Evidence map›Paper›PMID 30661459›Full record

ArticleCell cycle (Georgetown, Tex.)2019

IL-17 produced by Th17 cells alleviates the severity of fungal keratitis by suppressing CX43 expression in corneal peripheral vascular endothelial cells.

Xiu-Hong Qin, Xiang Ma, Shi-Feng Fang, Zhen-Zhen Zhang, Jian-Min Lu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Frontiers in cellular and infection microbiology · 2025
    Article
  4. Review
  5. Alteration of mJournal of clinical medicine · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Update on the management of fungal keratitis.International ophthalmology · 2021
    Review
  12. Review
  13. Article
  14. Review
  15. How doesWorld journal of gastroenterology · 2019
    Review
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

5 authors at 2 institutions in 1 country.

Xiu-Hong Qina Department of Ophthalmology , The First Affiliated Hospital of Dalian Medical University , Dalian , P. R. China.
Xiang Maa Department of Ophthalmology , The First Affiliated Hospital of Dalian Medical University , Dalian , P. R. China.
Shi-Feng Fanga Department of Ophthalmology , The First Affiliated Hospital of Dalian Medical University , Dalian , P. R. China.
Zhen-Zhen Zhangb Department of Ophthalmology , Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine , Shanghai , P. R. China.
Jian-Min Lua Department of Ophthalmology , The First Affiliated Hospital of Dalian Medical University , Dalian , P. R. China.
Dalian Medical University · CNShanghai Ninth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fungal keratitis is a relatively common ocular disease requiring positive medical management combined with surgical intervention. Interleukin-17 (IL-17) was reported to promote the activation and mobilization of neutrophile granulocyte to foci of inflammation. This study investigated the effect of IL-17 production from Th17 cells on the progression of fungal keratitis. A mouse model of fungal keratitis induced by Candida albicans was successfully constructed to detect infiltration of inflammatory cells in corneal tissues by hematoxylin-eosin (HE) staining and immunohistochemistry. Fungal load capacity of mouse cornea was also detected. The regulatory role of IL-17 in fungal keratitis with the involvement of CX43 was investigated with the relevant expression of inflammatory factors detected and activation of vascular endothelial cells assessed. Furthermore, in vivo experiment was also performed to confirm the role of CX43 in keratitis. Mice with fungal keratitis showed increased level of inflammatory cytokines and infiltration of inflammatory cells. Silencing IL-17 in Th17 cells and overexpressing CX43 could inhibit the activation of vascular endothelial cells. Besides, CX43 knockdown in vivo alleviated fungal keratitis in mice. The possible mechanism of the above findings could be IL-17 inhibiting the level of CX43 through the AKT signaling pathway. Taken together, IL-17 could inhibit the occurrence and development of fungal keratitis by suppressing CX43 expression through the AKT signaling pathway. Therefore, this study provides a potential target for the treatment of fungal keratitis.

Indexed as

AnimalsCandida albicansCandidiasisCells, CulturedConnexin 43CorneaCytokinesDisease Models, AnimalEndothelial CellsEndothelium, VascularEye Infections, FungalFemaleInterleukin-17KeratitisMiceMice, Inbred BALB CConnexin 43CytokinesGJA1 protein, mouseInterleukin-17Proto-Oncogene Proteins c-aktconnexin43Fungal keratitisinterleukin-17vascular endothelial cell

Identifiers

PMID30661459
PMCPMC6380429
OpenAlexW2908605970

What OpenQuestion holds

Textmetadata
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.