Evidence map›Paper›PMID 26188489›Full record

ReviewClinical and experimental medicine2016

T cell senescence and cardiovascular diseases.

Hee Tae Yu, Sungha Park, Eui-Cheol Shin, Won-Woo Lee

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Clinical and experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

56 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. CD31Physiological reports · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Advances in the study of the glymphatic system and aging.CNS neuroscience & therapeutics · 2024
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. The Aging Heart: A Molecular and Clinical Challenge.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Targeting Immune Senescence in Atherosclerosis.International journal of molecular sciences · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. Characteristics, outcomes, and predictors ofFrontiers in cardiovascular medicine · 2022
    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

4 authors at 3 institutions in 1 country.

Hee Tae YuLaboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Korea.
Sungha ParkDivision of Cardiology, Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.
Eui-Cheol ShinLaboratory of Immunology and Infectious Diseases, Graduate School of Medical Science and Engineering, KAIST, Daejeon, Korea. ecshin@kaist.ac.kr.
Won-Woo LeeDepartment of Biomedical Sciences and Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea. wonwoolee@snu.ac.kr.
Yonsei University · KRKorea Advanced Institute of Science and Technology · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related changes in the immune system, commonly termed "immunosenescence," contribute to deterioration of the immune response and fundamentally impact the health and survival of elderly individuals. Immunosenescence affects both the innate and adaptive immune systems; however, the most notable changes are in T cell immunity and include thymic involution, the collapse of T cell receptor (TCR) diversity, an imbalance in T cell populations, and the clonal expansion of senescent T cells. Senescent T cells have the ability to produce large quantities of proinflammatory cytokines and cytotoxic mediators; thus, they have been implicated in the pathogenesis of many chronic inflammatory diseases. Recently, an increasing body of evidence has suggested that senescent T cells also have pathogenic potential in cardiovascular diseases, such as hypertension, atherosclerosis, and myocardial infarction, underscoring the detrimental roles of these cells in various chronic inflammatory responses. Given that cardiovascular disease is the number one cause of death worldwide, there is great interest in understanding the contribution of age-related immunological changes to its pathogenesis. In this review, we discuss general features of age-related alterations in T cell immunity and the possible roles of senescent T cells in the pathogenesis of cardiovascular disease.

Indexed as

AgingAge FactorsCardiovascular DiseasesCytokinesHumansT-LymphocytesCytokinesCardiovascular disease (CVD)Cytomegalovirus (CMV)ImmunosenescenceInflammaging

Identifiers

PMID26188489
OpenAlexW2207430481

What OpenQuestion holds

Textmetadata
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.