Evidence map›Paper›PMID 26190355›Full record

ReviewImmunology2015

The life (and death) of CD4+ CD28(null) T cells in inflammatory diseases.

Ingrid E Dumitriu

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04012294 (Effects of Allopurinol on Inflammatory Markers and Morphostructural Changes Evidenced by Musculoskeletal Ultrasound in Individuals With Asymptomatic Hyperuricemia. A Proof of Concept), which is not on this map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
4.2field-weighted citation impact, top 5% 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.

NCT04012294 phase3unknown statusnot on this mapstarted 2019, after this paper: background citation

Effects of Allopurinol on Inflammatory Markers and Morphostructural Changes Evidenced by Musculoskeletal Ultrasound in Individuals With Asymptomatic Hyperuricemia. A Proof of Concept

TypeinterventionalSponsorInstituto Nacional de Cardiologia Ignacio ChavezRan2019 to 2021Enrolled200ConditionsMusculoskeletal Degeneration, Inflammation, HyperuricemiaArmsAllopurinol Pill
3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 105 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Chronic Inflammation and Coronary Microvascular Dysfunction.Reviews in cardiovascular medicine · 2026
    Review
  4. Cytomegalovirus Drives the Development of Cytotoxic CD4Neurology(R) neuroimmunology & neuroinflammation · 2026
    Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Senescent CD4Clinical rheumatology · 2023
    Article
  18. Review
  19. Review
  20. Article

8 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

1 author at 1 institution in 1 country.

Ingrid E DumitriuCardiovascular and Cell Sciences Research Institute, St George's, University of London, London, UK.
St George's, University of London · GB

Funding

British Heart Foundation PG/10/50/28434British Heart Foundation PG/13/24/30115British Heart Foundation PG/14/18/30724
6 · The paper itself

Abstract

Inflammation contributes to the development and perpetuation of several disorders and T lymphocytes orchestrate the inflammatory immune response. Although the role of T cells in inflammation is widely recognized, specific therapies that tackle inflammatory networks in disease are yet to be developed. CD4(+) CD28(null) T cells are a unique subset of helper T lymphocytes that recently shot back into the limelight as potential catalysts of inflammation in several inflammatory disorders such as autoimmunity, atherosclerosis and chronic viral infections. In contrast to conventional helper T cells, CD4(+) CD28(null) T cells have an inbuilt ability to release inflammatory cytokines and cytotoxic molecules that can damage tissues and amplify inflammatory pathways. It comes as no surprise that patients who have high numbers of these cells have more severe disease and poor prognosis. In this review, I provide an overview on the latest advances in the biology of CD4(+) CD28(null) T cells. Understanding the complex functions and dynamics of CD4(+) CD28(null) T cells may open new avenues for therapeutic intervention to prevent progression of inflammatory diseases.

Indexed as

Cytotoxicity, ImmunologicAnimalsAnti-Inflammatory AgentsCD28 AntigensCell DeathCell ProliferationCytokinesHumansInflammationInflammation MediatorsLymphocyte ActivationPhenotypePrognosisSeverity of Illness IndexSignal TransductionT-Lymphocytes, Helper-InducerAnti-Inflammatory AgentsCD28 AntigensCytokinesInflammation MediatorsapoptosisatherosclerosisautoimmunityCD4+CD28null T lymphocytesco-stimulationhelper T cellsinflammation

Identifiers

PMID26190355
PMCPMC4582960
OpenAlexW2099253077

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.