Preclinical stem cell therapy in fetuses with myelomeningocele: A systematic review and meta-analysis.


Journal

Prenatal diagnosis
ISSN: 1097-0223
Titre abrégé: Prenat Diagn
Pays: England
ID NLM: 8106540

Informations de publication

Date de publication:
02 2021
Historique:
received: 15 09 2020
revised: 16 11 2020
accepted: 15 12 2020
pubmed: 12 1 2021
medline: 15 12 2021
entrez: 11 1 2021
Statut: ppublish

Résumé

We performed a systematic review to summarize the efficacy and safety of in utero stem cells application in preclinical models with myelomeningocele (MMC). The study was registered with PROSPERO (CRD42019160399). We searched MEDLINE, Embase, Web of Science, Scopus and CENTRAL for publications articles on stem cell therapy in animal fetuses with MMC until May 2020. Publication quality was assessed by the SYRCLE's tool. Meta-analyses were pooled if studies were done in the same animal model providing similar type of stem cell used and outcome measurements. Narrative synthesis was performed for studies that could not be pooled. Nineteen and seven studies were included in narrative and quantitative syntheses, respectively. Most used mesenchymal stem cells (MSCs) and primarily involved ovine and rodent models. Both intra-amniotic injection of allogeneic amniotic fluid (AF)-MSCs in rat MMC model and the application of human placental (P)-MSCs to the spinal cord during fetal surgery in MMC ovine model did not compromise fetal survival rates at term (rat model, relative risk [RR] 1.03, 95% CI 0.92-1.16; ovine model, RR 0.94, 95% CI 0.78-1.13). A single intra-amniotic injection of allogeneic AF-MSCs into rat MMC model was associated with a higher rate of complete defect coverage compared to saline injection (RR 16.35, 95% CI 3.27-81.79). The incorporation of human P-MSCs as a therapeutic adjunct to fetal surgery in the ovine MMC model significantly improved sheep locomotor rating scale after birth (mean difference 5.18, 95% CI 3.36-6.99). Stem cell application during prenatal period in preclinical animal models is safe and effective.

Identifiants

pubmed: 33427329
doi: 10.1002/pd.5887
pmc: PMC7611444
mid: EMS131082
doi:

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

283-300

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 101957
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT101957
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. Prenatal Diagnosis published by John Wiley & Sons Ltd.

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Auteurs

Yada Kunpalin (Y)

Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, UK.
Department of Development and Regeneration, Cluster Woman and Child, Biomedical Sciences, KU Leuven, Leuven, Belgium.

Sindhu Subramaniam (S)

Great Ormond Street Institute of Child Health, University College London, London, UK.

Silvia Perin (S)

Great Ormond Street Institute of Child Health, University College London, London, UK.

Mattia F M Gerli (MFM)

Great Ormond Street Institute of Child Health, University College London, London, UK.
Division of Surgery and Interventional Science, Royal Free Hospital, University College London, London, UK.

Jan Bosteels (J)

Department of Development and Regeneration, Cluster Woman and Child, Biomedical Sciences, KU Leuven, Leuven, Belgium.
Cochrane Belgium, Belgian Centre for Evidence-Based Medicine (Cebam), Leuven, Belgium.

Sebastien Ourselin (S)

School of Biomedical Engineering & Imaging Sciences, King's College London, London, UK.

Jan Deprest (J)

Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, UK.
Department of Development and Regeneration, Cluster Woman and Child, Biomedical Sciences, KU Leuven, Leuven, Belgium.
Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.

Paolo De Coppi (P)

Department of Development and Regeneration, Cluster Woman and Child, Biomedical Sciences, KU Leuven, Leuven, Belgium.
Great Ormond Street Institute of Child Health, University College London, London, UK.

Anna L David (AL)

Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, UK.
Department of Development and Regeneration, Cluster Woman and Child, Biomedical Sciences, KU Leuven, Leuven, Belgium.

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Classifications MeSH