Evidence map›Paper›PMID 27547234›Full record

ArticleImmunity & ageing : I & A2016

Changes in blood lymphocyte numbers with age in vivo and their association with the levels of cytokines/cytokine receptors.

Yun Lin, Jiewan Kim, E Jeffrey Metter, Huy Nguyen, Thai Truong, Ana Lustig, Luigi Ferrucci, Nan-Ping Weng

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

69 citing papers in PubMed, 134 citations in OpenAlex.

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  13. DNA methylation and prediction of biological age.Frontiers in molecular biosciences · 2025
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9 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Yun Lin *Laboratory of Molecular Biology & Immunology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD 21224 USA.
Jiewan Kim *Laboratory of Molecular Biology & Immunology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD 21224 USA.
E Jeffrey MetterTranslational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
Huy NguyenLaboratory of Molecular Biology & Immunology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD 21224 USA.
Thai TruongLaboratory of Molecular Biology & Immunology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD 21224 USA.
Ana LustigLaboratory of Molecular Biology & Immunology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD 21224 USA.
Luigi FerrucciTranslational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224 USA.
Nan-Ping WengLaboratory of Molecular Biology & Immunology, National Institute on Aging, 251 Bayview Blvd., Baltimore, MD 21224 USA.
National Institute on Aging · USNational Institutes of Health · US

Funding

Mechanisms Of Transcriptional Regulation in Memory lymphocyte Response and AgingZIAAG000757 · NIA · NATIONAL INSTITUTE ON AGING · PI WENG, NAN-PING PETER · 2009 to 2025
$7.9M
Role of Telomere In Human Lymphocyte Function and AgingZIAAG000756 · NIA · NATIONAL INSTITUTE ON AGING · PI WENG, NAN-PING PETER · 2009 to 2025
$5.5M
Intramural NIH HHS ZIA AG000756Intramural NIH HHS ZIA AG000757
6 · The paper itself

Abstract

backgroundAlterations in the number and composition of lymphocytes and their subsets in blood are considered a hallmark of immune system aging. However, it is unknown whether the rates of change of lymphocytes are stable or change with age, or whether the inter-individual variations of lymphocyte composition are stable over time or undergo different rates of change at different ages. Here, we report a longitudinal analysis of T- and B-cells and their subsets, and NK cells in the blood of 165 subjects aged from 24 to 90 years, with each subject assessed at baseline and an average of 5.6 years follow-up.

resultsThe rates of change of T-(CD4(+) and CD8(+)) and B-cells, and NK cells were relative stable throughout the adult life. A great degree of individual variations in numbers of lymphocytes and their subsets and in the rates of their changes with age was observed. Among them, CD4(+) T cells exhibited the highest degree of individual variation followed by NK cells, CD8(+) T cells, and B cells. Different types of lymphocytes had distinct trends in their rates of change which did not appear to be influenced by CMV infection. Finally, the rates of CD4(+), CD8(+) T cells, naive CD4(+) and naïve CD8(+) T cells were closely positively correlated.

conclusionOur findings provide evidence that the age-associated changes in circulating lymphocytes were at relative stable rates in vivo in a highly individualized manner and the levels of selected cytokines/cytokine receptors in serum might influence these age-associated changes of lymphocytes in circulation.

Indexed as

AgingB cellCD4 and CD8 T cellCMVHumanLymphocytesNK cellPeripheral blood

Identifiers

PMID27547234
PMCPMC4990976
OpenAlexW2517180753

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.