Evidence map›Paper›PMID 28616771›Full record

ArticleGeroScience2017

Androgen supplementation improves some but not all aspects of immune senescence in aged male macaques.

Maham Rais, Randall M Wilson, Henryk F Urbanski, Ilhem Messaoudi

Open access · bronzeAbstract read
In one paragraph

Article in GeroScience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Chronic Kidney Disease and Cellular Senescence.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Effects of saponins RbFrontiers in molecular biosciences · 2024
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Immune mechanisms of hypertension.Nature reviews. Immunology · 2019
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

4 authors at 2 institutions in 1 country.

Maham RaisGraduate program in Biomedical Sciences, School of Medicine, University of California, Riverside, CA, USA.
Randall M WilsonGraduate program in Cell, Molecular, and Developmental Biology, University of California, Riverside, CA, USA.
Henryk F UrbanskiDivision of Neuroscience and Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, USA.
Ilhem MessaoudiGraduate program in Biomedical Sciences, School of Medicine, University of California, Riverside, CA, USA. imessaou@uci.edu.
University of California, Riverside · USOregon Health & Science University · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Viral Testing CoreU42OD010426 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Samuel Peterson · 2013 to 2026
$6.0M
Cognition in Rhesus Macaques in Relation to Age and Endocrine StatusR01AG036670 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI URBANSKI, HENRYK F · 2011 to 2015
$3.2M
Modulation of immune senescence by androgen treatment in aged male macaquesR21AG043896 · NIA · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI MESSAOUDI, ILHEM, URBANSKI, HENRYK F · 2013 to 2014
$443k
National Institutes of Health AG036670National Institutes of Health AG043896National Institutes of Health OD-010426National Institutes of Health OD011092NIA NIH HHS R01 AG036670NIA NIH HHS R21 AG043896NIH HHS P51 OD011092NIH HHS U42 OD010426
6 · The paper itself

Abstract

Aging leads to a progressive decline in immune function commonly referred to as immune senescence, which results in increased incidence and severity of infection. In addition, older males experience a significant disruption in their levels of circulating androgens, notably testosterone and dehydroepiandrosterone (DHEA), which has been linked to sarcopenia, osteoporosis, cardiovascular disease, and diabetes. Since sex steroid levels modulate immune function, it is possible that the age-related decline in androgen levels can also affect immune senescence. Therefore, in this study, we evaluated the pleiotropic effects of physiological androgen supplementation in aged male rhesus macaques (n = 7/group) on immune cell subset frequency and response to vaccination. As expected, frequency of naïve CD4 and CD8 T cells declined in aged non-treated macaques, while that of memory T cells increased. In contrast, frequency of naïve and memory T cells remained stable in androgen-supplemented males. In addition, levels of inflammatory cytokines increased less steeply in supplemented aged males compared to the aged controls. Despite these changes, androgen-supplemented animals only showed modest improvement in antibody responses following vaccination compared to age non-treated controls. These data indicate that short-term physiological androgen supplementation can improve some but not all aspects of immune senescence.

Indexed as

AndrogensAndropauseImmune senescenceInflammationRhesus macaquesT cells

Identifiers

PMID28616771
PMCPMC5636781
OpenAlexW2733628473

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.