Evidence map›Paper›PMID 39654684›Full record

ReviewMedComm2024

Atopic dermatitis: pathogenesis and therapeutic intervention.

Chengcheng Yue, Hong Zhou, Xiaoyan Wang, Jiadong Yu, Yawen Hu, Pei Zhou, Fulei Zhao, Fanlian Zeng, Guolin Li, Ya Li and 7 more

Abstract readReview
In one paragraph

Review in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  16. Chaga Mushroom (Journal of microbiology and biotechnology · 2026
    Article
  17. Skin examination in extreme conditions.Acta biochimica Polonica · 2026
    Review
  18. Article
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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

17 authors.

Chengcheng YueState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.ORCID https://orcid.org/0000-0001-6093-5615
Hong ZhouState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Xiaoyan WangState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Jiadong YuState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Yawen HuState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Pei ZhouState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Fulei ZhaoState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Fanlian ZengState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Guolin LiState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Ya LiState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Yuting FengState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Xiaochi SunDepartment of Cardiology West China Hospital Sichuan University Chengdu Sichuan China.
Shishi HuangState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Mingxiang HeState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Wenling WuState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Nongyu HuangState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.
Jiong LiState Key Laboratory of Biotherapy and Cancer Center West China Hospital Sichuan University Sichuan University and Collaborative Innovation Center for Biotherapy Chengdu Sichuan China.ORCID https://orcid.org/0000-0003-2320-9387

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The skin serves as the first protective barrier for nonspecific immunity and encompasses a vast network of skin-associated immune cells. Atopic dermatitis (AD) is a prevalent inflammatory skin disease that affects individuals of all ages and races, with a complex pathogenesis intricately linked to genetic, environmental factors, skin barrier dysfunction as well as immune dysfunction. Individuals diagnosed with AD frequently exhibit genetic predispositions, characterized by mutations that impact the structural integrity of the skin barrier. This barrier dysfunction leads to the release of alarmins, activating the type 2 immune pathway and recruiting various immune cells to the skin, where they coordinate cutaneous immune responses. In this review, we summarize experimental models of AD and provide an overview of its pathogenesis and the therapeutic interventions. We focus on elucidating the intricate interplay between the immune system of the skin and the complex regulatory mechanisms, as well as commonly used treatments for AD, aiming to systematically understand the cellular and molecular crosstalk in AD-affected skin. Our overarching objective is to provide novel insights and inform potential clinical interventions to reduce the incidence and impact of AD.

Indexed as

atopic dermatitisimmune cellspathophysiologytherapeutic intervention

Identifiers

PMID39654684
PMCPMC11625510

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.