-particle detection of antigens and viral RNA provides a tunable framework for the diagnosis, monitoring, and mutation screening of current and future outbreaks.

Indexed as

Antigens, ViralCOVID-19Extracellular VesiclesRNA, ViralSARS-CoV-2VirionHumansSalivaSpike Glycoprotein, CoronavirusAntigens, ViralRNA, ViralSpike Glycoprotein, CoronavirusCOVID‐19, multiparametricSARS‐CoV‐2single extracellular vesiclesingle virion

Identifiers

PMID38820600
PMCPMC11773111

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.