Evidence map›Paper›PMID 40847483›Full record

ArticleJournal of the American Heart Association2025

Circulating Mucosal-Associated Invariant T Cells Are Associated With Acute Human Ischemic Stroke and Predict Poor Outcome.

Tadashi Ozawa, Asako Chiba, Hiroko Hayakawa, Tsukasa Ohmori, Sachiko Miyake, Shigeru Fujimoto, Ryota Tanaka

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Tadashi OzawaDivision of Neurology, Department of Medicine Jichi Medical University School of Medicine Tochigi Japan.ORCID 0000-0001-8050-7351
Asako ChibaDepartment of Immunology Juntendo University Graduate School of Medicine Tokyo Japan.
Hiroko HayakawaDepartment of Biochemistry, School of Medicine Jichi Medical University Tochigi Japan.
Tsukasa OhmoriDepartment of Biochemistry, School of Medicine Jichi Medical University Tochigi Japan.ORCID 0000-0001-5082-6394
Sachiko MiyakeDepartment of Immunology Juntendo University Graduate School of Medicine Tokyo Japan.
Shigeru FujimotoDivision of Neurology, Department of Medicine Jichi Medical University School of Medicine Tochigi Japan.ORCID 0000-0002-6295-4737
Ryota TanakaDivision of Neurology, Department of Medicine Jichi Medical University School of Medicine Tochigi Japan.ORCID 0000-0003-3158-1955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMucosal-associated invariant T (MAIT) cells are involved in acute ischemic stroke in mice models. This study aimed to clarify the dynamics and role of circulating MAIT cells in patients with acute ischemic stroke.

methodsPatients with acute ischemic stroke were classified according to the National Institutes of Health Stroke Scale into severe (score ≥ 10) and mild (score < 10) groups; outpatients with matched sex and age were selected as controls. Circulating MAIT cells, activation (CD69+), and cytokine production (IFN-γ [interferon-gamma] + and IL-17 [interleukin-17]+) on days 3, 10, and 17 after stroke, along with invariant natural killer T cells, gamma delta T cells, CD4+, and CD8+ T-cell populations, were analyzed by flow cytometry. The relationship between MAIT cell dynamics and clinical outcomes was examined.

resultsOne hundred participants (30 severe, 40 mild, 30 controls) were included. On day 3, patients with severe stroke had a significantly lower proportion of MAIT cells than the mild group and controls (severe, mild, control [median]: 0.09%, 0.33%, 0.38%, respectively;

conclusionsAn early decrease in MAIT cells with higher activity and proinflammatory cytokine production correlated with stroke severity and poor outcomes, suggesting a significant role of MAIT cells in acute cerebral infarction and unfavorable outcomes.

Indexed as

Ischemic StrokeMucosal-Associated Invariant T CellsAgedAntigens, CDAntigens, Differentiation, T-LymphocyteCase-Control StudiesCD69 AntigensFemaleFlow CytometryHumansInterferon-gammaInterleukin-17Lectins, C-TypeLymphocyte ActivationMaleMiddle AgedAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensInterferon-gammaInterleukin-17Lectins, C-Typegamma delta T cellsinvariant natural killer T cellischemic strokemucosal‐associated invariant T cellpoor outcome

Identifiers

PMID40847483
PMCPMC12553461

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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.