Evidence map›Paper›PMID 38003230›Full record

ReviewInternational journal of molecular sciences2023

Mesenchymal Stem Cells in the Pathogenesis and Therapy of Autoimmune and Autoinflammatory Diseases.

Lina N Zaripova, Angela Midgley, Stephen E Christmas, Michael W Beresford, Clare Pain, Eileen M Baildam, Rachel A Oldershaw

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 2 pooled it
22.7field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 2 syntheses or guidelines pooled it, 79 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
  5. Mesenchymal Stromal Cell-Based Cell-Drug Conjugates for the Treatment of Acute Liver Failure.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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14 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Lina N ZaripovaInstitute of Fundamental and Applied Medicine, National Scientific Medical Center, 42 Abylai Khan Avenue, Astana 010000, Kazakhstan.ORCID 0000-0001-8728-0225
Angela MidgleyDepartment of Women and Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool, Institute in the Park, Alder Hey Children's NHS Foundation Trust, Liverpool L14 5AB, UK.
Stephen E ChristmasDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection and Global Health, Faculty of Health and Life Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby Street, Liverpool L69 7BE, UK.
Michael W BeresfordDepartment of Women and Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool, Institute in the Park, Alder Hey Children's NHS Foundation Trust, Liverpool L14 5AB, UK.
Clare PainDepartment of Women and Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool, Institute in the Park, Alder Hey Children's NHS Foundation Trust, Liverpool L14 5AB, UK.
Eileen M BaildamDepartment of Paediatric Rheumatology, The Alexandra Hospital, Mill Lane, Cheadle SK8 2PX, UK.
Rachel A OldershawDepartment of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, Faculty of Health and Life Sciences, University of Liverpool, William Henry Duncan Building, 6 West Derby Street, Liverpool L7 8TX, UK.ORCID 0000-0001-8478-599X
University of Liverpool · GBAlexandra Hospital · GB

Funding

Wellcome Trust 097826/z/11/z
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) modulate immune responses and maintain self-tolerance. Their trophic activities and regenerative properties make them potential immunosuppressants for treating autoimmune and autoinflammatory diseases. MSCs are drawn to sites of injury and inflammation where they can both reduce inflammation and contribute to tissue regeneration. An increased understanding of the role of MSCs in the development and progression of autoimmune disorders has revealed that MSCs are passive targets in the inflammatory process, becoming impaired by it and exhibiting loss of immunomodulatory activity. MSCs have been considered as potential novel cell therapies for severe autoimmune and autoinflammatory diseases, which at present have only disease modifying rather than curative treatment options. MSCs are emerging as potential therapies for severe autoimmune and autoinflammatory diseases. Clinical application of MSCs in rare cases of severe disease in which other existing treatment modalities have failed, have demonstrated potential use in treating multiple diseases, including rheumatoid arthritis, systemic lupus erythematosus, myocardial infarction, liver cirrhosis, spinal cord injury, multiple sclerosis, and COVID-19 pneumonia. This review explores the biological mechanisms behind the role of MSCs in autoimmune and autoinflammatory diseases. It also covers their immunomodulatory capabilities, potential therapeutic applications, and the challenges and risks associated with MSC therapy.

Indexed as

Autoimmune DiseasesHereditary Autoinflammatory DiseasesMesenchymal Stem CellsMesenchymal Stem Cell TransplantationHumansImmune ToleranceImmunomodulationInflammationallogeneic stem cellsautoimmuneautoinflammatoryautologous mesenchymal stem cellsimmunogenicityimmunomodulationmesenchymal stem cell dysfunctionmesenchymal stem cellsmesenchymal stem cell transplantation

Identifiers

PMID38003230
PMCPMC10671211
OpenAlexW4388464826

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.