Evidence map›Paper›PMID 29143918›Full record

ArticleImmunologic research2018

Induction of CD4

Maryam Khosravi, Ali Bidmeshkipour, Ali Moravej, Suzzan Hojjat-Assari, Sina Naserian, Mohammad Hossein Karimi

Abstract read
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In one paragraph

Article in Immunologic research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  9. Mesodermal Derivatives of Pluripotent Stem Cells Route to Scarless Healing.International journal of molecular sciences · 2023
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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

6 authors at 5 institutions in 2 countries.

Maryam KhosraviTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Ali BidmeshkipourDepartment of Biology, Faculty of Science, Razi University, Kermanshah, Iran. a.bidmeshkipour@gmail.com.
Ali MoravejNoncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Suzzan Hojjat-AssariInstitut Français de Recherche et d'Enseignement Supérieur à l'International (IFRES-INT), Paris, France.
Sina NaserianInserm, U1197, Hôpital Paul Brousse, 94807, Villejuif, France.
Mohammad Hossein KarimiTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. Karimimh@sums.ac.ir.
Razi University · IRFasa University of Medical Sciences · IRInserm · FRInstitut Français des Relations Internationales · FRShiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among the particular immunomodulation properties of mesenchymal stem cells (MSCs), one relies on their capacity to regulatory T cell (Treg) induction from effector T cells. Stable expression of Foxp3 has a dominant role in suppressive phenotype and stability of induced regulatory T cells (iTregs). How MSCs induce stable Foxp3 expression in iTregs remains unknown. We previously showed MSCs could enhance demethylation of Treg-specific demethylated region (TSDR) in iTregs in cell-cell contact manner (unpublished data). Here, we evaluated the possible effect of MSCs on the mRNA expression of Runx complex genes (Runx1, Runx3, and CBFB) that perch on TSDR in iTregs and play the main role in suppressive properties of Tregs, a regulatory pathway that has not yet been explored by MSCs. Also, we investigated the mRNA expression of MBD2 that promotes TSDR demethylation in Tregs. We first showed that in vitro MSC-iTreg induction was associated with strong mRNA modifications of genes involved in Runx complex. We next injected high doses of MSCs in a murine model of C57BL/6 into Balb/C allogeneic skin transplantation to prolong allograft survival. When splenocytes of grafted mice were analyzed, we realized that the Foxp3 expression was increased at day 5 and 10 post-graft merely in MSC-treated mice. Furthermore, Foxp3 mRNA expression was associated with modified Runx complex mRNA expression comparable to what was shown in in vitro studies. Hence, our data identify a possible mechanism in which MSCs convert conventional T cells to iTreg through strong modifications of mRNA of genes that are involved in Runx complex of Foxp3.

Indexed as

AnimalsCD4 AntigensCell DifferentiationCells, CulturedCore Binding Factor alpha SubunitsDNA-Binding ProteinsDNA MethylationFemaleForkhead Transcription FactorsGene Expression RegulationInterleukin-2 Receptor alpha SubunitLymphocyte ActivationMesenchymal Stem CellsMiceMice, Inbred BALB CMice, Inbred C57BLCD4 AntigensCore Binding Factor alpha SubunitsDNA-Binding ProteinsForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-2 Receptor alpha SubunitMbd2 protein, mouseRNA, MessengerDemethylationMesenchymal stem cellsRegulatory T cellsRunx complex

Identifiers

PMID29143918
OpenAlexW2770567643

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.