Evidence map›Paper›PMID 25374821›Full record

ReviewWorld journal of nephrology2014

T-cell ageing in end-stage renal disease patients: Assessment and clinical relevance.

Ruud Wj Meijers, Michiel Gh Betjes, Carla C Baan, Nicolle Hr Litjens

Open access · hybridAbstract readReview
In one paragraph

Review in World journal of nephrology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Kidney Disease as a Driver of Immunosenescence: Mechanisms and Potential Interventions.Journal of the American Society of Nephrology : JASN · 2026
    Review
  6. Observational
  7. Observational
  8. Article
  9. Review
  10. Article
  11. Article
  12. Effects of bariatric surgery on telomere length and T-cell aging.International journal of obesity (2005) · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 1 institution in 1 country.

Ruud Wj MeijersRuud WJ Meijers, Michiel GH Betjes, Carla C Baan, Nicolle HR Litjens, Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Centre, 3000 CA Rotterdam, The Netherlands.
Michiel Gh BetjesRuud WJ Meijers, Michiel GH Betjes, Carla C Baan, Nicolle HR Litjens, Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Centre, 3000 CA Rotterdam, The Netherlands.
Carla C BaanRuud WJ Meijers, Michiel GH Betjes, Carla C Baan, Nicolle HR Litjens, Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Centre, 3000 CA Rotterdam, The Netherlands.
Nicolle Hr LitjensRuud WJ Meijers, Michiel GH Betjes, Carla C Baan, Nicolle HR Litjens, Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Centre, 3000 CA Rotterdam, The Netherlands.
Erasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

End-stage renal disease (ESRD) patients have a defective T-cell-mediated immune system which is related to excessive premature ageing of the T-cell compartment. This is likely to be caused by the uremia-associated pro-inflammatory milieu, created by loss of renal function. Therefore, ESRD patients are highly susceptible for infections, have an increased risk for virus-associated cancers, respond poorly to vaccination and have an increased risk for atherosclerotic diseases. Three ageing parameters can be used to assess an immunological T-cell age. First, thymic output can be determined by assessing the T-cell receptor excision circles-content together with CD31 expression within the naïve T cells. Second, the telomere length of T cells and third the T-cell differentiation status are also indicators of T-cell ageing. Analyses based on these parameters in ESRD patients revealed that the immunological T-cell age is increased by on average 20 years compared to the chronological age. After kidney transplantation (KTx) the aged T-cell phenotype persists although the pro-inflammatory milieu is diminished. This might be explained by epigenetic modifications at hematopoietic stem cells level. Assessment of an immunological T-cell age could be an important tool to identify KTx recipients who are at risk for allograft rejection or to prevent over-immunosuppression.

Indexed as

End-stage renal disease patientsKidney transplantationT-cell ageingT-cell differentiationUremia

Identifiers

PMID25374821
PMCPMC4220360
OpenAlexW2126094497

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.