Evidence map›Paper›PMID 27073295›Full record

ArticleMediators of inflammation2016

Reduced Numbers and Impaired Function of Regulatory T Cells in Peripheral Blood of Ischemic Stroke Patients.

Johanna Ruhnau, Juliane Schulze, Bettina von Sarnowski, Marie Heinrich, Sönke Langner, Christian Pötschke, Anika Wilden, Christof Kessler, Barbara M Bröker, Antje Vogelgesang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

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  15. Article
  16. Inflammatory Responses After Ischemic Stroke.Seminars in immunopathology · 2022
    Review
  17. Article
  18. Regulatory T cells in ischemic stroke.CNS neuroscience & therapeutics · 2021
    Review
  19. Article
  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

11 authors at 1 institution in 1 country.

Johanna RuhnauDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.
Juliane SchulzeDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.
Bettina von SarnowskiDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.
Marie HeinrichDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.
Sönke LangnerDepartment of Diagnostic Radiology and Neuroradiology, University Medicine Greifswald, 17475 Greifswald, Germany.
Christian PötschkeDepartment of Immunology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0003-0302-1811
Anika WildenDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.
Christof KesslerDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.
Barbara M BrökerDepartment of Immunology, University Medicine Greifswald, 17475 Greifswald, Germany.
Antje VogelgesangDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0003-2984-0831
Alexander DresselDepartment of Neurology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-9055-4327
Universitätsmedizin Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeRegulatory T cells (Tregs) have been suggested to modulate stroke-induced immune responses. However, analyses of Tregs in patients and in experimental stroke have yielded contradictory findings. We performed the current study to assess the regulation and function of Tregs in peripheral blood of stroke patients. Age dependent expression of CD39 on Tregs was quantified in mice and men.

methodsTotal FoxP3(+) Tregs and CD39(+)FoxP3(+) Tregs were quantified by flow cytometry in controls and stroke patients on admission and on days 1, 3, 5, and 7 thereafter. Treg function was assessed by quantifying the inhibition of activation-induced expression of CD69 and CD154 on T effector cells (Teffs).

resultsTotal Tregs accounted for 5.0% of CD4(+) T cells in controls and <2.8% in stroke patients on admission. They remained below control values until day 7. CD39(+) Tregs were most strongly reduced in stroke patients. On day 3 the Treg-mediated inhibition of CD154 upregulation on CD4(+) Teff was impaired in stroke patients. CD39 expression on Treg increased with age in peripheral blood of mice and men.

conclusionWe demonstrate a loss of active FoxP3(+)CD39(+) Tregs from stroke patient's peripheral blood. The suppressive Treg function of remaining Tregs is impaired after stroke.

Indexed as

AgedAged, 80 and overAnimalsAntigens, CDApyraseCD4-Positive T-LymphocytesFemaleForkhead Transcription FactorsHumansMaleMiceMiddle AgedStrokeT-Lymphocytes, RegulatoryAntigens, CDApyraseCD39 antigenForkhead Transcription FactorsFOXP3 protein, human

Identifiers

PMID27073295
PMCPMC4814689
OpenAlexW2300365585

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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.