Evidence map›Paper›PMID 41179646›Full record

ReviewArchives of Razi Institute2025

Immunomodulatory Functions of Mesenchymal Stem Cells in Tissue Engineering.

Hosseini Amirhossein, Abdolmaleki Arash, Nahumi Aida, Asadi Asadollah, Ghanimi Hussein A

Abstract readReview
In one paragraph

Review in Archives of Razi Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

5 authors.

Hosseini AmirhosseinDepartment of Biology, Faculty of Science, University of Mohaghegh Ardabili, Ardabil, Iran.
Abdolmaleki ArashDepartment of Biophysics, Faculty of Advanced Technologies, University of Mohaghegh Ardabili, Namin, Iran.
Nahumi AidaDepartment of Biology, Faculty of Science, University of Mohaghegh Ardabili, Ardabil, Iran.
Asadi AsadollahDepartment of Biology, Faculty of Science, University of Mohaghegh Ardabili, Ardabil, Iran.
Ghanimi Hussein ACollege of Nursing, University of Al-Ameed, Karbala, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have been demonstrated to exhibit immunomodulatory properties, thereby modulating the immune response and facilitating tissue regeneration. These properties include the ability to suppress T cell proliferation, modulate macrophage polarization, and promote regulatory T cell differentiation. It has been demonstrated that natural chemoattraction pathways can attract MSCs. These cells are created from around the injured tissues, creating a repair/regenerative microenvironment for this study. The rate of tissue regeneration is contingent upon factors such as the patient's age, the extent of tissue damage, and the specific anatomical region affected. It has been demonstrated that the manipulation of mesenchymal stem cells can exert a substantial influence on the rate of tissue damage, tissue regeneration, and cell death. The immunosuppressive and trophic mechanisms under investigation are distinct from the mechanisms that are being led by tissue engineering to replace special mesenchymal tissues. Indeed, the capacity of tissue engineering processes to facilitate trophic interactions is evident, thereby promoting remarkable tissue regeneration and ensuring the seamless incorporation of newly generated tissue into the body. The field of MSCs has been a subject of study for over two decades, and recent advancements have begun to unlock their full potential for clinical applications. It is evident that the utilization of MSCs in tissue engineering necessitates distinct rationale when compared to their application in nutritional and immunomodulatory functions. These latter efforts now appear to apply to the clinic before tissue engineering methods become feasible. The findings of this study demonstrate that MSCs possess the capacity to differentiate into various cell types, which renders them a suitable candidate for treating a wide range of human diseases.

Indexed as

ImmunomodulationMesenchymal Stem CellsTissue EngineeringAnimalsHumansBone MarrowImmunomodulationMacrophageMesenchymal Stem CellsTissue Engineering

Identifiers

PMID41179646
PMCPMC12572674

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.