Evidence map›Paper›PMID 34346525›Full record

ArticleJournal of leukocyte biology2022

Differential expression and regulation of MS4A family members in myeloid cells in physiological and pathological conditions.

Rita Silva-Gomes, Sarah N Mapelli, Marie-Astrid Boutet, Irene Mattiola, Marina Sironi, Fabio Grizzi, Federico Colombo, Domenico Supino, Silvia Carnevale, Fabio Pasqualini and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.8field-weighted citation impact, top 1% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Tissue signatures of human macrophages during homeostasis and activation.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Synovial MS4A4A correlates with inflammation and counteracts response to corticosteroids in arthritis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Ms4a4a deficiency ameliorates plaque pathology in a mouse model of amyloid accumulation.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Identifying MS4A6AHeliyon · 2024
    Article
  19. Article
  20. Hepatic danger signaling triggers TREM2Science translational medicine · 2024
    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

18 authors at 9 institutions in 5 countries.

Rita Silva-GomesDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Sarah N MapelliIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Marie-Astrid BoutetCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute and Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Irene MattiolaLaboratory of Innate Immunity, Department of Microbiology, Infectious Diseases and Immunology, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.
Marina SironiIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Fabio GrizziIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Federico ColomboIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Domenico SupinoDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Silvia CarnevaleDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Fabio PasqualiniDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Matteo StravalaciIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Rémi PorteIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Andrea GianattiUnit of Pathology, Azienda Ospedaliera Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Constantino PitzalisCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute and Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Massimo LocatiIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Maria José OliveiraICBAS-Institute of Biomedical Sciences Abel Salazar, University of Porto, Porto, Portugal.
Barbara BottazziIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Alberto MantovaniDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
IRCCS Humanitas Research Hospital · ITHumanitas University · ITQueen Mary University of London · GBBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DECentre National de la Recherche Scientifique · FRi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTOniris · FROspedale Papa Giovanni XXIII · ITUniversidade do Porto · PT

Funding

Versus Arthritis 21890
6 · The paper itself

Abstract

The MS4A gene family encodes 18 tetraspanin-like proteins, most of which with unknown function. MS4A1 (CD20), MS4A2 (FcεRIβ), MS4A3 (HTm4), and MS4A4A play important roles in immunity, whereas expression and function of other members of the family are unknown. The present investigation was designed to obtain an expression fingerprint of MS4A family members, using bioinformatics analysis of public databases, RT-PCR, and protein analysis when possible. MS4A3, MS4A4A, MS4A4E, MS4A6A, MS4A7, and MS4A14 were expressed by myeloid cells. MS4A6A and MS4A14 were expressed in circulating monocytes and decreased during monocyte-to-Mϕ differentiation in parallel with an increase in MS4A4A expression. Analysis of gene expression regulation revealed a strong induction of MS4A4A, MS4A6A, MS4A7, and MS4A4E by glucocorticoid hormones. Consistently with in vitro findings, MS4A4A and MS4A7 were expressed in tissue Mϕs from COVID-19 and rheumatoid arthritis patients. Interestingly, MS4A3, selectively expressed in myeloid precursors, was found to be a marker of immature circulating neutrophils, a cellular population associated to COVID-19 severe disease. The results reported here show that members of the MS4A family are differentially expressed and regulated during myelomonocytic differentiation, and call for assessment of their functional role and value as therapeutic targets.

Indexed as

COVID-19Membrane ProteinsAntigens, CD20FamilyHumansMonocytesAntigens, CD20Membrane ProteinsCOVID-19monocytes/MϕsMS4A3MS4A4AMS4A6Arheumatoid arthritis

Identifiers

PMID34346525
PMCPMC9290968
OpenAlexW3189583506

What OpenQuestion holds

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LicenceCC BY
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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.