Evidence map›Paper›PMID 30250206›Full record

ArticleScientific reports2018

Dendritic cell maturation in the corneal epithelium with onset of type 2 diabetes is associated with tumor necrosis factor receptor superfamily member 9.

Neil S Lagali, Reza A Badian, Xu Liu, Tobias R Feldreich, Johan Ärnlöv, Tor Paaske Utheim, Lars B Dahlin, Olov Rolandsson

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 87 citations in OpenAlex.

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  15. Observational
  16. The impact of donor diabetes on corneal transplant immunity.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Article
  17. Article
  18. Redefining the human corneal immune compartment using dynamic intravital imaging.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Review
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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

8 authors at 5 institutions in 2 countries.

Neil S LagaliDepartment of Ophthalmology, Institute for Clinical and Experimental Medicine, Linköping University, 58183, Linköping, Sweden. neil.lagali@liu.se.ORCID http://orcid.org/0000-0003-1079-4361
Reza A BadianNational Centre for Optics, Vision and Eye Care, Faculty of Visual and Health Sciences, The University of South-Eastern Norway, Kongsberg, Norway.
Xu LiuØyelegesenteret i Tromsø, Fjærevegen 6, 9024, Tomasjord, Norway.
Tobias R FeldreichDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Johan ÄrnlövSchool of Health and Social Sciences, Dalarna University, Falun, Sweden.
Tor Paaske UtheimDepartment of Ophthalmology, Sørlandet Hospital Arendal, Arendal, Norway.
Lars B DahlinDepartment of Translational Medicine - Hand Surgery, Lund University, Skåne University Hospital, 20502, Malmö, Sweden.
Olov RolandssonDepartment of Public Health and Clinical Medicine, Family Medicine, Umeå University, 90187, Umeå, Sweden.
Dalarna University · SEOslo University Hospital · NOLinköping University · SELund University · SEUmeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes mellitus is characterized by a low-grade inflammation; however, mechanisms leading to this inflammation in specific tissues are not well understood. The eye can be affected by diabetes; thus, we hypothesized that inflammatory changes in the eye may parallel the inflammation that develops with diabetes. Here, we developed a non-invasive means to monitor the status of inflammatory dendritic cell (DC) subsets in the corneal epithelium as a potential biomarker for the onset of inflammation in type 2 diabetes. In an age-matched cohort of 81 individuals with normal and impaired glucose tolerance and type 2 diabetes, DCs were quantified from wide-area maps of the corneal epithelial sub-basal plexus, obtained using clinical in vivo confocal microscopy (IVCM). With the onset of diabetes, the proportion of mature, antigen-presenting DCs increased and became organized in clusters. Out of 92 plasma proteins analysed in the cohort, tumor necrosis factor receptor super family member 9 (TNFRSF9) was associated with the observed maturation of DCs from an immature to mature antigen-presenting phenotype. A low-grade ocular surface inflammation observed in this study, where resident immature dendritic cells are transformed into mature antigen-presenting cells in the corneal epithelium, is a process putatively associated with TNFRSF9 signalling and may occur early in the development of type 2 diabetes. IVCM enables this process to be monitored non-invasively in the eye.

Indexed as

AgedAntigen-Presenting CellsCell DifferentiationDendritic CellsDiabetes Mellitus, Type 2Epithelium, CornealFemaleGlucose IntoleranceHumansMaleMicroscopy, ConfocalMiddle AgedTumor Necrosis Factor Receptor Superfamily, Member 9TNFRSF9 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID30250206
PMCPMC6155153
OpenAlexW2891454336

What OpenQuestion holds

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LicenceCC BY
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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.