Division of Neonatology, Department of Pediatrics, Children's Mercy Kansas City, Kansas City, MO, USA.
Department of Cardiovascular Medicine, Cardiovascular Research Institute, University of Kansas Medical Center, Kansas City, MO, USA.
Pediatr Res. 2020 Jan;87(2):265-276. doi: 10.1038/s41390-019-0425-5. Epub 2019 May 14.
Diseases of the preterm newborn such as bronchopulmonary dysplasia, necrotizing enterocolitis, cerebral palsy, and hypoxic-ischemic encephalopathy continue to be major causes of infant mortality and long-term morbidity. Effective therapies for the prevention or treatment for these conditions are still lacking as recent clinical trials have shown modest or no benefit. Stem cell therapy is rapidly emerging as a novel therapeutic tool for several neonatal diseases with encouraging pre-clinical results that hold promise for clinical translation. However, there are a number of unanswered questions and facets to the development of stem cell therapy as a clinical intervention. There is much work to be done to fully elucidate the mechanisms by which stem cell therapy is effective (e.g., anti-inflammatory versus pro-angiogenic), identifying important paracrine mediators, and determining the timing and type of therapy (e.g., cellular versus secretomes), as well as patient characteristics that are ideal. Importantly, the interaction between stem cell therapy and current, standard-of-care interventions is nearly completely unknown. In this review, we will focus predominantly on the use of mesenchymal stromal cells for neonatal diseases, highlighting the promises and challenges in clinical translation towards preventing neonatal diseases in the 21st century.
早产儿疾病,如支气管肺发育不良、坏死性小肠结肠炎、脑瘫和缺氧缺血性脑病,仍然是婴儿死亡和长期发病的主要原因。由于最近的临床试验显示效果有限或没有效果,因此仍然缺乏针对这些疾病的有效预防或治疗方法。干细胞治疗作为一种新的治疗工具,正在迅速成为几种新生儿疾病的治疗方法,其令人鼓舞的临床前结果为临床转化提供了希望。然而,作为一种临床干预措施,干细胞治疗的发展还存在许多悬而未决的问题和方面。为了充分阐明干细胞治疗的作用机制(例如抗炎与促血管生成),确定重要的旁分泌介质,以及确定治疗的时间和类型(例如细胞与分泌组),以及确定理想的患者特征,还有很多工作要做。重要的是,干细胞治疗与当前标准治疗干预措施之间的相互作用几乎完全未知。在这篇综述中,我们将主要关注间充质基质细胞在新生儿疾病中的应用,突出强调在 21 世纪预防新生儿疾病的临床转化方面的前景和挑战。