Evidence map›Paper›PMID 21214539›Full record

ArticleImmunology2011

Cytomegalovirus infection induces the accumulation of short-lived, multifunctional CD4+CD45RA+CD27+ T cells: the potential involvement of interleukin-7 in this process.

Valentina Libri, Rita I Azevedo, Sarah E Jackson, Diletta Di Mitri, Raskit Lachmann, Stephan Fuhrmann, Milica Vukmanovic-Stejic, Kwee Yong, Luca Battistini, Florian Kern and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 113 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Mapping CMV-related immune signatures in blood, aorta and perivascular mediastinal adipose tissue.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  7. CMV-specific clonal expansion of Th1, GZMKbioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Review
  10. Senescent T Cells: The Silent Culprit in Acute Myeloid Leukemia Progression?International journal of molecular sciences · 2024
    Review
  11. Review
  12. Article
  13. Article
  14. Proteostasis in T cell aging.Seminars in immunology · 2023
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

9 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

12 authors at 5 institutions in 4 countries.

Valentina LibriDivision of Infection and Immunity, University College London, London, UK.
Rita I Azevedo
Sarah E Jackson
Diletta Di Mitri
Raskit Lachmann
Stephan Fuhrmann
Milica Vukmanovic-Stejic
Kwee Yong
Luca Battistini
Florian Kern
Maria V D Soares
Arne N Akbar
University College London · GBBrighton and Sussex Medical School · GBEuropean Brain Research Institute · ITHelios Hospital Berlin-Buch · DEInstituto de Medicina Molecular João Lobo Antunes

Funding

Biotechnology and Biological Sciences Research Council BB/E019188/1
6 · The paper itself

Abstract

The relative roles that ageing and lifelong cytomegalovirus (CMV) infection have in shaping naive and memory CD4+ T-cell repertoires in healthy older people is unclear. Using multiple linear regression analysis we found that age itself is a stronger predictor than CMV seropositivity for the decrease in CD45RA+ CD27+ CD4+ T cells over time. In contrast, the increase in CD45RA⁻ CD27⁻ and CD45RA+ CD27⁻ CD4+ T cells is almost exclusively the result of CMV seropositivity, with age alone having no significant effect. Furthermore, the majority of the CD45RA⁻ CD27⁻ and CD45RA+ CD27⁻ CD4+ T cells in CMV-seropositive donors are specific for this virus. CD45RA+ CD27⁻ CD4+ T cells have significantly reduced CD28, interleukin-7 receptor α (IL-7Rα) and Bcl-2 expression, Akt (ser473) phosphorylation and reduced ability to survive after T-cell receptor activation compared with the other T-cell subsets in the same donors. Despite this, the CD45RA+ CD27⁻ subset is as multifunctional as the CD45RA⁻ D27+ and CD45RA⁻ CD27⁻ CD4+ T-cell subsets, indicating that they are not an exhausted population. In addition, CD45RA+ CD27⁻ CD4+ T cells have cytotoxic potential as they express high levels of granzyme B and perforin. CD4+ memory T cells re-expressing CD45RA can be generated from the CD45RA⁻ CD27+ population by the addition of IL-7 and during this process these cells down-regulated expression of IL-7R and Bcl-2 and so resemble their counterparts in vivo. Finally we showed that the proportion of CD45RA+ CD27⁻ CD4+ T cells of multiple specificities was significantly higher in the bone marrow than the blood of the same individuals, suggesting that this may be a site where these cells are generated.

Indexed as

AdultAgedAged, 80 and overAgingCD4-Positive T-LymphocytesCell DifferentiationCell SeparationCell SurvivalCytomegalovirus InfectionsFlow CytometryHumansInterleukin-7Leukocyte Common AntigensMiddle AgedSignal TransductionT-Lymphocyte SubsetsInterleukin-7Leukocyte Common AntigensTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID21214539
PMCPMC3044899
OpenAlexW1942062259

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.