Evidence map›Paper›PMID 32694825›Full record

ArticleNature metabolism2020

Eosinophils regulate adipose tissue inflammation and sustain physical and immunological fitness in old age.

Daniel Brigger, Carsten Riether, Robin van Brummelen, Kira I Mosher, Alicia Shiu, Zhaoqing Ding, Noemi Zbären, Pascal Gasser, Pascal Guntern, Hanadie Yousef and 16 more

Open access · greenAbstract read
In one paragraph

Article in Nature metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

72 citing papers in PubMed, 104 citations in OpenAlex.

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  17. Article
  18. Immunosenescence: signaling pathways, diseases and therapeutic targets.Signal transduction and targeted therapy · 2025
    Review
  19. Aging and immunity: the age-old tango.Genes & development · 2025
    Review
  20. Article

12 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

26 authors at 11 institutions in 3 countries.

Daniel BriggerDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.
Carsten RietherTumor Immunology, Department for BioMedical Reserach, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0001-7512-513X
Robin van BrummelenDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0003-1182-8519
Kira I MosherDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-3041-3186
Alicia ShiuDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Zhaoqing DingDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Noemi ZbärenDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0003-2968-0938
Pascal GasserDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0003-3708-1660
Pascal GunternDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0001-8840-8577
Hanadie YousefDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Joseph M CastellanoNash Family Department of Neuroscience, Department of Neurology, Friedman Brain Institute, Ronald M. Loeb Center for Alzheimer's Disease, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-8026-6292
Federico StorniDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.
Neill Graff-RadfordDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Markus BritschgiDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-6151-4257
Denis GrandgirardInstitute for Infectious Diseases, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0002-4151-5196
Magdalena HinterbrandnerTumor Immunology, Department for BioMedical Reserach, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0003-1682-3573
Mark SiegristDepartment for BioMedical Research, University of Bern, Bern, Switzerland.
Norman MoullanLaboratory of Integrative and Systems Physiology, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Willy HofstetterDepartment for BioMedical Research, University of Bern, Bern, Switzerland.
Stephen L LeibInstitute for Infectious Diseases, University of Bern, Bern, Switzerland.ORCID http://orcid.org/0000-0002-1106-6123
Peter M VilligerDepartment of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland.
Johan AuwerxLaboratory of Integrative and Systems Physiology, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.ORCID http://orcid.org/0000-0002-5065-5393
Saul A VilledaDepartment of Anatomy, University of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-2726-9582
Tony Wyss-CorayDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-5893-0831
Mario Noti *Institute of Pathology, Division of Experimental Pathology, University of Bern, Bern, Switzerland. mario.noti@rd.nestle.com.ORCID http://orcid.org/0000-0001-9386-1245
Alexander Eggel *Department of Rheumatology, Immunology and Allergology, Bern University Hospital, University of Bern, Bern, Switzerland. alexander.eggel@dbmr.unibe.ch.ORCID http://orcid.org/0000-0001-8746-3339
University of Bern · CHÉcole Polytechnique Fédérale de Lausanne · CHAllen Institute for Brain Science · USAmplitude Technologies (France) · FRJohnson & Johnson (United States) · USMayo Clinic in Florida · USNeurosciences Institute · USRoche (Switzerland) · CHStanford University · USUniversity of California, Berkeley · USUniversity of California, San Francisco · US

Funding

A Bioorthogonal Approach to Study Mammalian AgingDP1AG053015 · NIA · STANFORD UNIVERSITY · PI WYSS-CORAY, TONY · 2015 to 2019
$3.7M
Translational Systems Genetics of Mitochondria, Metabolism, and AgingR01AG043930 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WILLIAMS, ROBERT W. · 2013 to 2017
$2.5M
Mechanisms of brain rejuvenationR01AG053382 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VILLEDA, SAUL A · 2016 to 2020
$2.0M
Circulatory Rejuvenating Factors for the BrainR01AG045034 · NIA · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI WYSS-CORAY, TONY · 2013 to 2017
$1.4M
NIA NIH HHS DP1 AG053015NIA NIH HHS R01 AG043930NIA NIH HHS R01 AG045034NIA NIH HHS R01 AG053382
6 · The paper itself

Abstract

Adipose tissue eosinophils (ATEs) are important in the control of obesity-associated inflammation and metabolic disease. However, the way in which ageing impacts the regulatory role of ATEs remains unknown. Here, we show that ATEs undergo major age-related changes in distribution and function associated with impaired adipose tissue homeostasis and systemic low-grade inflammation in both humans and mice. We find that exposure to a young systemic environment partially restores ATE distribution in aged parabionts and reduces adipose tissue inflammation. Approaches to restore ATE distribution using adoptive transfer of eosinophils from young mice into aged recipients proved sufficient to dampen age-related local and systemic low-grade inflammation. Importantly, restoration of a youthful systemic milieu by means of eosinophil transfers resulted in systemic rejuvenation of the aged host, manifesting in improved physical and immune fitness that was partially mediated by eosinophil-derived IL-4. Together, these findings support a critical function of adipose tissue as a source of pro-ageing factors and uncover a new role of eosinophils in promoting healthy ageing by sustaining adipose tissue homeostasis.

Indexed as

ImmunityAdipose TissueAdipose Tissue, WhiteAdultAgedAgingAnimalsEosinophilsGene Expression RegulationGlucose Tolerance TestHomeostasisHumansInflammationInterleukin-4MiceMice, Inbred C57BLIL4 protein, humanInterleukin-4

Identifiers

PMID32694825
PMCPMC7438316
OpenAlexW3040521372

What OpenQuestion holds

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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.