Evidence map›Paper›PMID 40353645›Full record

ReviewImmunity, inflammation and disease2025

Clinical Progress in Mesenchymal Stem Cell Therapy: A Focus on Rheumatic Diseases.

Helal F Hetta, Alaa Elsaghir, Victor Coll Sijercic, Abdulrahman K Ahmed, Sayed A Gad, Mahlet S Zeleke, Fawaz E Alanazi, Yasmin N Ramadan

Abstract readReview
In one paragraph

Review in Immunity, inflammation and disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
–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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. 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

8 authors.

Helal F HettaDivision of Microbiology, Immunology and Biotechnology, Department of Natural Products and Alternative Medicine, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.ORCID 0000-0001-8541-7304
Alaa ElsaghirDepartment of Microbiology and Immunology, Faculty of Pharmacy, Assiut University, Assiut, Egypt.ORCID 0000-0002-8881-3545
Victor Coll SijercicNorth Central College, Naperville, Illinois, USA.
Abdulrahman K AhmedEmergency Medicine Unit, Department of Anaethesia and Intensive Care, Faculty of Medicine, Assiut University, Assiut, Egypt.ORCID 0000-0002-5134-1089
Sayed A GadEmergency Medicine Unit, Department of Anaethesia and Intensive Care, Faculty of Medicine, Assiut University, Assiut, Egypt.
Mahlet S ZelekeMenelik II Medical and Health Science College, Addis Ababa, Ethiopia.ORCID 0009-0005-0766-3055
Fawaz E AlanaziDepartment of Pharmacology and Toxicology, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.ORCID 0000-0002-8353-2066
Yasmin N RamadanDepartment of Microbiology and Immunology, Faculty of Pharmacy, Assiut University, Assiut, Egypt.ORCID 0009-0008-7374-9334

Funding

The authors received no specific funding for this work.
6 · The paper itself

Abstract

backgroundRheumatic diseases are chronic immune-mediated disorders affecting multiple organ systems and significantly impairing patients' quality of life. Current treatments primarily provide symptomatic relief without offering a cure. Mesenchymal stem cells (MSCs) have emerged as a promising therapeutic option due to their ability to differentiate into various cell types and their immunomodulatory, anti-inflammatory, and regenerative properties. This review aims to summarize the clinical progress of MSC therapy in rheumatic diseases, highlight key findings from preclinical and clinical studies, and discuss challenges and future directions. METHODOLOGY: A comprehensive review of preclinical and clinical studies on MSC therapy in rheumatic diseases, including systemic lupus erythematosus, rheumatoid arthritis, ankylosing spondylitis, osteoarthritis, osteoporosis, Sjögren's syndrome, Crohn's disease, fibromyalgia, systemic sclerosis, dermatomyositis, and polymyositis, was conducted. Emerging strategies to enhance MSC efficacy and overcome current limitations were also analyzed. RESULTS AND DISCUSSION: Evidence from preclinical and clinical studies suggests that MSC therapy can reduce inflammation, modulate immune responses, and promote tissue repair in various rheumatic diseases. Clinical trials have demonstrated potential benefits, including symptom relief and disease progression delay. However, challenges such as variability in treatment response, optimal cell source and dosing, long-term safety concerns, and regulatory hurdles remain significant barriers to clinical translation. Standardized protocols and further research are required to optimize MSC application.

conclusionMSC therapy holds promise for managing rheumatic diseases, offering potential disease-modifying effects beyond conventional treatments. However, large-scale, well-controlled clinical trials are essential to establish efficacy, safety, and long-term therapeutic potential. Addressing current limitations through optimized treatment protocols and regulatory frameworks will be key to its successful integration into clinical practice.

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationRheumatic DiseasesAnimalsClinical Trials as TopicHumansmesenchymal stem cellsosteoarthritisrheumatic diseasesrheumatoid arthritissystemic lupus erythematosussystemic sclerosis

Identifiers

PMID40353645
PMCPMC12067559

What Socratic 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 Socratic graph.