Evidence map›Paper›PMID 35178048›Full record

ArticleFrontiers in immunology2022

Keratin 17 Promotes T Cell Response in Allergic Contact Dermatitis by Upregulating C-C Motif Chemokine Ligand 20.

Yixin Luo, Zhenlai Zhu, Bing Li, Xiaocui Bai, Hui Fang, Pei Qiao, Jiaoling Chen, Chen Zhang, Dalong Zhi, Erle Dang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  8. 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

11 authors at 2 institutions in 1 country.

Yixin LuoDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Zhenlai ZhuDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Bing LiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xiaocui BaiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Hui FangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Pei QiaoDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jiaoling ChenDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Chen ZhangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Dalong ZhiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Erle DangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Gang WangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergic contact dermatitis (ACD) is a delayed-type hypersensitivity response to skin contact allergens in which keratinocytes are critical in the initiation of early responses. Keratin 17 (K17) is a cytoskeletal protein inducible under stressful conditions and regulates multiple cellular processes, especially in skin inflammatory diseases; however, knowledge regarding its contribution to ACD pathogenesis remains ill defined. In the present study, we clarified the proinflammatory role of K17 in an oxazolone (OXA)-induced contact hypersensitivity (CHS) murine model and identified the underlying molecular mechanisms. Our results showed that K17 was highly expressed in the lesional skin of ACD patients and OXA-induced CHS mice. Mice lacking K17 exhibited alleviated OXA-induced skin inflammation, including milder ear swelling, a reduced frequency of T cell infiltration, and decreased inflammatory cytokine levels.

Indexed as

AnimalsBiomarkersChemokines, CCCytokinesDermatitis, Allergic ContactDisease SusceptibilityHumansInflammation MediatorsKeratin-17MiceT-LymphocytesBiomarkersChemokines, CCCytokinesInflammation MediatorsKeratin-17allergic contact dermatitisCCL20contact hypersensitivitykeratin 17keratinocytesT cell infiltration

Identifiers

PMID35178048
PMCPMC8845002
OpenAlexW4210364636

What Socratic 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 Socratic graph.