Evidence map›Paper›PMID 26155150›Full record

ArticleCentral-European journal of immunology2014

Expression of interleukin-17 in lesions of erythema multiforme may indicate a role for T helper 17 cells.

Zeynep Meltem Akkurt, Derya Uçmak, Gül Türkcü, Hatice Yüksel, Kenan Yildiz, Mustafa Arıca

Open access · goldAbstract read
In one paragraph

Article in Central-European journal of immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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

6 authors at 2 institutions in 1 country.

Zeynep Meltem AkkurtDepartment of Dermatology, Dicle University Faculty of Medicine, Diyarbakir, Turkey.
Derya UçmakDepartment of Dermatology, Dicle University Faculty of Medicine, Diyarbakir, Turkey.
Gül TürkcüDepartment of Pathology, Dicle University Faculty of Medicine, Diyarbakir, Turkey.
Hatice YükselDepartment of Biochemistry, Dicle University Faculty of Medicine, Diyarbakir, Turkey.
Kenan YildizDiyarbakir Training and Research Hospital, Diyarbakir, Turkey.
Mustafa ArıcaDepartment of Dermatology, Dicle University Faculty of Medicine, Diyarbakir, Turkey.
Dicle University · TRDiyarbakır Askeri Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe aim of this study was to evaluate levels of interleukin (IL)-2, IL-6, IL-8, IL-10, IL-17A and interferon γ (IFN-γ) in the serum of patients with erythema multiforme (EM) and to search for the presence of IL-17-expressing cells in lesional samples of EM. MATERIAL AND

methodsA total of 32 patients (22 females and 10 males) diagnosed with EM of the minor or major type were included in the study. Levels of IL-2, IL-6, IL-8, IL-10, IL-17A and IFN-γ in the serum were determined and compared with healthy controls. Biopsy specimens were stained with haematoxylin and eosin (HE) and monoclonal antibodies to CD4, CD8 and IL-17 for immunohistochemical examination.

resultsIL-2, 6, 8 and 17A were significantly higher in the patient group (p = 0.016, p = 0.001, p = 0.004, p = 0.006, respectively) and levels of IL-10 were significantly lower than in the control group (p = 0.046). The cellular infiltrate in lesions of EM was composed mainly of CD4+ T lymphocytes. The presence of IL-17-expressing cells, at proportion of 5 to 50%, was observed in the infiltrate.

conclusionsThe demonstration of IL-17-expressing cells in lesions of EM in this study has brought forth the assumption that Th17 cells may be involved in the pathogenesis of EM.

Indexed as

erythema multiformeinterleukin-17T helper 1T helper 17

Identifiers

PMID26155150
PMCPMC4439997
OpenAlexW2184968298

What OpenQuestion holds

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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.