Evidence map›Paper›PMID 31080378›Full record

ArticleClinical proteomics2019

Quantitative proteomic analyses of CD4

Tone Berge, Anna Eriksson, Ina Skaara Brorson, Einar August Høgestøl, Pål Berg-Hansen, Anne Døskeland, Olav Mjaavatten, Steffan Daniel Bos, Hanne F Harbo, Frode Berven

Open access · goldAbstract read
In one paragraph

Article in Clinical proteomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Observational
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Proteomics in Multiple Sclerosis: The Perspective of the Clinician.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. The Loss of HLA-F/KIR3DS1 Ligation Is Mediated by Hemoglobin Peptides.International journal of molecular sciences · 2020
    Article
  15. Article
  16. Neuronal RNA-binding protein dysfunction in multiple sclerosis cortex.Annals of clinical and translational neurology · 2020
    Article
  17. Review
  18. Article
  19. Review
  20. 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

10 authors at 2 institutions in 2 countries.

Tone BergeDepartment of Mechanical, Electronics and Chemical Engineering, Faculty of Technology, Art and Design, Oslo Met - Oslo Metropolitan University, Postboks 4, St. Olavs Plass, 0130 Oslo, Norway.ORCID 0000-0002-5297-2034
Anna Eriksson2Neuroscience Research Unit, Oslo University Hospital, Rikshospitalet, Domus Medica 4, Nydalen, Postboks 4950, 0424 Oslo, Norway.
Ina Skaara Brorson2Neuroscience Research Unit, Oslo University Hospital, Rikshospitalet, Domus Medica 4, Nydalen, Postboks 4950, 0424 Oslo, Norway.
Einar August Høgestøl2Neuroscience Research Unit, Oslo University Hospital, Rikshospitalet, Domus Medica 4, Nydalen, Postboks 4950, 0424 Oslo, Norway.
Pål Berg-Hansen4Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Anne Døskeland6Proteomics Unit at University of Bergen (PROBE), Department of Biomedicine, University of Bergen, Postboks 7804, 5020 Bergen, Norway.
Olav Mjaavatten6Proteomics Unit at University of Bergen (PROBE), Department of Biomedicine, University of Bergen, Postboks 7804, 5020 Bergen, Norway.
Steffan Daniel Bos2Neuroscience Research Unit, Oslo University Hospital, Rikshospitalet, Domus Medica 4, Nydalen, Postboks 4950, 0424 Oslo, Norway.
Hanne F Harbo4Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Frode Berven6Proteomics Unit at University of Bergen (PROBE), Department of Biomedicine, University of Bergen, Postboks 7804, 5020 Bergen, Norway.
Oslo University Hospital · NOUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple sclerosis (MS) is an autoimmune, neuroinflammatory disease, with an unclear etiology. However, T cells play a central role in the pathogenesis by crossing the blood-brain-barrier, leading to inflammation of the central nervous system and demyelination of the protective sheath surrounding the nerve fibers. MS has a complex inheritance pattern, and several studies indicate that gene interactions with environmental factors contribute to disease onset.

methodsIn the current study, we evaluated T cell dysregulation at the protein level using electrospray liquid chromatography-tandem mass spectrometry to get novel insights into immune-cell processes in MS. We have analyzed the proteomic profiles of CD4

resultsAn overall higher protein abundance was observed in both CD4

conclusionOur study provides evidence for proteomic differences in T cells from relapsing-remitting MS patients compared to healthy controls and also identifies dysregulation of proteins encoded from MS susceptibility genes.

Indexed as

AutoimmunityMass spectrometryMultiple sclerosisProteomicsSNPsT cells

Identifiers

PMID31080378
PMCPMC6505067
OpenAlexW2947944689

What OpenQuestion holds

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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.