Evidence map›Paper›PMID 28486590›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2017

Activation-Induced Autophagy Is Preserved in CD4+ T-Cells in Familial Longevity.

Yotam Raz, Ignacio Guerrero-Ros, Andrea Maier, P Eline Slagboom, Gil Atzmon, Nir Barzilai, Fernando Macian

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Links Between Autophagy and Healthy Aging.Journal of molecular biology · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. The Critical Role of Autophagy and Phagocytosis in the Aging Brain.International journal of molecular sciences · 2024
    Review
  11. Immune aging and infectious diseases.Chinese medical journal · 2024
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Observational
  17. Proteostasis in T cell aging.Seminars in immunology · 2023
    Review
  18. Article
  19. Longevity, Centenarians and Modified Cellular Proteodynamics.International journal of molecular sciences · 2023
    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

7 authors at 3 institutions in 4 countries.

Yotam RazDepartment of Pathology, Albert Einstein College of Medicine, Bronx, New York.
Ignacio Guerrero-RosDepartment of Pathology, Albert Einstein College of Medicine, Bronx, New York.
Andrea MaierDepartment of Medicine and Aged Care, Royal Melbourne Hospital, University of Melbourne, Australia.
P Eline SlagboomDepartment of Molecular Epidemiology, Leiden University Medical Center, The Netherlands.
Gil AtzmonInstitute for Aging Research, Albert Einstein College of Medicine, Bronx, New York.
Nir BarzilaiInstitute for Aging Research, Albert Einstein College of Medicine, Bronx, New York.
Fernando MacianDepartment of Pathology, Albert Einstein College of Medicine, Bronx, New York.
Albert Einstein College of Medicine · USLeiden University Medical Center · NLThe Royal Melbourne Hospital · AU

Funding

Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2009 to 2024
$36.2M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
NIA NIH HHS P01 AG031782NIA NIH HHS P30 AG038072
6 · The paper itself

Abstract

As with many other tissues and organs, the immune system is also affected by age. Immunosenescence is characterized by a decreased ability of immune cells to mount a productive response upon exposure to new antigens. Several studies have reported that members of families with exceptional longevity show improved immune function, which might contribute to the increased life- and health-span observed in those families. Autophagy is a catabolic process that delivers cytoplasmic material to the lysosomes for degradation. Defective autophagy is known to be associated with age in several cell types and tissues and its dysregulation is related to age-associated diseases. In T-cells, autophagy has an essential role in modulating protein and organelle homeostasis and in the regulation of activation-induced responses. In this study, using two different cohorts of individuals belonging to families with exceptional longevity, we show that CD4+ T-cells isolated from the offspring of parents with exceptional longevity show improved activation-induced autophagic activity compared with age-matched controls. Interestingly, increased autophagy is positively correlated with increased interferon-γ production. In conclusion, autophagy appears to be better maintained in members of families with extended longevity and positively correlates with improved T-cell function.

Indexed as

AgedAged, 80 and overAutophagyCase-Control StudiesCD4-Positive T-LymphocytesEnzyme-Linked Immunosorbent AssayFemaleFluorescent Antibody TechniqueHomeostasisHumansLongevityLymphocyte ActivationMalePhenotypeCD4+ T-cellCentenariansImmunosenescenceMacroautophagyProteostasis

Identifiers

PMID28486590
PMCPMC5861944
OpenAlexW2613309479

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.