Evidence map›Paper›PMID 20700658›Full record

ArticleAge (Dordrecht, Netherlands)2011

Age-related deregulation of naive T cell homeostasis in elderly humans.

Sara Ferrando-Martínez, Ezequiel Ruiz-Mateos, Ana Hernández, Encarnación Gutiérrez, Maria del Mar Rodríguez-Méndez, Antonio Ordoñez, Manuel Leal

Abstract read
In one paragraph

Article in Age (Dordrecht, Netherlands), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

48 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Frontiers in immunology · 2025
    Article
  9. Immunotherapy: should we worry about immunosenescence?Ageing and cancer research & treatment · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  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

7 authors at 3 institutions in 1 country.

Sara Ferrando-MartínezLaboratory of Immunovirology, Biomedicine Institute of Seville (IBIS). Service of Infectious Diseases, Virgen del Rocío University Hospital, Avda. Manuel Siurot s/n, 41013, Seville, Spain.
Ezequiel Ruiz-Mateos
Ana Hernández
Encarnación Gutiérrez
Maria del Mar Rodríguez-Méndez
Antonio Ordoñez
Manuel Leal
Hospital Universitario Virgen del Rocío · ESInstituto de Biomedicina de Sevilla · ESUniversidad de Sevilla · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunosenescence is characterized by phenotypic and functional changes of effector memory T cells. In spite of the well-described senescent defects of these experienced T cells, immune responses to new pathogens are also deeply affected in elderly humans, suggesting that naive T cells could also show age-related defects. It has been reported in both, animal models and humans, alterations of the naive T cell turnover associated to advanced age or low thymic function. However, as far as we know, homeostatic mechanisms involved in the deregulation of naive T cell peripheral dynamics and their consequences are still not well understood. Thus, the aim of our study was to analyze homeostatic parameters of peripheral naive T cells and their relationship with thymic function in young and elderly humans. Our results show that lower naive T cell numbers were associated with a lower thymic function and higher activation and proliferating naive T cell levels. We then analyzed sjTREC numbers and relative telomere length from sorted naive T cells. Our results show that the aberrant activation and proliferation status was related to lower sjTREC numbers (a peripheral proliferation marker) and both, higher CD57 expression levels and shortened telomeres (replicative senescence-related markers). Elderly individuals show a greater contraction of the CD8 naive T cell numbers and all homeostatic alterations were more severe in this compartment. In addition, we found that low functional thymus show a CD4-biased thymocyte production. Taken together, our results suggest a homeostatic deregulation, affecting mostly the naive CD8 T cell subset, leading to the accumulation of age-associated defects in, otherwise, phenotypically naive T cells.

Indexed as

Immunologic MemoryAdultAgedAgingCD4 Lymphocyte CountCD8-Positive T-LymphocytesFemaleGene Rearrangement, T-LymphocyteHomeostasisHumansImmunoglobulin GInterleukin-7Lymphocyte SubsetsMaleMiddle AgedTelomereImmunoglobulin GInterleukin-7

Identifiers

PMID20700658
PMCPMC3127472
OpenAlexW2036956793

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.