Evidence map›Paper›PMID 22396471›Full record

ReviewThe journals of gerontology. Series A, Biological sciences and medical sciences2012

T-cell biology in aging, with a focus on lung disease.

Naeun Lee, Min Sun Shin, Insoo Kang

Open access · bronzeAbstract readReview
In one paragraph

Review in The journals of gerontology. Series A, Biological sciences and medical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.9field-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

47 citing papers in PubMed, 90 citations in OpenAlex.

  1. Parenchymal and inflammatory responses to ozone exposure in the aging healthy and surfactant protein C mutant lung.American journal of physiology. Lung cellular and molecular physiology · 2025
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Aging gene signature of memory CD8Immunity & ageing : I & A · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Factors Associated with Age-Related Changes in Non-Smoking Urban Men and Women in China Determined by Low-Dose Computed Tomography Imaging.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
  14. Article
  15. T cell responses in patients with COVID-19.Nature reviews. Immunology · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. The Effects of AHCC®, a Standardized Extract of CulturedJournal of immunology research · 2019
    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

3 authors at 1 institution in 1 country.

Naeun LeeSection of Rheumatology, Department of Internal Medicine, Yale University School of Medicine, S525C TAC, 300 Cedar Street, New Haven, CT 06520, USA.
Min Sun Shin
Insoo Kang
Yale University · US

Funding

Aging and IL-7-mediated CD8+ T Cell survivalR01AG028069 · NIA · YALE UNIVERSITY · PI KANG, INSOO · 2007 to 2011
$1.6M
Investigating aging and membrane-associated T cell receptor signaling in human CDR21AG030834 · NIA · YALE UNIVERSITY · PI KANG, INSOO · 2007 to 2008
$268k
NIA NIH HHS AG028069NIA NIH HHS AG030834
6 · The paper itself

Abstract

T cells are essential for defending hosts against microorganisms and malignancy as well as for regulating the development of immune-mediated inflammatory diseases like autoimmunity. Alterations in T-cell immunity occur with aging, affecting the function and proportions of T-cell subsets. Probably, the most noticeable age-associated change in T-cell immunity is an alteration in the frequency of naive and memory CD4+ and CD8+ T cells. In fact, the frequency of naive CD4+ and CD8+ T cells decreases with aging, whereas the frequency of memory CD4+ and CD8+ T cells increases. Also, changes in T-cell proliferation, cytokine production, memory response, and cytotoxicity as well as in regulatory T-cell number and function have been reported with aging. Such alterations could contribute to the development of infections, malignancies, and inflammatory diseases that rise with aging. Of interest, T cells are closely involved in the development of inflammatory airway and lung diseases including asthma and chronic obstructive pulmonary disease, which are prevalent in the elderly people. In addition, T cells play a major role in defending host against influenza virus infection, a serious medical problem with high morbidity and mortality in the elderly people. Thus, it is conceivable that altered T-cell immunity may account in part for the development of such respiratory problems with aging. Here, we will review the recent advances in T-cell immunity and its alteration with aging and discuss the potential effects of such changes on the lung.

Indexed as

AgedAged, 80 and overAgingAnimalsAsthmaCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesHumansInfluenza, HumanLung DiseasesLymphocyte ActivationMicePulmonary Disease, Chronic ObstructiveRatsCytokines

Identifiers

PMID22396471
PMCPMC3297764
OpenAlexW2170397109

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.