Evidence map›Paper›PMID 19941883›Full record

ArticleMechanisms of ageing and development2010

Maintenance of naïve CD8 T cells in nonagenarians by leptin, IGFBP3 and T3.

Jian Chen, Jun Li, Fei Chu Lim, Qi Wu, Daniel C Douek, Donald K Scott, Eric Ravussin, Hui-Chen Hsu, S Michal Jazwinski, John D Mountz and 1 more

Abstract readComparative Study
In one paragraph

Article in Mechanisms of ageing and development, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Dysregulation of T Follicular Helper Cells in Lupus.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Review
  10. Review
  11. Article
  12. Premature T Cell Senescence in Pediatric CKD.Journal of the American Society of Nephrology : JASN · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Reversing T cell immunosenescence: why, who, and how.Age (Dordrecht, Netherlands) · 2013
    Review
  18. Article
  19. Review
  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

11 authors at 5 institutions in 1 country.

Jian ChenDepartment of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Jun Li
Fei Chu Lim
Qi Wu
Daniel C Douek
Donald K Scott
Eric Ravussin
Hui-Chen Hsu
S Michal Jazwinski
John D Mountz
Louisiana Healthy Aging Study
University of Alabama at Birmingham · USBirmingham VA Medical Center · USPennington Biomedical Research Center · USTulane University · USUniversity of Pittsburgh Medical Center · US

Funding

VASCULAR STATUS, PHYSICAL FUNCTION, AND HEALTHY AGINGP01AG022064 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI JAZWINSKI, S MICHAL · 2004 to 2010
$9.6M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
InflammationZIAAI005031 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DOUEK, DANIEL CESAR · 2009 to 2024
$5.9M
NIAMS NIH HHS P30 AR048311NIA NIH HHS P01 AG022064
6 · The paper itself

Abstract

Research into the age-associated decline in the immune system has focused on the factors that contribute to the accumulation of senescent CD8 T cells. Less attention has been paid to the non-immune factors that may maintain the pool of naïve CD8 T cells. Here, we analyzed the status of the naïve CD8 T-cell population in healthy nonagenarians (>or=90-year-old), old (60-79-year-old), and young (20-34-year-old) subjects. Naïve CD8 T cells were defined as CD28(+)CD95(-) as this phenotype showed a strong co-expression of the CD45RA(+), CD45RO(-), and CD127(+) phenotypes. Although there was an age-associated decline in the percentage of CD28(+)CD95(-) CD8 T cells, the healthy nonagenarians maintained a pool of naïve CD28(+)CD95(-) cells that contained T-cell receptor excision circles (TREC)(+) cells. The percentages of naïve CD28(+)CD95(-) CD8 T cells in the nonagenarians correlated with the sera levels of insulin-like growth factor binding protein 3 (IGFBP3) and leptin. Higher levels of triiodothyronine (T3) negatively correlated with the accumulation of TREC(-)CD28(-)CD95(+) CD8 T cells from nonagenarians. These results suggest a model in which IGFBP3, leptin and T3 act as non-immune factors to maintain a larger pool of naïve CD8 T cells in healthy nonagenarians.

Indexed as

AdultAgedAged, 80 and overAge FactorsAgingCD28 AntigensCD8-Positive T-LymphocytesCellular SenescenceCohort Studiesfas ReceptorHumansImmunologic MemoryImmunophenotypingInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor Binding ProteinsInterleukin-7 Receptor alpha SubunitCD28 Antigensfas ReceptorIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor Binding ProteinsInterleukin-7 Receptor alpha SubunitLeptinLeukocyte Common AntigensPTPRC protein, humanTriiodothyronine

Identifiers

PMID19941883
PMCPMC2843505
OpenAlexW2080924958

What OpenQuestion holds

Textmetadata
LicenceTDM
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.