Evidence map›Paper›PMID 38727285›Full record

ReviewCells2024

CD4

Yan Gao, Yaoping Lu, Xiaojing Liang, Mengwei Zhao, Xinyue Yu, Haiying Fu, Wei Yang

Abstract readReview
In one paragraph

Review in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Review
  3. CD8Science China. Life sciences · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Comparison of BeiyiFrontiers in pharmacology · 2026
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Immunosenescence: signaling pathways, diseases and therapeutic targets.Signal transduction and targeted therapy · 2025
    Review
  16. Review
  17. Review
  18. The progress of the microbe-gut-brain axis in sepsis-associated encephalopathy.Frontiers in cellular and infection microbiology · 2025
    Review
  19. 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.

Yan GaoDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Yaoping LuDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Xiaojing LiangDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Mengwei ZhaoDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Xinyue YuDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Haiying FuDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.ORCID 0000-0002-9878-0089
Wei YangDepartment of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.

Funding

Jilin Province Science and Technology Department 20230505039ZP
6 · The paper itself

Abstract

With the increasing proportion of the aging population, neurodegenerative diseases have become one of the major health issues in society. Neurodegenerative diseases (NDs), including multiple sclerosis (MS), Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS), are characterized by progressive neurodegeneration associated with aging, leading to a gradual decline in cognitive, emotional, and motor functions in patients. The process of aging is a normal physiological process in human life and is accompanied by the aging of the immune system, which is known as immunosenescence. T-cells are an important part of the immune system, and their senescence is the main feature of immunosenescence. The appearance of senescent T-cells has been shown to potentially lead to chronic inflammation and tissue damage, with some studies indicating a direct link between T-cell senescence, inflammation, and neuronal damage. The role of these subsets with different functions in NDs is still under debate. A growing body of evidence suggests that in people with a ND, there is a prevalence of CD4

Indexed as

CD4-Positive T-LymphocytesNeurodegenerative DiseasesT-Cell SenescenceAgingAnimalsHumansCD4+ T-cellsimmunosenescenceneurodegenerative diseasetherapy

Identifiers

PMID38727285
PMCPMC11083511

What OpenQuestion holds

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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.