Félix Joana, Matias Alexandra, Bartosch Carla
Department of Obstetrics and Gynecology, Hospital Pedro Hispano, Rua Dr. Eduardo Torres, 4464-513, Senhora da Hora, Portugal.
Department of Obstetrics and Gynecology, Hospital São João, Alameda Professor Hernâni Monteiro, 4200-319, Porto, Portugal.
Arch Gynecol Obstet. 2025 Jun;311(6):1553-1560. doi: 10.1007/s00404-024-07902-7. Epub 2025 Jan 20.
Preterm birth remains a global health challenge with significant perinatal morbidity and mortality rates. Despite extensive research, the underlying mechanisms triggering preterm birth remain elusive, needing a deeper understanding of cervical cellular remodelling processes.
This study aims to elucidate the cellular mechanisms underlying cervical remodelling in spontaneous preterm labour (PTL) compared to term labour (TL), focusing on the roles of inflammatory cells and fibroblasts.
We conducted a prospective observational study from October 2018 to March 2021, at two hospitals. Participants were categorized into two groups: PTL (n = 14), TL (n = 14). A small set (n = 6) of preterm not in labour (PTnotL) was also included. Cervical biopsies were obtained and analysed for the density of fibroblasts and inflammatory cells (neutrophils and mononuclear cells) using digital image analysis. Statistical analysis was performed employing Mann-Whitney and Kruskal-Wallis tests.
There was no significant overall difference in global inflammatory cell density between PTL and TL (p = 0.154). However, a detailed analysis revealed significantly higher inflammation in the exocervix of PTL compared to TL, particularly involving neutrophils (p = 0.021) and mononuclear cells (p = 0.028). Neutrophils (p = 0.035), but not mononuclear cells (p = 0.111), were significantly decreased in PTnotL exocervix compared to PTL. No differences were found in inflammatory cell density in the endocervix. Fibroblast densities were similar across groups.
This study highlights the distinct cellular profiles in the cervix during preterm and term labour, with neutrophils playing a pivotal role in preterm labour. These findings may guide the development of targeted interventions to prevent preterm birth.
早产仍然是一项全球性的健康挑战,围产期发病率和死亡率很高。尽管进行了广泛的研究,但引发早产的潜在机制仍然难以捉摸,需要更深入地了解宫颈细胞重塑过程。
本研究旨在阐明与足月分娩(TL)相比,自发性早产(PTL)时宫颈重塑的细胞机制,重点关注炎症细胞和成纤维细胞的作用。
我们于2018年10月至2021年3月在两家医院进行了一项前瞻性观察研究。参与者分为两组:PTL组(n = 14),TL组(n = 14)。还纳入了一小部分(n = 6)未临产的早产(PTnotL)患者。获取宫颈活检组织,并使用数字图像分析来分析成纤维细胞和炎症细胞(中性粒细胞和单核细胞)的密度。采用Mann-Whitney检验和Kruskal-Wallis检验进行统计分析。
PTL组和TL组之间总体炎症细胞密度无显著差异(p = 0.154)。然而,详细分析显示,与TL组相比,PTL组宫颈外口的炎症明显更严重,尤其是涉及中性粒细胞(p = 0.021)和单核细胞(p = 0.028)。与PTL组相比,PTnotL组宫颈外口中性粒细胞显著减少(p = 0.035),但单核细胞无显著减少(p = 0.111)。宫颈内口的炎症细胞密度无差异。各组间成纤维细胞密度相似。
本研究突出了早产和足月分娩时宫颈不同的细胞特征,中性粒细胞在早产中起关键作用。这些发现可能会指导预防早产的靶向干预措施的开发。