Boyle Ashley K, Tetorou Konstantina, Suff Natalie, Beecroft Laura, Mazzaschi Margherita, Karda Rajvinder, Hristova Mariya, Waddington Simon N, Peebles Donald
Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, United Kingdom.
Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, United Kingdom.
Am J Pathol. 2025 May;195(5):891-906. doi: 10.1016/j.ajpath.2025.01.008. Epub 2025 Jan 30.
Preterm birth (PTB; delivery before 37 weeks), the main cause of neonatal death worldwide, can lead to adverse neurodevelopmental outcomes, as well as lung and gut pathology. PTB can be associated with ascending vaginal infection. Ascending Escherichia coli infection in pregnant mice induces PTB and reduces pup survival. The current study demonstrated that this model recapitulates the pathology observed in human preterm neonates (namely, neuroinflammation, lung injury, and gut inflammation). In neonatal brains, there is widespread cell death, microglial activation, astrogliosis, and reduced neuronal density. The utility of this model was validated by assessing the efficacy of maternal cervical gene therapy with an adeno-associated viral vector containing human β defensin 3. This improved pup survival and reduced tumor necrosis factor alpha mRNA expression in perinatal pup brains exposed to E. coli. This model provides a unique opportunity to evaluate the therapeutic benefit of preterm labor interventions on perinatal pathology.
早产(PTB;妊娠37周前分娩)是全球新生儿死亡的主要原因,可导致不良的神经发育结局以及肺部和肠道病变。早产可能与上行性阴道感染有关。怀孕小鼠的上行性大肠杆菌感染会诱发早产并降低幼崽存活率。当前的研究表明,该模型概括了在人类早产新生儿中观察到的病理情况(即神经炎症、肺损伤和肠道炎症)。在新生儿大脑中,存在广泛的细胞死亡现象、小胶质细胞激活、星形胶质细胞增生以及神经元密度降低。通过评估使用携带人β-防御素3的腺相关病毒载体进行母体宫颈基因治疗的疗效,验证了该模型的实用性。这提高了幼崽存活率,并降低了暴露于大肠杆菌的围产期幼崽大脑中肿瘤坏死因子α mRNA的表达。该模型为评估早产干预措施对围产期病理的治疗益处提供了独特的机会。