Evidence map›Paper›PMID 32734446›Full record

ArticleImmunologic research2020

Comparative study between human mesenchymal stem cells and etanercept as immunomodulatory agents in rat model of rheumatoid arthritis.

Heba El-Gendy, Salah El-Deen Hawass, Manal Awad, Mona Ahmad Mohsen, Maha Amin, Hussein Abdelaziz Abdalla, Samah Fouad, Ahmed Lotfy

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Immunologic research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  5. Stem cell therapies for autoimmune hepatitis.Stem cell research & therapy · 2021
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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

8 authors at 2 institutions in 1 country.

Heba El-GendyDepartment of Rheumatology and Rehabilitation, Faculty of Medicine, Mansoura University, Mansoura, Egypt. hebamd31@gmail.com.ORCID 0000-0002-3528-6825
Salah El-Deen HawassDepartment of Rheumatology and Rehabilitation, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Manal AwadDepartment of Rheumatology and Rehabilitation, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mona Ahmad MohsenDepartment of Rheumatology and Rehabilitation, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Maha AminDepartment of Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Hussein Abdelaziz AbdallaDepartment of Biochemistry, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Samah FouadMedical Experimental Research Centre , Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Ahmed LotfyeBiotechnology and Life Sciences Department, Faculty of Postgraduate Studies for Advanced Sciences (PSAS), Beni-Suef University, Beni-Suef, Egypt.
Mansoura University · EGBeni-Suef University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To compare human adipose tissue mesenchymal stem cells (AT-MSCs) and etanercept as immunomodulatory agents for collagen-induced arthritis (CIA). CIA was induced by rats' immunization with collagen type II (CII) in complete Freund's adjuvant in days 0 and 7. Before the onset of CIA, prevention group received five doses of AT-MSCS intraperitoneally. After establishment of arthritis, rats received either five doses of AT-MSCs or phosphate-buffered saline (PBS) intraperitoneally or six doses of etanercept subcutaneously. Clinical and histopathological evaluation were performed in all groups; serum levels of tumor necrosis factor-α (TNF-α), interleukin-10 (IL-10), and anti-collagen II were assessed by enzyme-linked immunosorbent assay (ELISA). A total percent of autoreactive T and regulatory T (Treg) cells were quantified using spleen immune histochemical analysis. AT-MSCs were able to delay the onset of CIA, suppress the ongoing clinical and histopathological signs, decrease serum levels of TNF-α and anti-collagen type II, and downregulate the autoreactive T cells as etanercept. AT-MSCs were more potent in Treg cells upregulation, producing high serum levels of IL10. AT-MSCs might have a therapeutic effect in CIA via their potency in immune cell education, representing an effective new promising approach in rheumatoid arthritis in human.

Indexed as

Mesenchymal Stem Cell TransplantationAdipose TissueAnimalsAntirheumatic AgentsArthritis, ExperimentalArthritis, RheumatoidCollagen Type IIEtanerceptFemaleFreund's AdjuvantHumansInterleukin-10RatsT-Lymphocytes, RegulatoryTumor Necrosis Factor-alphaAntirheumatic AgentsCollagen Type IIEtanerceptFreund's AdjuvantInterleukin-10Tumor Necrosis Factor-alphaCIAEtanerceptMesenchymal stem cellsRegulatory T cellsRheumatoid arthritis

Identifiers

PMID32734446
OpenAlexW3046713541

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.