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间充质基质细胞在支气管肺发育不良治疗中的作用:针对一种异质性疾病的多管齐下方法

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

作者信息

Deguise Marc-Olivier, Thébaud Bernard

机构信息

Division of Neonatology, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.

出版信息

Compr Physiol. 2025 Aug;15(4):e70038. doi: 10.1002/cph4.70038.


DOI:10.1002/cph4.70038
PMID:40853849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12377523/
Abstract

Acute lung injury can be a devastating ailment leading to death in patients of all ages. In preterm neonates, lung injury is unique and unlike what is seen in pediatric and adult populations. The physiology behind the acute lung injury endured in developing lungs and the chronicity of harmful stimuli vastly distinguish how bronchopulmonary dysplasia (BPD), the most common complication of prematurity, settles in as a chronic lung disease with lifetime sequelae. Despite being recognized for over 50 years, BPD continues to puzzle the world of neonatology with a shifting phenotype that parallels improvement in neonatal care. The improved understanding of BPD's far-reaching and long-term consequences on the lung and other organs highlights the need to find effective interventions, making it a priority of neonatal research. In this review, we provide an overview of BPD and its associated consequences. Then, we examine the biological premises for mesenchymal stromal cells as a promising therapy, reviewing current translational efforts, challenges, and future directions toward bringing mesenchymal stromal cell therapy to BPD patients.

摘要

急性肺损伤可能是一种毁灭性疾病,可导致各年龄段患者死亡。在早产新生儿中,肺损伤具有独特性,与儿科和成人人群中所见不同。发育中的肺所遭受的急性肺损伤背后的生理学以及有害刺激的慢性程度,极大地区分了支气管肺发育不良(BPD)这一最常见的早产并发症如何发展为一种具有终生后遗症的慢性肺病。尽管BPD已被认识超过50年,但它不断变化的表型与新生儿护理的改善并行,仍然困扰着新生儿学界。对BPD对肺和其他器官的深远和长期后果的更好理解凸显了寻找有效干预措施的必要性,使其成为新生儿研究的一个优先事项。在本综述中,我们概述了BPD及其相关后果。然后,我们研究间充质基质细胞作为一种有前景的治疗方法的生物学前提,回顾当前的转化研究工作、挑战以及将间充质基质细胞疗法应用于BPD患者的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/bc1f03a5665b/CPH4-15-e70038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/6850a3704776/CPH4-15-e70038-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/bb7680c4964c/CPH4-15-e70038-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/ffec89886d14/CPH4-15-e70038-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/bc1f03a5665b/CPH4-15-e70038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/6850a3704776/CPH4-15-e70038-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/bb7680c4964c/CPH4-15-e70038-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/ffec89886d14/CPH4-15-e70038-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6f/12377523/bc1f03a5665b/CPH4-15-e70038-g001.jpg

相似文献

[1]
The Role of Mesenchymal Stromal Cells in the Treatment of Bronchopulmonary Dysplasia: A Multi-Prong Approach for a Heterogeneous Disease.

Compr Physiol. 2025-8

[2]
Prescription of Controlled Substances: Benefits and Risks

2025-1

[3]
Systemic corticosteroid regimens for prevention of bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2023-3-13

[4]
Early (< 8 days) systemic postnatal corticosteroids for prevention of bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2017-10-24

[5]
Delivery room interventions to prevent bronchopulmonary dysplasia in preterm infants: a protocol for a systematic review and network meta-analysis.

BMJ Open. 2019-8-18

[6]
Systemic corticosteroid regimens for prevention of bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2017-1-31

[7]
Superoxide dismutase for bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2023-10-9

[8]
Late (> 7 days) systemic postnatal corticosteroids for prevention of bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2017-10-24

[9]
Early (&lt; 7 days) systemic postnatal corticosteroids for prevention of bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2021-10-21

[10]
Late (≥ 7 days) inhalation corticosteroids to reduce bronchopulmonary dysplasia in preterm infants.

Cochrane Database Syst Rev. 2017-8-24

本文引用的文献

[1]
Advancing mesenchymal stromal cell therapy: The crucial role of updated guidelines.

Cytotherapy. 2025-5

[2]
Cell-based therapies in preclinical models of necrotizing enterocolitis: a systematic review and meta-analysis.

Stem Cells Transl Med. 2025-2-11

[3]
Neonatal intermittent hypoxemia events are associated with later systemic hypertension.

Pediatr Res. 2025-1-31

[4]
Respiratory distress syndrome is the poster child for neonatology.

Pediatr Res. 2025-1-16

[5]
Updates on neonatal cell and novel therapeutics: Proceedings of the Second Neonatal Cell Therapies Symposium (2024).

Pediatr Res. 2025-1-15

[6]
AI models in clinical neonatology: a review of modeling approaches and a consensus proposal for standardized reporting of model performance.

Pediatr Res. 2024-12-17

[7]
Delphi-driven consensus definition for mesenchymal stromal cells and clinical reporting guidelines for mesenchymal stromal cell-based therapeutics.

Cytotherapy. 2025-2

[8]
Systemic Postnatal Corticosteroids, Bronchopulmonary Dysplasia, and Survival Free of Cerebral Palsy.

JAMA Pediatr. 2025-1-1

[9]
Eligible Infants Included in Neonatal Clinical Trials and Reasons for Noninclusion: A Systematic Review.

JAMA Netw Open. 2024-10-1

[10]
The emerging roles of microbiome and short-chain fatty acids in the pathogenesis of bronchopulmonary dysplasia.

Front Cell Infect Microbiol. 2024

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