Evidence map›Paper›PMID 42079244›Full record

ArticlebioRxiv : the preprint server for biology2026

Ketone ester supplementation in aged mice reduces activation of B cell subsets.

Ariel Adkisson-Floro, Ritesh Tiwari, Mitsunori Nomura, Rebeccah R Riley, Ryan Kwok, Durai Sellegounder, Mir M Khalid, Herbert G Kasler, John C Newman, Eric Verdin

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Ariel Adkisson-FloroBuck Institute for Research on Aging, Novato, CA.ORCID 0009-0004-7460-8059
Ritesh TiwariBuck Institute for Research on Aging, Novato, CA.
Mitsunori NomuraBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0002-1811-4917
Rebeccah R RileyBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0002-5870-6837
Ryan KwokBuck Institute for Research on Aging, Novato, CA.
Durai SellegounderBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0002-0776-0307
Mir M KhalidBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0002-1862-6795
Herbert G KaslerBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0002-6660-4267
John C NewmanBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0002-8455-0100
Eric VerdinBuck Institute for Research on Aging, Novato, CA.ORCID 0000-0003-3703-3183

Funding

Training in Basic Research on Aging and Age-Related DiseaseT32AG000266 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI Lisa M Ellerby · 1998 to 2026
$13.8M
USC Geroscience Training in the Biology of AgingT32AG052374 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sean P CURRAN · 2016 to 2026
$5.3M
Mechanisms of the signaling metabolite β-hydroxybutyrate in Alzheimer's disease and the aging brainR01AG067333 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI John C Newman · 2020 to 2026
$4.8M
Geroscience metabolites beta-hydroxybutyrate and NAD+ linking inflammation and neuroenergetic failure in deliriumR01AG068025 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI NEWMAN, JOHN C · 2020 to 2024
$4.2M
Cellular senescence and Associated Lysosomal Dysfunction in Immune AgingU01AI180158 · NIAID · BUCK INSTITUTE FOR RESEARCH ON AGING · PI Birgit Schilling, Eric M. Verdin · 2024 to 2026
$2.1M
NIAID NIH HHS U01 AI180158NIA NIH HHS R01 AG067333NIA NIH HHS R01 AG068025NIA NIH HHS T32 AG000266NIA NIH HHS T32 AG052374
6 · The paper itself

Abstract

Aging in the immune system results in increased susceptibility to infections, exacerbated autoimmunity, and reduced responsiveness to vaccines. However, there are no current established interventions for immune aging. Ketogenic diets and fasting have been researched as interventions against other aspects of aging and age-related diseases, and they work in part by increasing circulating levels of ketone bodies, which have anti-inflammatory properties and can boost T cell function. Exogenous ketones, such as ketone esters, are currently being studied as a more accessible approach to obtain the benefits of ketone bodies through direct supplementation. Here, we investigated whether ketone ester supplementation improves immune function during aging. Aged (19-month-old) C57BL/6JN mice were given a diet supplemented with the ketone ester or a control diet for 15 weeks. We found that the ketone ester diet decreased activation of B cells, especially age-associated B cells, in the spleen. In spite of this decrease in activation, mice on the ketone ester diet showed no impairment in antibody production after nitrophenyl-ovalbumin immunization. The ketone ester diet also inhibited glucose dependence and translation of age-associated B cells, likely through inhibition of mTOR signaling via ketone bodies. Our study elucidates the effect of ketone esters on B cells in the context of aging and unveils a new immunoregulatory role of ketone bodies on B cells.

Identifiers

PMID42079244
PMCPMC13131667

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.