Evidence map›Paper›PMID 32707035›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2020

B7-H1 Promotes the Functional Effect of Human Gingiva-Derived Mesenchymal Stem Cells on Collagen-Induced Arthritis Murine Model.

Wenbin Wu, Ze Xiu Xiao, Donglan Zeng, Feng Huang, Julie Wang, Yanying Liu, Joseph A Bellanti, Nancy Olsen, Song Guo Zheng

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

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  16. Cell-based therapies for rheumatoid arthritis: opportunities and challenges.Therapeutic advances in musculoskeletal disease · 2022
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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

9 authors at 6 institutions in 2 countries.

Wenbin WuDepartment of Clinical Immunology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.
Ze Xiu XiaoDepartment of Clinical Immunology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.
Donglan ZengDepartment of Clinical Immunology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.
Feng HuangDepartment of Clinical Immunology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.
Julie WangDepartment of Internal Medicine, Ohio State University College of Medicine and Wexner Medical Center, Columbus, OH 43210, USA.
Yanying LiuDepartment of Rheumatology & Immunology, Peking University People's Hospital, Beijing 100044, China.
Joseph A BellantiDepartments of Pediatrics and Microbiology-Immunology and the International Center for Interdisciplinary Studies of Immunology (ICISI), Georgetown University Medical Center, Washington, DC 20057, USA.
Nancy OlsenDepartment of Medicine, Penn State University Hershey Medical Center, Hershey, PA 17033, USA.
Song Guo ZhengDepartment of Internal Medicine, Ohio State University College of Medicine and Wexner Medical Center, Columbus, OH 43210, USA. Electronic address: songguozheng2013@yahoo.com.
Sun Yat-sen University · CNThe Ohio State University Wexner Medical Center · USThird Affiliated Hospital of Sun Yat-sen University · CNGeorgetown University Medical Center · USPeking University People's Hospital · CNPenn State Milton S. Hershey Medical Center · US

Funding

Mesenchymal Stem Cells Derived from Human Gingiva (GMSC) Inhibit Bone Erosion in Autoimmune ArthritisR61AR073049 · NIAMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI ZHENG, SONG GUO · 2017 to 2018
$767k
NIAMS NIH HHS R61 AR073049
6 · The paper itself

Abstract

Recent studies found that mesenchymal stem cells (MSCs), by virtue of their tissue recovery and immunoregulatory properties, have shown a broad prospect for applications in various autoimmune and degenerative diseases. Although the potential therapeutic use of MSCs is considerable, studies and clinical treatment efficacy are preliminary due to the heterogeneity of MSCs. Herein, based on RNA-sequencing (RNA-seq) and single cell sequence properties, we demonstrated that B7-H1 plays an important role in the immunosuppressive function of human gingiva-derived mesenchymal stem cells (GMSCs) in a collagen-induced arthritis murine model that is dependent on STAT3 signaling. Our data offer convincing evidence that B7-H1 expression by GMSCs helps to identify a new subpopulation of MSCs with a greater immunosuppressive property. The approach provides a unique and additional strategy for stem cells-based therapies of autoimmune and other inflammatory diseases.

Indexed as

AnimalsArthritis, ExperimentalAutoimmunityB7-H1 AntigenBiomarkersCollagenDisease Models, AnimalDisease SusceptibilityGingivaHumansMesenchymal Stem CellsMiceSignal TransductionSTAT3 Transcription FactorB7-H1 AntigenBiomarkersCD274 protein, humanCollagenSTAT3 Transcription FactorB7-H1GMSCimmunoregulatoryRASTAT3

Identifiers

PMID32707035
PMCPMC7646216
OpenAlexW3038440059

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.