Evidence map›Paper›PMID 41042382›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2025

Quantitative temporal analysis of pancreatic islet T lymphocyte and macrophage infiltration heralded by serum IgE in congenic BioBreeding (BB) Gimap5

Josefine Jönsson, Linda Faxius, Jeanette Tångrot, Krysten Vance, Stephanie Jerman, Doug Bowman, Marika Bogdani, Peter Ericsson, Rasmus Bennet, Anita Ramelius and 1 more

Abstract read
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 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
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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

11 authors.

Josefine Jönsson *Department of Clinical Sciences, Skåne University Hospital, Lund University CRC, 214 28, Malmö, Sweden. josefine.jonsson@med.lu.se.ORCID http://orcid.org/0000-0003-0709-2828
Linda Faxius *Department of Clinical Sciences, Skåne University Hospital, Lund University CRC, 214 28, Malmö, Sweden.
Jeanette TångrotDepartment of Molecular Biology, National Bioinformatics Infrastructure Sweden (NBIS), Umeå University, 901 87, Umeå, Sweden.
Krysten VanceIndica Labs, 8700 Education Pl NW, Bldg. b, Albuquerque, NM, 87114, USA.ORCID http://orcid.org/0000-0001-5647-1504
Stephanie JermanIndica Labs, 8700 Education Pl NW, Bldg. b, Albuquerque, NM, 87114, USA.
Doug BowmanIndica Labs, 8700 Education Pl NW, Bldg. b, Albuquerque, NM, 87114, USA.
Marika BogdaniUniversity of Washington, Seattle, WA, USA.
Peter EricssonDepartment of Clinical Sciences, Skåne University Hospital, Lund University CRC, 214 28, Malmö, Sweden.
Rasmus BennetDepartment of Clinical Sciences, Skåne University Hospital, Lund University CRC, 214 28, Malmö, Sweden.
Anita RameliusDepartment of Clinical Sciences, Skåne University Hospital, Lund University CRC, 214 28, Malmö, Sweden.ORCID http://orcid.org/0000-0003-2407-7785
Åke LernmarkDepartment of Clinical Sciences, Skåne University Hospital, Lund University CRC, 214 28, Malmö, Sweden.ORCID http://orcid.org/0000-0003-1735-0499

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE AND

designThe objective was to determine the association between serum IgE levels and the infiltration order of T lymphocytes and macrophages in pancreatic islets in relation to the loss of insulin and glucagon cells in presymptomatic congenic BB Gimap5-DP (Diabetes Prone) rats. MATERIAL: Congenic prediabetes BB Gimap5-DP and control Gimap5-DR (Diabetes Resistant) rats were followed every other day from 29 to 32 days of age until peak serum IgE (≤ 55 days of age).

methodsSerum IgE was measured using ELISA. The HALO™ platform facilitated quantitative image analysis of infiltrating T lymphocytes, macrophages, and target organ insulin and glucagon cells. Whole genome sequencing (WGS) was employed to identify candidate type 1 diabetes genes.

resultsSerum IgE levels increased with age in normoglycemic BB Gimap5-DP rats. Quantification of infiltrating cells per mm

conclusionsElevated IgE levels herald T lymphocyte and macrophage infiltration. Pancreatic islet inflammation was linked to Gimap4, Gimap5, and other potential candidate genes on rat chromosome 4.

Indexed as

Diabetes Mellitus, Type 1Immunoglobulin EIslets of LangerhansMacrophagesT-LymphocytesAnimalsAnimals, CongenicGlucagonInsulinMalePrediabetic StateRatsRats, Inbred BBGlucagonImmunoglobulin EInsulinAutoimmunityBeta cell massCD3+ lymphocytesED1+ macrophagesGimap proteinsIgEInsulitis

Identifiers

PMID41042382
PMCPMC12494634

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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.