Evidence map›Paper›PMID 38067171›Full record

ArticleCells2023

The Potential of Mesenchymal Stem/Stromal Cell Therapy in Mustard Keratopathy: Discovering New Roads to Combat Cellular Senescence.

Mohammad Soleimani, Arash Mirzaei, Kasra Cheraqpour, Seyed Mahbod Baharnoori, Zohreh Arabpour, Mohammad Javad Ashraf, Mahmood Ghassemi, Ali R Djalilian

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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 2 countries.

Mohammad SoleimaniEye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran 1336616351, Iran.ORCID 0000-0002-6546-3546
Arash MirzaeiEye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran 1336616351, Iran.
Kasra CheraqpourEye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran 1336616351, Iran.ORCID 0000-0002-1273-9166
Seyed Mahbod BaharnooriDepartment of Ophthalmology and Visual Sciences, University of Illinois, Chicago, IL 60612, USA.
Zohreh ArabpourDepartment of Ophthalmology and Visual Sciences, University of Illinois, Chicago, IL 60612, USA.
Mohammad Javad AshrafDepartment of Ophthalmology and Visual Sciences, University of Illinois, Chicago, IL 60612, USA.
Mahmood GhassemiDepartment of Ophthalmology and Visual Sciences, University of Illinois, Chicago, IL 60612, USA.ORCID 0000-0002-9275-3813
Ali R DjalilianDepartment of Ophthalmology and Visual Sciences, University of Illinois, Chicago, IL 60612, USA.
University of Illinois Urbana-Champaign · USFarabi Hospital · IR

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MCANANY, JAMES JASON · 1985 to 2025
$14.8M
Novel Therapies for Ocular Chemical InjuriesR01EY024349 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DJALILIAN, ALI R · 2015 to 2020
$2.1M
Phase I Study of Mesenchymal Stromal Cell Secretome for Promoting Corneal RegenerationUH3EY031809 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ALI R DJALILIAN · 2021 to 2026
$1.6M
NEI NIH HHS P30 EY001792NEI NIH HHS R01 EY024349NEI NIH HHS UH3 EY031809
6 · The paper itself

Abstract

Mesenchymal stem/stromal cells (MSCs) are considered a valuable option to treat ocular surface disorders such as mustard keratopathy (MK). MK often leads to vision impairment due to corneal opacification and neovascularization and cellular senescence seems to have a role in its pathophysiology. Herein, we utilized intrastromal MSC injections to treat MK. Thirty-two mice were divided into four groups based on the exposure to 20 mM or 40 mM concentrations of mustard and receiving the treatment or not. Mice were clinically and histopathologically examined. Histopathological evaluations were completed after the euthanasia of mice after four months and included hematoxylin and eosin (H&E), CK12, and beta-galactosidase (β-gal) staining. The treatment group demonstrated reduced opacity compared to the control group. While corneal neovascularization did not display significant variations between the groups, the control group did register higher numerical values. Histopathologically, reduced CK12 staining was detected in the control group. Additionally, β-gal staining areas were notably lower in the treatment group. Although the treated groups showed lower severity of fibrosis compared to the control groups, statistical difference was not significant. In conclusion, it seems that delivery of MSCs in MK has exhibited promising therapeutic results, notably in reducing corneal opacity. Furthermore, the significant reduction in the β-galactosidase staining area may point towards the promising anti-senescence potential of MSCs.

Indexed as

Mesenchymal Stem CellsMustard PlantAnimalsbeta-GalactosidaseCellular SenescenceMicebeta-Galactosidaseintrastromalmesenchymal stem/stromal cellsMSCsmustardmustard keratopathynitrogen mustardocular surfacesenescencetreatment

Identifiers

PMID38067171
PMCPMC10705954
OpenAlexW4389190198

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.