Evidence map›Paper›PMID 39224661›Full record

ReviewJournal of inflammation research2024

Therapeutic Potential and Mechanisms of Mesenchymal Stem Cell and Mesenchymal Stem Cell-Derived Extracellular Vesicles in Atopic Dermatitis.

Kang He, Jie Zang, Tingting Ren, Shaojie Feng, Mohan Liu, Xude Zhang, Wenchang Sun, Jinjin Chu, Donghua Xu, Fengxia Liu

Abstract readReview
In one paragraph

Review in Journal of inflammation research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. 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

10 authors.

Kang He *Department of Clinical Medicine of Shandong Second Medical University, Weifang, People's Republic of China.
Jie Zang *Central Laboratory, Weifang People's Hospital, Shandong Second Medical University/Weifang People's Hospital, Weifang, People's Republic of China.
Tingting Ren *Department of Clinical Medicine of Shandong Second Medical University, Weifang, People's Republic of China.
Shaojie FengDepartment of Allergy, Weifang People's Hospital, Shandong Second Medical University, Weifang, People's Republic of China.
Mohan LiuDepartment of Clinical Medicine of Shandong Second Medical University, Weifang, People's Republic of China.
Xude ZhangDepartment of Allergy, Weifang People's Hospital, Shandong Second Medical University, Weifang, People's Republic of China.
Wenchang SunCentral Laboratory, Weifang People's Hospital, Shandong Second Medical University/Weifang People's Hospital, Weifang, People's Republic of China.
Jinjin ChuCentral Laboratory, Weifang People's Hospital, Shandong Second Medical University/Weifang People's Hospital, Weifang, People's Republic of China.
Donghua XuCentral Laboratory, Weifang People's Hospital, Shandong Second Medical University/Weifang People's Hospital, Weifang, People's Republic of China.
Fengxia LiuDepartment of Allergy, Weifang People's Hospital, Shandong Second Medical University, Weifang, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atopic dermatitis (AD) is a chronic and inflammatory skin disease with intense itchiness that is highly prevalent worldwide.The pathogenesis of AD is complex and closely related to genetic factors, immunopathogenic factors, environmental factors, and skin infections. Mesenchymal stem cells (MSCs) are non-hematopoietic progenitor cells derived from the mesenchymal stroma. They have anti-inflammatory, anti-apoptotic, and regenerative properties. Numerous studies demonstrate that MSCs can play a therapeutic role in AD by regulating various immune cells, maintaining immune homeostasis, and promoting the repair of damaged tissues. The key mediators for their biological functions are extracellular vesicles (MSC-Evs) and soluble cytokines derived from MSCs. The safety and efficacy of MSCs have been demonstrated in clinical Phase I / IIa trials for AD. This paper provides a comprehensive review of the pathogenesis of AD and the currently published studies on the function of MSCs and MSC-Evs in AD, primarily including the pathogenesis and the immunomodulatory impacts of MSCs and MSC-Evs, along with advancements in clinical studies. It provides insights for comprehending AD pathogenesis and investigating treatments based on MSCs.

Indexed as

atopic dermatitisextracellular vesiclemesenchymal stem cellsTh2-associated immunity

Identifiers

PMID39224661
PMCPMC11368146

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.