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Mesenchymal stem cells for the prevention and treatment of bronchopulmonary dysplasia in preterm infants.

作者信息

Pierro Maria, Thébaud Bernard, Soll Roger

机构信息

Department of Clinical Sciences and Community Health, University of Milan, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.

出版信息

Cochrane Database Syst Rev. 2017 Nov 10;11(11):CD011932. doi: 10.1002/14651858.CD011932.pub2.


DOI:10.1002/14651858.CD011932.pub2
PMID:29125893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6485972/
Abstract

BACKGROUND: Bronchopulmonary dysplasia (BPD) remains a major complication of prematurity and currently lacks efficient treatments. Mesenchymal stem/stromal cells (MSCs) have been extensively explored as a potential therapy in several preclinical and clinical settings. Human and animal MSCs have been shown to prevent and treat lung injury in various preclinical models of lung diseases, including experimental BPD. OBJECTIVES: To determine if MSCs, administered intravenously or endotracheally, are safe and effective in preventing or treating BPD, or both, in preterm infants. SEARCH METHODS: We used the standard search strategy of the Cochrane Neonatal Review Group to search the Cochrane Central Register of Controlled Trials (CENTRAL 2016, Issue 10), MEDLINE via PubMed (1966 to 6 November 2016), Embase (1980 to 6 November 2016), and CINAHL (1982 to 6 November 2016). We also searched clinical trials databases, conference proceedings, and the reference lists of retrieved articles for randomized controlled trials (RCTs) and quasi-RCTs. SELECTION CRITERIA: We considered RCTs and quasi-RCTs investigating prevention or treatment of BPD, or both, in preterm infants. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed trial quality according to prespecified criteria. MAIN RESULTS: We found no RCTs or quasi-RCTs addressing the use of MSCs for prevention or treatment of BPD in premature infants. Two RCTs are currently registered and ongoing. AUTHORS' CONCLUSIONS: There is insufficient evidence to determine the safety and efficacy of MSCs in the treatment or prevention of BPD in premature infants. The results of the ongoing trials addressing this issue are expected in the near future.

摘要

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引用本文的文献

[1]
Mesenchymal Stromal Cell Therapy Restores Intestinal Integrity and Attentuates Inflammation in a Preterm Piglet Model of Necrotizing Enterocolitis.

Res Sq. 2025-8-18

[2]
The Role of Mesenchymal Stromal Cells in the Treatment of Bronchopulmonary Dysplasia: A Multi-Prong Approach for a Heterogeneous Disease.

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[3]
Strategies for the prevention of bronchopulmonary dysplasia.

Front Pediatr. 2024-7-24

[4]
Strategies for cessation of caffeine administration in preterm infants.

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[5]
Stem cell-based interventions for the treatment of stroke in newborn infants.

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[6]
Stem cell-based interventions for the prevention and treatment of intraventricular haemorrhage and encephalopathy of prematurity in preterm infants.

Cochrane Database Syst Rev. 2023-2-15

[7]
Prophylactic Administration of Mesenchymal Stromal Cells Does Not Prevent Arrested Lung Development in Extremely Premature-Born Non-Human Primates.

Stem Cells Transl Med. 2023-3-3

[8]
Safety and Efficacy of Mesenchymal Stem Cells for the Treatment of Evolving and Established Bronchopulmonary Dysplasia: A Systematic Literature Review.

Cureus. 2022-12-16

[9]
Autologous cord blood mononuclear cell infusion for the prevention of bronchopulmonary dysplasia in very preterm monozygotic twins: A study protocol for a randomized, placebo-controlled, double-blinded multicenter trial.

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[10]
Intratracheal administration of umbilical cord-derived mesenchymal stem cells attenuates hyperoxia-induced multi-organ injury heme oxygenase-1 and JAK/STAT pathways.

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本文引用的文献

[1]
Serious adverse events of cell therapy for respiratory diseases: a systematic review and meta-analysis.

Oncotarget. 2017-5-2

[2]
Two-Year Follow-Up Outcomes of Premature Infants Enrolled in the Phase I Trial of Mesenchymal Stem Cells Transplantation for Bronchopulmonary Dysplasia.

J Pediatr. 2017-6

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N Engl J Med. 2017-3-16

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PLoS One. 2016-10-6

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Acute promyelocytic leukemia following autologous bone marrow-derived mesenchymal stem cell transplantation for traumatic brain injury: A case report.

Oncol Lett. 2015-11

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Taiwan J Obstet Gynecol. 2015-12

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Exp Clin Transplant. 2015-12

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Stem Cell Res Ther. 2015-11-23

[9]
Hospital variation and risk factors for bronchopulmonary dysplasia in a population-based cohort.

JAMA Pediatr. 2015-2-2

[10]
The challenge of defining mesenchymal stromal cell potency assays and their potential use as release criteria.

Cytotherapy. 2015-2

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