Evidence map›Paper›PMID 34335623›Full record

ReviewFrontiers in immunology2021

T Cell Response in Ischemic Stroke: From Mechanisms to Translational Insights.

Dianhui Zhang, Jiaxin Ren, Yun Luo, Qianyan He, Ruoyu Zhao, Junlei Chang, Yi Yang, Zhen-Ni Guo

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

78 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
  2. Article
  3. The kallikrein-kinin system modulates CD4Journal of neuroinflammation · 2026
    Article
  4. Review
  5. Review
  6. Lipid metabolism, microglia, and stroke.Neural regeneration research · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

18 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 1 country.

Dianhui ZhangStroke Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
Jiaxin RenStroke Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
Yun LuoStroke Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
Qianyan HeStroke Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
Ruoyu ZhaoStroke Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
Junlei ChangShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Yi YangStroke Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
Zhen-Ni GuoNeuroscience Center, Department of Neurology, First Affiliated Hospital of Jilin University, Changchun, China.
First Hospital of Jilin University · CNJilin University · CNChinese Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic stroke, caused by a sudden disruption of blood flow to the brain, is a leading cause of death and exerts a heavy burden on both patients and public health systems. Currently available treatments for ischemic stroke are very limited and are not feasible in many patients due to strict time windows required for their administration. Thus, novel treatment strategies are keenly required. T cells, which are part of the adaptive immune system, have gained more attention for its effects in ischemic stroke. Both preclinical and clinical studies have revealed the conflicting roles for T cells in post-stroke inflammation and as potential therapeutic targets. This review summarizes the mediators of T cell recruitment, as well as the temporal course of its infiltration through the blood-brain-barrier, choroid plexus, and meningeal pathways. Furthermore, we describe the mechanisms behind the deleterious and beneficial effects of T cells in the brain, in both antigen-dependent and antigen-independent manners, and finally we specifically focus on clinical and preclinical studies that have investigated T cells as potential therapeutic targets for ischemic stroke.

Indexed as

AnimalsHumansInflammationIschemic StrokeT-Lymphocytesimmune responsesischemic strokepost-stroke inflammationstroke therapyT cells

Identifiers

PMID34335623
PMCPMC8320432
OpenAlexW3183539318

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.