Evidence map›Paper›PMID 38512654›Full record

ArticleInflammopharmacology2024

Synergistic effects of mesenchymal stem cell-derived extracellular vesicles and dexamethasone on macrophage polarization under inflammatory conditions.

Zahra Mirsanei, Fatemeh Jamshidi-Adegani, Saeid Vakilian, Fateme Ahangari, Sara Soufihasanabad, Khamis Al-Riyami, Sara Soudi, Sahar Ghaffari Khaligh, Sulaiman Al-Hashmi, Seyed Mahmoud Hashemi

Abstract read
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In one paragraph

Article in Inflammopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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  5. Developing anACS pharmacology & translational science · 2025
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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 5 institutions in 2 countries.

Zahra MirsaneiDepartment of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Fatemeh Jamshidi-AdeganiLaboratory for Stem Cell and Regenerative Medicine, Natural and Medical Sciences Research Center, University of Nizwa, P. O. Box: 33, PC, 616, Nizwa, Oman.
Saeid VakilianLaboratory for Stem Cell and Regenerative Medicine, Natural and Medical Sciences Research Center, University of Nizwa, P. O. Box: 33, PC, 616, Nizwa, Oman.
Fateme AhangariDepartment of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Sara SoufihasanabadDepartment of Biology, School of Natural Sciences, University of Tabriz, Tabriz, Iran.
Khamis Al-RiyamiLaboratory for Stem Cell and Regenerative Medicine, Natural and Medical Sciences Research Center, University of Nizwa, P. O. Box: 33, PC, 616, Nizwa, Oman.
Sara SoudiDepartment of Immunology, Faculty of Medical Sciences, Tarbiat Modarres University, Tehran, Iran.
Sahar Ghaffari KhalighDepartment of Pathology, Veterinary Faculty, Semnan University, Semnan, Iran.
Sulaiman Al-HashmiLaboratory for Stem Cell and Regenerative Medicine, Natural and Medical Sciences Research Center, University of Nizwa, P. O. Box: 33, PC, 616, Nizwa, Oman. sahashmi@unizwa.edu.om.ORCID http://orcid.org/0000-0002-4010-116X
Seyed Mahmoud HashemiDepartment of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. smmhashemi@sbmu.ac.ir.ORCID http://orcid.org/0000-0003-1389-5803
University of Nizwa · OMShahid Beheshti University of Medical Sciences · IRSemnan University · IRTarbiat Modares University · IRUniversity of Tabriz · IR

Funding

Shahid Beheshti University of Medical Sciences 43006101University of Nizwa BFP/RGP/HSS/21/037
6 · The paper itself

Abstract

The undesirable inflammation and the excessive M1 macrophage activity may lead to inflammatory diseases. Corticosteroids and stem cell therapy are used in clinical practice to promote anti-inflammatory responses. However, this protocol has limitations and is associated with numerous side effects. In this study, the synergistic anti-inflammatory effects of dexamethasone (Dex) and mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) were evaluated to enhance the polarization of M1 inflammatory macrophages into the anti-inflammatory (M2) phenotype. Hence, we designed different combinations of Dex and EVs using three methods, including EVs isolated from Dex-preconditioned MSCs (Pre-Dex-EVs), EVs loaded with Dex (L-Dex-EVs), and EVs and Dex co-administration (Dex + EVs). All designed EVs had a significant effect on reducing the expression of M1-related genes (iNOS, Stat1, and IRF5), cytokines (IL6 and TNF-a), and CD markers (CD86) in lipopolysaccharide-stimulated macrophages. On the other hand, these combinations promoted the expression of alternative-activated M2-related genes (Arg-1, Stat6, and IRF4), cytokine (IL10), and CD markers (CD206).The combination of Dex and MSC-EVs enhances the effectiveness of both and synergistically promotes the conversion of inflammatory macrophages into an anti-inflammatory state.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsAnti-Inflammatory AgentsCytokinesDexamethasoneMacrophagesAnti-Inflammatory AgentsCytokinesDexamethasoneDexamethasoneExtracellular VesicleInflammationMacrophage PolarizationMesenchymal Stem CellSynergistic Effects

Identifiers

PMID38512654
OpenAlexW4393036588

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.