Evidence map›Paper›PMID 31227956›Full record

ArticleInflammation2019

Therapeutic Effects of Mesenchymal Stem Cells Derived From Bone Marrow, Umbilical Cord Blood, and Pluripotent Stem Cells in a Mouse Model of Chemically Induced Inflammatory Bowel Disease.

Argyro Kagia, Maria Tzetis, Emmanuel Kanavakis, Despina Perrea, Irene Sfougataki, Anny Mertzanian, Ioanna Varela, Aikaterini Dimopoulou, Angeliki Karagiannidou, Evgenios Goussetis

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  8. The application potential of iMSCs and iMSC-EVs in diseases.Frontiers in bioengineering and biotechnology · 2024
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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

10 authors at 4 institutions in 1 country.

Argyro KagiaObstetric and Gynecological Department, General Hospital of Athens "Konstantopouleio", Nea Ionia, Greece. argiro.kagia@gmail.com.ORCID http://orcid.org/0000-0002-4356-571X
Maria TzetisFaculty of Medicine, Department of Genetics, Medical School, National & Kapodistrian University of Athens, Athens, Greece.
Emmanuel KanavakisFaculty of Medicine, Department of Genetics, Medical School, National & Kapodistrian University of Athens, Athens, Greece.
Despina PerreaLaboratory of Experimental Surgery and Surgical Research "Christeas Hall", Medical School, National & Kapodistrian University of Athens, Athens, Greece.
Irene SfougatakiStem Cell Transplant Unit, Aghia Sophia Children's Hospital of Athens, Athens, Greece.
Anny MertzanianStem Cell Transplant Unit, Aghia Sophia Children's Hospital of Athens, Athens, Greece.
Ioanna VarelaStem Cell Transplant Unit, Aghia Sophia Children's Hospital of Athens, Athens, Greece.
Aikaterini DimopoulouHistopathological Department, "Helena Venizelou" Gynecological Hospital, Athens, Greece.
Angeliki KaragiannidouStem Cell Transplant Unit, Aghia Sophia Children's Hospital of Athens, Athens, Greece.
Evgenios GoussetisStem Cell Transplant Unit, Aghia Sophia Children's Hospital of Athens, Athens, Greece.
Children's Hospital Agia Sophia · GRNational and Kapodistrian University of Athens · GRAgia Olga Hospital · GRGeneral-Maternity District Hospital Helena Venizelou · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute inflammatory bowel disease (AIBD) is a wide clinical entity including severe gastrointestinal pathologies with common histopathological basis. Epidemiologically increasing diseases, such as necrotizing enterocolitis (NEC), gastrointestinal graft versus host disease (GVHD), and the primary acute phase of chronic inflammatory bowel disease (CIBD), exhibit a high necessity for new therapeutic strategies. Mesenchymal stem cell (MSC) cellular therapy represents a promising option for the treatment of these diseases. In our study, we comparatively assess the efficacy of human MSCs derived from bone marrow (BM), umbilical cord blood (UCB), human embryonic stem cells (ESCs), or human-induced pluripotent stem cells (iPSCs) in a mouse model of chemically induced acute enterocolitis. The laboratory animals were provided ad libitum potable dextrane sulfate sodium solution (DSS) in order to reproduce an AIBD model and then individually exposed intraperitoneally to MSCs derived from BM (BM-MSCs), UCB (UCB-MSCs), ESCs (ESC-MSCs), or iPSCs (iPSC-MSCs). The parameters used to evaluate the cellular treatment efficacy were the animal survival prolongation and the histopathological-macroscopic picture of bowel sections. Although all categories of mesenchymal stem cells led to statistically significant survival prolongation compared to the control group, significant clinical and histopathological improvement was observed only in mice receiving BM-MSCs and UCB-MSCs. Our results demonstrated that the in vivo anti-inflammatory effect of ESC-MSCs and iPSC-MSCs was inferior to that of UCB-MSCs and BM-MSCs. Further investigation will clarify the potential of ESCs and iPSC-derived MSCs in AIBD treatment.

Indexed as

AnimalsBone Marrow CellsDisease Models, AnimalFetal BloodHumansInduced Pluripotent Stem CellsInflammatory Bowel DiseasesMesenchymal Stem Cell TransplantationMiceSurvival Analysisanimal modelbowel diseaseintraperitonealmesenchymal stem cellspluripotent

Identifiers

PMID31227956
OpenAlexW2949182069

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.