Evidence map›Paper›PMID 35950112›Full record

ArticlePostepy dermatologii i alergologii2022

Regulation of eotaxin expression in skin allergic diseases.

Cheng Peng, Hualin Zhang, Jishun Yang, Jianguo Xu, Shikui Guan, Jianjun Xia, Quangang Zhu, Benming You, Yu Zhu, Jinhong Hu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Postepy dermatologii i alergologii, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. A Comprehensive Review of Kimura Disease.Head and neck pathology · 2025
    Pooled it
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 5 institutions in 2 countries.

Cheng PengDepartment of Health Management, Beidaihe Rest and Recuperation Center, Joint Logistic Support Force of the Chinese People's Liberation Army, Qinhuangdao, Hebei, China.
Hualin ZhangDepartment of Pharmacy, 81 Group Army Hospital, PLA, Zhangjiakou, Hebei, China.
Jishun YangMedical Security Center, PLA Naval Medical Center, Shanghai, China.
Jianguo XuDepartment of Plastic Surgery, the First Affiliated Hospital of PLA Naval Military Medical University, Shanghai, China.
Shikui GuanDepartment of Health Management, Beidaihe Rest and Recuperation Center, Joint Logistic Support Force of the Chinese People's Liberation Army, Qinhuangdao, Hebei, China.
Jianjun XiaDepartment of Health Management, Beidaihe Rest and Recuperation Center, Joint Logistic Support Force of the Chinese People's Liberation Army, Qinhuangdao, Hebei, China.
Quangang ZhuDepartment of Pharmacy, Shanghai Dermatology Hospital, Shanghai, China.
Benming YouDepartment of Pharmacy, Changhai Hospital, Navy Medical University, Shanghai, China.
Yu ZhuDepartment of Pharmacy, Changhai Hospital, Navy Medical University, Shanghai, China.
Jinhong HuDepartment of Pharmacy, Changhai Hospital, Navy Medical University, Shanghai, China.
Jiyong LiuDepartment of Pharmacy, Fudan University Shanghai Cancer Center, Shanghai, China.
Changhai Hospital · CNChinese People's Liberation Army · CNSecond Military Medical University · CNShanghai Medical Information Center · CNShanghai Stomatological Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: As a key chemotactic factor during Eos recruitment on the allergic inflammation site, eotaxin is regarded as one of the important therapeutic targets. Aim: To address the expression and regulation mechanism of eotaxin, which constitutes an important procedure in skin allergic disease and a target for drug therapy. Material and methods: An allergic contact dermatitis (ACD) model of mouse was established. Immunohistochemical method (ICH) and flow cytometry method (FCM) were used to determine the amounts of CD4+ and CD8+ T cells and their ratios. The eotaxin mRNA and protein were evaluated by real-time PCR, ICH and western-blotting method. Nuclear factor-κB (NF-κB) nuclear translocation and STAT6 phosphorylation were studied by EMSA and western-blotting methods. Results: We confirmed that both CD4+ and CD8+ T cells in mouse blood and tissue increased during the allergic process, FBs was the main source for eotaxin under the allergic condition. Both TNF-α and IL-4 showed synergic effects on the up-regulation of eotaxin mRNA and protein in KC and FBs. Eotaxin can be expressed via NF-κB and STAT6 transcription after KC and FBs were stimulated by TNF-α and IL-4. Conclusions: The obvious up-regulation of eotaxin expression in skin tissue of the mouse ACD model was confirmed, the exact expression site and dynamic process was determined both in vivo and in vitro. The eotaxin expression ability of FBs outperformed that of KC, and eotaxin expression can be regulated by TNF-α and IL-4 via NF-κB and STAT6. The overall findings may pave the way for discovering targets for new drugs and new therapeutic drugs for treating allergic diseases.

Indexed as

allergyeotaxinfibroblastkeratinocyteskin

Identifiers

PMID35950112
PMCPMC9326924
OpenAlexW4285611870

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.