Evidence map›Paper›PMID 28710491›Full record

ArticleScientific reports2017

Ageing and latent CMV infection impact on maturation, differentiation and exhaustion profiles of T-cell receptor gammadelta T-cells.

Martine J Kallemeijn, Anne Mieke H Boots, Michèle Y van der Klift, Elisabeth Brouwer, Wayel H Abdulahad, Jan A N Verhaar, Jacques J M van Dongen, Anton W Langerak

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Review
  3. Joining the dots: maternal cytomegalovirus, HIV and the placenta.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  4. The immune response to human cytomegalovirus: impact of age, co-morbidities and the significance of anti-viral activity assessment.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
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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

8 authors.

Martine J KallemeijnDepartment of Immunology, Laboratory for Medical Immunology, Erasmus MC, Rotterdam, 3000 CA, The Netherlands.
Anne Mieke H BootsDepartment of Rheumatology, University Medical Centre Groningen, Groningen, 9700 RB, The Netherlands.
Michèle Y van der KliftDepartment of Immunology, Laboratory for Medical Immunology, Erasmus MC, Rotterdam, 3000 CA, The Netherlands.
Elisabeth BrouwerDepartment of Rheumatology, University Medical Centre Groningen, Groningen, 9700 RB, The Netherlands.
Wayel H AbdulahadDepartment of Rheumatology, University Medical Centre Groningen, Groningen, 9700 RB, The Netherlands.
Jan A N VerhaarDepartment of Orthopedics, Erasmus MC, Rotterdam, 3000 CA, The Netherlands.
Jacques J M van DongenDepartment of Immunology, Laboratory for Medical Immunology, Erasmus MC, Rotterdam, 3000 CA, The Netherlands.
Anton W LangerakDepartment of Immunology, Laboratory for Medical Immunology, Erasmus MC, Rotterdam, 3000 CA, The Netherlands. a.langerak@erasmusmc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ageing is a broad cellular process, largely affecting the immune system, especially T-lymphocytes. Additionally to immunosenescence alone, cytomegalovirus (CMV) infection is thought to have major impacts on T-cell subset composition and exhaustion. These impacts have been studied extensively in TCRαβ+ T-cells, with reduction in naive, increase in effector (memory) subsets and shifts in CD4/CD8-ratios, in conjunction with morbidity and mortality in elderly. Effects of both ageing and CMV on the TCRγδ+ T-cell compartment remain largely elusive. In the current study we investigated Vγ- and Vδ-usage, maturation, differentiation and exhaustion marker profiles of both CD4 and CD8 double-negative (DN) and CD8+TCRγδ+ T-cells in 157 individuals, age range 20-95. We observed a progressive decrease in absolute numbers of total TCRγδ+ T-cells in blood, affecting the predominant Vγ9/Vδ2 population. Aged TCRγδ+ T-cells appeared to shift from naive to more (late-stage) effector phenotypes, which appeared more prominent in case of persistent CMV infections. In addition, we found effects of both ageing and CMV on the absolute counts of exhausted TCRγδ+ T-cells. Collectively, our data show a clear impact of ageing and CMV persistence on DN and CD8+TCRγδ+ T-cells, similar to what has been reported in CD8+TCRαβ+ T-cells, indicating that they undergo similar ageing processes.

Indexed as

AdultAgedAged, 80 and overAge DistributionAgingCase-Control StudiesCell DifferentiationCytomegalovirusCytomegalovirus InfectionsFemaleHumansMaleMiddle AgedReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsVirus LatencyReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID28710491
PMCPMC5511140

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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.