Evidence map›Paper›PMID 41040392›Full record

ArticlebioRxiv : the preprint server for biology2025

Insulin deficiency inhibits vaccine-mediated antibody and germinal center B-cell formation in mice.

Christopher J Genito, Pablo Ariel, Mark T Heise, Lance R Thurlow

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

4 authors.

Christopher J GenitoDepartment of Biomedical Sciences, Adams School of Dentistry, University of North Carolina at Chapel Hill.ORCID 0000-0002-9044-964X
Pablo ArielDepartment of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill.ORCID 0000-0002-8494-0379
Mark T HeiseREADDI AViDD Center, University of North Carolina at Chapel Hill.ORCID 0000-0001-5829-8477
Lance R ThurlowDepartment of Biomedical Sciences, Adams School of Dentistry, University of North Carolina at Chapel Hill.ORCID 0000-0003-1839-2922

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
Diabetes and Antibiotic Treatment FailureR01AI173004 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Brian Patrick Conlon, Lance R. Thurlow · 2023 to 2026
$2.8M
NCI NIH HHS P30 CA016086NIAID NIH HHS R01 AI173004
6 · The paper itself

Abstract

Individuals with diabetes are at increased risk for severe outcomes from vaccine-preventable infections and often mount weaker immune responses to vaccination. The diabetes-related factors underlying this impaired immunity remain unclear, but defining them is critical for improving vaccine strategies in this vulnerable population. Here, we isolated insulin deficiency as a contributing factor to decreased vaccine-mediated immune responses using a mouse model. Following immunization with an alum-adjuvanted protein subunit vaccine, insulin-deficient mice exhibited reduced antigen-specific IgG antibody responses, decreased B-cell and T-cell numbers, and lower germinal center B-cell counts within the vaccine-draining lymph node. Three-dimensional whole-organ light sheet microscopy combined with virtual reality-assisted analysis further revealed significantly smaller germinal center volumes in insulin-deficient mice compared with controls. These findings indicate that insulin deficiency can significantly constrain germinal center responses and impair antibody production from vaccination. Our results provide foundational evidence that diabetes-associated metabolic changes can significantly and negatively influence the quality of vaccine-induced immunity and highlight insulin deficiency as a potential physiological factor in this process. This work establishes a framework for defining the mechanisms of diabetes-related immune suppression and guiding the design of more effective vaccines tailored to the unique immunological requirements of people with diabetes.

Indexed as

3D imagingAlumDiabetesImmune SuppressionLight Sheet MicroscopyLymph NodeLymphocytesStreptozotocinT-cellsVirtual Reality

Identifiers

PMID41040392
PMCPMC12485872

What OpenQuestion holds

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LicenceCC BY
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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.