Evidence map›Paper›PMID 24440389›Full record

ReviewExperimental gerontology2014

Mechanisms shaping the naïve T cell repertoire in the elderly - thymic involution or peripheral homeostatic proliferation?

Qian Qi, David W Zhang, Cornelia M Weyand, Jörg J Goronzy

Open access · greenAbstract readReview
In one paragraph

Review in Experimental gerontology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Immune aging and infectious diseases.Chinese medical journal · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Immunosenescence: molecular mechanisms and diseases.Signal transduction and targeted therapy · 2023
    Review
  14. Immunology of Aging: the Birth of Inflammaging.Clinical reviews in allergy & immunology · 2023
    Review
  15. Review
  16. Review
  17. Peripheral differentiation patterns of human T cells.European journal of immunology · 2022
    Article
  18. Early age-related atrophy of cutaneous lymph nodes precipitates an early functional decline in skin immunity in mice with aging.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. T cell immune awakening in response to immunotherapy is age-dependent.European journal of cancer (Oxford, England : 1990) · 2022
    Article
  20. Review
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.

Qian QiDepartment of Medicine, Palo Alto Veterans Administration Health Care System, Palo Alto, CA 94304, United States; Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
David W ZhangDepartment of Medicine, Palo Alto Veterans Administration Health Care System, Palo Alto, CA 94304, United States; Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
Cornelia M WeyandDepartment of Medicine, Palo Alto Veterans Administration Health Care System, Palo Alto, CA 94304, United States; Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
Jörg J GoronzyDepartment of Medicine, Palo Alto Veterans Administration Health Care System, Palo Alto, CA 94304, United States; Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States. Electronic address: jgoronzy@stanford.edu.
VA Palo Alto Health Care System · US

Funding

VACCINE INDUCED IMMUNITY IN THE YOUNG AND AGEDU19AI057266 · NIAID · EMORY UNIVERSITY · PI Rafi Ahmed · 2003 to 2026
$81.7M
Vascular specific ACE expression and atherosclerosisP01HL058000 · NHLBI · VANDERBILT UNIVERSITY · PI DIKALOV, SERGEY · 1998 to 2013
$20.7M
Vaccination and infection: indicators of immunological health and responsivenessU19AI090019 · NIAID · STANFORD UNIVERSITY · PI DAVIS, MARK MORRIS · 2010 to 2015
$17.3M
Training Program in Adult and Pediatric RheumatologyT32AR050942 · NIAMS · STANFORD UNIVERSITY · PI LEWIS, DAVID BRAM, ROBINSON, WILLIAM H · 2005 to 2025
$6.6M
Oligoclonal T Cell Expansion &Rheumatoid ArthritisR01AR042527 · NIAMS · STANFORD UNIVERSITY · PI WEYAND, CORNELIA M. · 1993 to 2022
$4.8M
microRNA Regulation of T Cell SenescenceR01AI108891 · NIAID · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI GORONZY, JORG J · 2014 to 2023
$4.6M
Telomere Damage Responses and Immune AgingR01AI108906 · NIAID · STANFORD UNIVERSITY · PI WEYAND, CORNELIA M. · 2014 to 2024
$4.0M
Influence of Age on CD4 T Memory CellsR01AG045779 · NIA · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI GORONZY, JORG J · 2013 to 2023
$4.0M
CD8 T CELLS IN RHEUMATOID SYNOVITISR01AI044142 · NIAID · STANFORD UNIVERSITY · PI WEYAND, CORNELIA M. · 1999 to 2010
$2.9M
T CELLS AND AGINGR01AG015043 · NIA · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI GORONZY, JORG J · 1998 to 2008
$2.1M
CD8 T cells in Rheumatoid ArthritisR56AI044142 · NIAID · STANFORD UNIVERSITY · PI WEYAND, CORNELIA M. · 2013 to 2013
$369k
NHLBI NIH HHS P01 HL058000NIAID NIH HHS AI090019NIAID NIH HHS R01 AI044142NIAID NIH HHS R01 AI108891NIAID NIH HHS R01 AI108906NIAID NIH HHS R56 AI044142NIAID NIH HHS U19 AI057266NIAID NIH HHS U19 AI090019NIAMS NIH HHS R01 AR042527NIAMS NIH HHS T32 AR050942NIA NIH HHS R01 AG015043NIA NIH HHS R01 AG045779
6 · The paper itself

Abstract

The ability of the human immune system to repel infections is drastically diminished with age. Elderly individuals are more susceptible to new threats and are less able to control endogenous infections. The thymus, which is the sole source of new T cells, has been proposed as a target for regenerative efforts to improve immune competence, as thymic activity is dramatically reduced after puberty. In this review, we review the role of the thymus in the maintenance of T cell homeostasis throughout life and contrast the differences in mice and humans. We propose that in humans, lack of thymic T cell generation does not explain a decline in T cell receptor diversity nor would thymic rejuvenation restore diversity. Initial studies using next generation sequencing are beginning to establish lower boundaries of T cell receptor diversity. With increasing sequencing depth and the development of new statistical models, we are now in the position to test this model and to assess the impact of age on T cell diversity and clonality.

Indexed as

AdultAgedAnimalsCell ProliferationHomeostasisHumansMiceMiddle AgedReceptors, Antigen, T-CellThymus GlandT-LymphocytesT-Lymphocyte SubsetsReceptors, Antigen, T-CellAgingImmunosenescenceT cell receptor repertoireT cellsThymus

Identifiers

PMID24440389
PMCPMC4096164
OpenAlexW2086981630

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.