Evidence map›Paper›PMID 30467622›Full record

ArticleInflammation2019

The Expression of CXCL10/CXCR3 and Effect of the Axis on the Function of T Lymphocyte Involved in Oral Lichen Planus.

Jiaxiang Fang, Chen Wang, Chen Shen, Jing Shan, Xuewei Wang, Lin Liu, Yuan Fan

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 21% 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, 19 citations in OpenAlex.

  1. GPR55 negatively regulates CD8Journal of molecular histology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Lichen Planus.Frontiers in medicine · 2021
    Review
  9. 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

7 authors at 1 institution in 1 country.

Jiaxiang FangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, 210029, China.
Chen WangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, 210029, China.
Chen ShenDepartment of Special outpatient service, Hangzhou West Dental Hospital, Hangzhou, 310012, China.
Jing ShanJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, 210029, China.
Xuewei WangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, 210029, China.
Lin LiuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, 210029, China.
Yuan FanJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, 210029, China. fanyuan@njmu.edu.cn.
Nanjing Medical University · CN

Funding

National Natural Science Foundation of China 81470748
6 · The paper itself

Abstract

The etiology of oral lichen planus (OLP) is still not clear. The purpose of this study was to explore the role of CXC chemokine receptor 3(CXCR3) and its ligand CXC motif chemokine 10(CXCL10) in the pathogenesis of OLP. We examined the expression of CXCR3 and CXCL10 in OLP patients and healthy controls by quantitative real-time PCR, Western blotting, ELISAs, and immunohistochemistry, respectively. Moreover, we detected the effects of CXCL10/CXCR3 axis on T lymphocyte migration, proliferation and apoptosis by Transwell assays, CCK8 assays, and flow cytometry. We found that the expression of CXCR3 and CXCL10 was significantly increased in OLP patients. In addition, T lymphocyte migration rate of CXCL10 stimulation group was significantly higher than that of control and CXCR3 antagonist groups. After antagonizing CXCR3, the migration ability of T lymphocytes was significantly decreased, and regardless of whether CXCL10 was added in the upper chamber culture medium, the number of migrating cells was similar. The addition of CXCL10 stimulant could stimulate the proliferation of T lymphocytes, but there was no significant difference compared with control group. After antagonizing CXCR3, the proliferation rate of T lymphocytes was significantly reduced. However, there were no significant differences in the apoptosis rates of T lymphocytes between CXCL10 stimulation group, antagonist CXCR3 group, and control group. Due to the change of expression in CXCR3 and CXCL10, and its interaction in mediating the directional migration of peripheral blood T lymphocytes, affecting the proliferation of T lymphocytes, it suggests that CXCL10/CXCR3 axis may be related to the immune mechanism of OLP.

Indexed as

ApoptosisCase-Control StudiesCell MovementCell ProliferationChemokine CXCL10HumansLichen Planus, OralReceptors, CXCR3T-LymphocytesChemokine CXCL10CXCR3 protein, humanReceptors, CXCR3chemokineCXCL10CXCR3oral lichen planus

Identifiers

PMID30467622
OpenAlexW2901738685

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.