Evidence map›Paper›PMID 40912723›Full record

ArticleBMJ open diabetes research & care2025

TLR5 influences the development of type 1 diabetes.

Karsten Buschard, Lars Krogvold, Flemming Pociot, Ivan Gerling, Rikke Thea, Knut Dahl-Jørgensen, Camilla Hartmann Friis Hansen

Abstract read
In one paragraph

Article in BMJ open diabetes research & care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Karsten BuschardThe Bartholin Institute, Department of Pathology, Rigshospitalet, Copenhagen, Denmark buschard@dadlnet.dk.ORCID http://orcid.org/0000-0002-0126-7423
Lars KrogvoldDepartment of Pediatrics and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Flemming PociotT1D Biology, Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Ivan GerlingMedicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Rikke TheaVeterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg Campus, Frederiksberg, Denmark.ORCID http://orcid.org/0009-0000-3862-3922
Knut Dahl-JørgensenDepartment of Pediatrics and Adolescent Medicine, Oslo University Hospital, Oslo, Norway.
Camilla Hartmann Friis HansenVeterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg Campus, Frederiksberg, Denmark.ORCID http://orcid.org/0000-0002-1860-385X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In mammalian and human life, it is important that the immune system defends against microorganisms. Although there is a huge overlap, innate cells are good against bacteria, whereas T cells are good against viruses, mainly because of antibody production via T helper and B lymphocytes. Toll-like receptor 5 (TLR5) is a regulator; when it is highly expressed, T cells are inhibited, and innate cells are favored. In glucose-activated pancreatic islets, RESEARCH DESIGN AND

methodsWe investigated mRNA from the islets of Langerhans in patients with newly diagnosed T1D for

resultsIslet mRNA for

conclusionsIn the present study, we find a low expression of mRNA for

Indexed as

Diabetes Mellitus, Type 1Islets of LangerhansToll-Like Receptor 5AdolescentAdultAnimalsCase-Control StudiesFemaleHumansMaleMiceMice, Inbred NODRNA, MessengerT-LymphocytesYoung AdultRNA, MessengerTLR5 protein, humanToll-Like Receptor 5Autoimmune DiseasesDiabetes Mellitus, Type 1T-Lymphocytes

Identifiers

PMID40912723
PMCPMC12414181

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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.