Evidence map›Paper›PMID 35959245›Full record

ArticleSAGE open medicine2022

A rapid, easy, and scalable whole blood monocyte CD169 assay for outpatient screening during SARS-CoV-2 outbreak, and potentially other emerging disease outbreaks.

Moïse Michel, Fabrice Malergue, Inès Ait Belkacem, Pénélope Bourgoin, Pierre-Emmanuel Morange, Isabelle Arnoux, Tewfik Miloud, Matthieu Million, Hervé Tissot-Dupont, Jean-Louis Mege and 2 more

Open access · goldAbstract read
In one paragraph

Article in SAGE open medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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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

12 authors at 3 institutions in 1 country.

Moïse MichelAix-Marseille University, Marseille, France.ORCID https://orcid.org/0000-0002-0460-9898
Fabrice MalergueBeckman Coulter Life Sciences, Marseille, France.ORCID https://orcid.org/0000-0003-1322-1390
Inès Ait BelkacemBeckman Coulter Life Sciences, Marseille, France.
Pénélope BourgoinBeckman Coulter Life Sciences, Marseille, France.
Pierre-Emmanuel MorangeAPHM Hôpitaux Universitaires de Marseille, Hôpital Timone, Marseille, France.
Isabelle ArnouxAPHM Hôpitaux Universitaires de Marseille, Hôpital Timone, Marseille, France.
Tewfik MiloudBeckman Coulter Life Sciences, Marseille, France.
Matthieu MillionAPHM Hôpitaux Universitaires de Marseille, Hôpital Timone, Marseille, France.
Hervé Tissot-DupontAPHM Hôpitaux Universitaires de Marseille, Hôpital Timone, Marseille, France.ORCID https://orcid.org/0000-0002-6745-4360
Jean-Louis MegeAix-Marseille University, Marseille, France.
Joana VitteAix-Marseille University, Marseille, France.
Jean-Marc BusnelBeckman Coulter Life Sciences, Marseille, France.
Aix-Marseille Université · FRHôpital de la Timone · FRMéditerranée Infection Foundation · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The COVID-19 corona virus disease outbreak is globally challenging health systems and societies. Its diagnosis relies on molecular methods, with drawbacks revealed by mass screening. Upregulation of neutrophil CD64 or monocyte CD169 has been abundantly reported as markers of bacterial or acute viral infection, respectively. We evaluated the sensitivity of an easy, one-step whole blood flow cytometry assay to measure these markers within 10 min, as a potential screening test for COVID-19 patients. Methods: Patients ( Results: We observed 98% and 100% sensitivity in early-stage ( Conclusion: Monocyte CD169 evaluation was highly sensitive for detecting SARS-CoV-2 infection in first-presentation patients; and it returns to basal level upon infection clearance. The potential ease of fingerprick collection, minimal time-to-result, and low cost rank this biomarker measurement as a potential viral disease screening tool, including COVID-19. When the virus prevalence in the tested population is usually low (1%-10%), such an approach could increase the testing capacity 10 to 100-fold, with the same limited molecular testing resources, which could focus on confirmation purposes only.

Indexed as

CD169CD64COVID-19emerging diseaseflow cytometrymonocytesneutrophilsoutbreakSARS-CoV-2screening test

Identifiers

PMID35959245
PMCPMC9358337
OpenAlexW4289551869

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.