Evidence map›Paper›PMID 38700313›Full record

ArticleBalkan medical journal2024

Thymic Stromal Lymphopoietin Activates Mouse Dendritic Cells Through the JAK/SYK Pathway in Promoting Th17 Response in Psoriasis.

Cuihao Song, Jie Sun, Zhenkai Zhao, Xu Zhang, Xiangyu Ding, Xiaoqiang Liang, Jia Bai, Liyuan Xing, Lingling Gong, Chengxin Li and 1 more

Abstract read
In one paragraph

Article in Balkan medical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. A review of core immuno-inflammatory mechanisms and key regulatory targets in psoriasis.American journal of clinical and experimental immunology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
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.

Cuihao SongDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0009-3621-7483
Jie Sun305 Hospital of People's Liberation Army, Beijing, China.ORCID 0009-0001-1175-9624
Zhenkai ZhaoDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0003-9906-6658
Xu ZhangDepartment of Clinical Laboratory, The First Medical Center of PLA General Hospital, Beijing, China.ORCID 0009-0000-4244-6498
Xiangyu DingDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0004-3123-9855
Xiaoqiang LiangDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0006-1852-0858
Jia BaiDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0005-2887-1507
Liyuan XingDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0001-9266-0908
Lingling GongDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0006-0112-3426
Chengxin LiDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0000-1882-5121
Biwen LinDepartment of Dermatology, PLA General Hospital, Beijing, China.ORCID 0009-0009-8871-4553

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Psoriasis is a chronic inflammatory skin disease that has no cure. While the specific cause of psoriasis is unknown, interactions between immune cells and inflammatory cytokines are believed to be important in its pathogenesis. Thymic stromal lymphopoietin (TSLP) is a cytokine produced by epithelial cells that profoundly affects dendritic cells (DCs) and is involved in allergy and inflammatory diseases. In some studies, its expression is higher in the skin of psoriasis patients, whereas it is increased in treated psoriasis patients when compared with untreated patients in others. Aims: To investigate the role of TSLP in the pathogenesis of psoriasis. Study Design: In vitro and in vivo study. Methods: To investigate the effect of TSLP on psoriasis in vivo, a mouse psoriasis model and shRNA targeting TSLP to reduce its expression were used. Mouse primary bone marrow dendritic cells (BMDCs) were cultured in vitro and used to investigate the signaling pathways activated by TSLP. Results: We found that reducing TSLP expression in psoriasis skin alleviated disease severity. TSLP activated the Janus kinase (JAK)/SYK pathway in psoriatic skin. In vitro studies with BMDCs demonstrated that TSLP increased DC maturation through the JAK/SYK pathway and activated DCs-secreted cytokines that stimulated CD4 Conclusion: These findings indicated that TSLP exerted its immune-modulating effect in psoriasis through the JAK/SYK pathway.

Indexed as

CytokinesDendritic CellsPsoriasisTh17 CellsThymic Stromal LymphopoietinAnimalsDisease Models, AnimalHumansJanus KinasesMiceSignal TransductionSyk KinaseCytokinesJanus KinasesSyk KinaseThymic Stromal LymphopoietinTSLP protein, mouse

Identifiers

PMID38700313
PMCPMC11077931

What OpenQuestion holds

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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.