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A Review of Placenta and Umbilical Cord-Derived Stem Cells and the Immunomodulatory Basis of Their Therapeutic Potential in Bronchopulmonary Dysplasia

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FRONTIERS IN PEDIATRICS
卷 9, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fped.2021.615508

关键词

bronchopulmonary dysplasia; placenta; regenerative medicine; stem cell; umbilical cord

资金

  1. Ministry of Higher Education of Malaysia through the Fundamental Research Grant Scheme [FRGS/1/2016/SKK08/UKM/03/5]

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Bronchopulmonary dysplasia (BPD) is a devastating lung disorder in preterm infants caused by abnormal reparative response, and current treatment strategies have limited success. Stem cell therapy, particularly using placenta-derived and umbilical cord-derived stem cells, shows potential in mitigating BPD, but further research and clinical trials are needed to confirm its effectiveness.
Bronchopulmonary dysplasia (BPD) is a devastating lung disorder of preterm infants as a result of an aberrant reparative response following exposures to various antenatal and postnatal insults. Despite sophisticated medical treatment in this modern era, the incidence of BPD remains unabated. The current strategies to prevent and treat BPD have met with limited success. The emergence of stem cell therapy may be a potential breakthrough in mitigating this complex chronic lung disorder. Over the last two decades, the human placenta and umbilical cord have gained increasing attention as a highly potential source of stem cells. Placenta-derived stem cells (PDSCs) and umbilical cord-derived stem cells (UCDSCs) display several advantages such as immune tolerance and are generally devoid of ethical constraints, in addition to their stemness qualities. They possess the characteristics of both embryonic and mesenchymal stromal/stem cells. Recently, there are many preclinical studies investigating the use of these cells as therapeutic agents in neonatal disease models for clinical applications. In this review, we describe the preclinical and clinical studies using PDSCs and UCDSCs as treatment in animal models of BPD. The source of these stem cells, routes of administration, and effects on immunomodulation, inflammation and regeneration in the injured lung are also discussed. Lastly, a brief description summarized the completed and ongoing clinical trials using PDSCs and UCDSCs as therapeutic agents in preventing or treating BPD. Due to the complexity of BPD, the development of a safe and efficient therapeutic agent remains a major challenge to both clinicians and researchers.

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