Evidence map›Paper›PMID 24608112›Full record

ArticlePloS one2014

Reactive oxygen species prevent imiquimod-induced psoriatic dermatitis through enhancing regulatory T cell function.

Hyung-Ran Kim, Anbok Lee, Eun-Jeong Choi, Min-Pyo Hong, Jeong-Hae Kie, Woosung Lim, Hyeon Kook Lee, Byung-In Moon, Ju-Young Seoh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

54 citing papers in PubMed, 98 citations in OpenAlex.

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  11. Macrophage Functions in Psoriasis: Lessons from Mouse Models.International journal of molecular sciences · 2024
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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

9 authors at 3 institutions in 2 countries.

Hyung-Ran KimDepartment of Microbiology, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Anbok LeeDepartment of Surgery, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Eun-Jeong ChoiDepartment of Microbiology, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Min-Pyo HongCollege of Arts and Sciences, Boston College, Chestnut Hill, Massachusetts, United States of America.
Jeong-Hae KiePathology, National Health Insurance Cooperation Ilsan Hospital, Koyang, Korea.
Woosung LimDepartment of Surgery, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Hyeon Kook LeeDepartment of Surgery, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Byung-In MoonDepartment of Surgery, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Ju-Young SeohDepartment of Microbiology, Ewha Womans University Graduate School of Medicine, Seoul, Korea.
Ewha Womans University · KRBoston College · USNational Health Insurance Service · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a chronic inflammatory skin disease resulting from immune dysregulation. Regulatory T cells (Tregs) are important in the prevention of psoriasis. Traditionally, reactive oxygen species (ROS) are known to be implicated in the progression of inflammatory diseases, including psoriasis, but many recent studies suggested the protective role of ROS in immune-mediated diseases. In particular, severe cases of psoriasis vulgaris have been reported to be successfully treated by hyperbaric oxygen therapy (HBOT), which raises tissue level of ROS. Also it was reported that Treg function was closely associated with ROS level. However, it has been only investigated in lowered levels of ROS so far. Thus, in this study, to clarify the relationship between ROS level and Treg function, as well as their role in the pathogenesis of psoriasis, we investigated imiquimod-induced psoriatic dermatitis (PD) in association with Treg function both in elevated and lowered levels of ROS by using knockout mice, such as glutathione peroxidase-1(-/-) and neutrophil cytosolic factor-1(-/-) mice, as well as by using HBOT or chemicals, such as 2,3-dimethoxy-1,4-naphthoquinone and N-acetylcysteine. The results consistently showed Tregs were hyperfunctional in elevated levels of ROS, whereas hypofunctional in lowered levels of ROS. In addition, imiquimod-induced PD was attenuated in elevated levels of ROS, whereas aggravated in lowered levels of ROS. For the molecular mechanism that may link ROS level and Treg function, we investigated the expression of an immunoregulatory enzyme, indoleamine 2,3-dioxygenase (IDO) which is induced by ROS, in PD lesions. Taken together, it was implied that appropriately elevated levels of ROS might prevent psoriasis through enhancing IDO expression and Treg function.

Indexed as

AcetylcysteineAminoquinolinesAnimalsDermatitisDisease ProgressionGlutathione PeroxidaseGlutathione Peroxidase GPX1Hyperbaric OxygenationImiquimodIndoleamine-Pyrrole 2,3,-DioxygenaseMice, Inbred C57BLNADPH OxidasesNaphthoquinonesPsoriasisReactive Oxygen SpeciesT-Lymphocytes, Regulatory2,3-dimethoxy-1,4-naphthoquinoneAcetylcysteineAminoquinolinesGlutathione PeroxidaseGlutathione Peroxidase GPX1Gpx1 protein, mouseImiquimodIndoleamine-Pyrrole 2,3,-DioxygenaseNADPH OxidasesNaphthoquinonesneutrophil cytosolic factor 1Reactive Oxygen Species

Identifiers

PMID24608112
PMCPMC3946742
OpenAlexW2077121920

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.