Evidence map›Paper›PMID 35911740›Full record

ArticleFrontiers in immunology2022

Shinichi Yamamoto, Ako Matsui, Masaki Ohyagi, Chie Kikutake, Yoshihiro Harada, Mana Iizuka-Koga, Mikita Suyama, Akihiko Yoshimura, Minako Ito

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Targeting IL-33 in Precision Neuroimmunology: Cellular Mechanisms and Therapeutic Strategies for CNS Disorders.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Brain regulatory T cells.Nature reviews. Immunology · 2024
    Review
  7. Review
  8. Article
  9. Neuroinflammation in Acute Ischemic and Hemorrhagic Stroke.Current neurology and neuroscience reports · 2023
    Review
  10. Article
  11. 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

9 authors at 2 institutions in 1 country.

Shinichi YamamotoDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Ako MatsuiDivision of Allergy and Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Masaki OhyagiDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Chie KikutakeDivision of Bioinformatics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Yoshihiro HaradaDivision of Allergy and Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Mana Iizuka-KogaDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Mikita SuyamaDivision of Bioinformatics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Akihiko YoshimuraDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Minako ItoDivision of Allergy and Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Kyushu University · JPKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Tregs) are normally born in the thymus and activated in secondary lymphoid tissues to suppress immune responses in the lymph node and at sites of inflammation. Tregs are also resident in various tissues or accumulate in damaged tissues, which are now called tissue Tregs, and contribute to homeostasis and tissue repair by interacting with non-immune cells. We have shown that Tregs accumulate in the brain during the chronic phase in a mouse cerebral infarction model, and these Tregs acquire the characteristic properties of brain Tregs and contribute to the recovery of neurological damage by interacting with astrocytes. However, the mechanism of tissue Treg development is not fully understood. We developed a culture method that confers brain Treg characteristics

Indexed as

AstrocytesT-Lymphocytes, RegulatoryAnimalsBrainMiceReceptors, Antigen, T-CellReceptors, SerotoninReceptors, Antigen, T-CellReceptors, SerotoninastrocyteIL-33Parkinson’s diseaseserotonintissue Tregs

Identifiers

PMID35911740
PMCPMC9335882
OpenAlexW4285593002

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.