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利用基于细胞的策略打破支气管肺发育不良与晚年慢性肺病发展之间的联系。

Using Cell-Based Strategies to Break the Link between Bronchopulmonary Dysplasia and the Development of Chronic Lung Disease in Later Life.

作者信息

O'Reilly Megan, Thébaud Bernard

机构信息

Department of Pediatrics, Women and Children's Health Research Institute, Katz Group Centre for Pharmacy and Health Research, University of Alberta, Edmonton, AB, Canada T6G 2E1.

出版信息

Pulm Med. 2013;2013:874161. doi: 10.1155/2013/874161. Epub 2013 Jan 14.

Abstract

Bronchopulmonary dysplasia (BPD) is the chronic lung disease of prematurity that affects very preterm infants. Although advances in perinatal care have changed the course of lung injury and enabled the survival of infants born as early as 23-24 weeks of gestation, BPD still remains a common complication of extreme prematurity, and there is no specific treatment for it. Furthermore, children, adolescents, and adults who were born very preterm and developed BPD have an increased risk of persistent lung dysfunction, including early-onset emphysema. Therefore, it is possible that early-life pulmonary insults, such as extreme prematurity and BPD, may increase the risk of COPD later in life, especially if exposed to secondary challenges such as respiratory infections and/or smoking. Recent advances in our understanding of stem/progenitor cells and their potential to repair damaged organs offer the possibility of cell-based treatments for neonatal and adult lung injuries. This paper summarizes the long-term pulmonary outcomes of preterm birth and BPD and discusses the recent advances of cell-based therapies for lung diseases, with a particular focus on BPD and COPD.

摘要

支气管肺发育不良(BPD)是一种影响极早产儿的慢性肺部疾病。尽管围产期护理的进步改变了肺损伤的病程,并使妊娠23 - 24周出生的婴儿得以存活,但BPD仍然是极早产常见的并发症,且尚无针对其的特效治疗方法。此外,极早产并患BPD的儿童、青少年及成人出现持续性肺功能障碍的风险增加,包括早发性肺气肿。因此,诸如极早产和BPD等生命早期的肺部损伤可能会增加日后患慢性阻塞性肺疾病(COPD)的风险,尤其是在接触诸如呼吸道感染和/或吸烟等二次挑战时。我们对干细胞/祖细胞及其修复受损器官潜力的最新认识进展为新生儿和成人肺部损伤的细胞治疗提供了可能。本文总结了早产和BPD的长期肺部转归,并讨论了肺部疾病细胞治疗的最新进展,尤其关注BPD和COPD。

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