Evidence map›Paper›PMID 32514279›Full record

ArticleImmunity & ageing : I & A2020

The impact of body mass index on adaptive immune cells in the human bone marrow.

Luca Pangrazzi, Erin Naismith, Carina Miggitsch, Jose' Antonio Carmona Arana, Michael Keller, Beatrix Grubeck-Loebenstein, Birgit Weinberger

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Copper dysregulation in cardiometabolic disease: copper deficiency versus cuproptosis.Apoptosis : an international journal on programmed cell death · 2026
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  8. CD4Neurobiology of stress · 2024
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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 1 institution in 1 country.

Luca PangrazziDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Erin NaismithDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Carina MiggitschDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Jose' Antonio Carmona AranaDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Michael KellerDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Beatrix Grubeck-LoebensteinDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Birgit WeinbergerDepartment of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, Rennweg, 10 Innsbruck, Austria.
Universität Innsbruck · AT

Funding

Austrian Science Fund FWF W 1253
6 · The paper itself

Abstract

backgroundObesity has been associated with chronic inflammation and oxidative stress. Both conditions play a determinant role in the pathogenesis of age-related diseases, such as immunosenescence. Adipose tissue can modulate the function of the immune system with the secretion of molecules influencing the phenotype of immune cells. The importance of the bone marrow (BM) in the maintenance of antigen-experienced adaptive immune cells has been documented in mice. Recently, some groups have investigated the survival of effector/memory T cells in the human BM. Despite this, whether high body mass index (BMI) may affect immune cells in the BM and the production of molecules supporting the maintenance of these cells it is unknown.

methodsUsing flow cytometry, the frequency and the phenotype of immune cell populations were measured in paired BM and PB samples obtained from persons with different BMI. Furthermore, the expression of BM cytokines was assessed. The influence of cytomegalovirus (CMV) on T cell subsets was additionally considered, dividing the donors into the CMV

resultsOur study suggests that increased BMI may affect both the maintenance and the phenotype of adaptive immune cells in the BM. While the BM levels of IL-15 and IL-6, supporting the survival of highly differentiated T cells, and oxygen radicals increased in overweight persons, the production of IFNγ and TNF by CD8

conclusionOur work suggests that, in addition to aging and CMV, obesity may represent an additional risk factor for immunosenescence in adaptive immune cells. Metabolic interventions may help in improving the fitness of the immune system in the elderly.

Indexed as

BMIBone marrowCMVHumanPeripheral bloodT cells

Identifiers

PMID32514279
PMCPMC7251898
OpenAlexW3028944412

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.