Department of Pediatrics, China-Japan Friendship Hospital, Beijing, China.
Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
BMJ Paediatr Open. 2024 Sep 4;8(1):e002708. doi: 10.1136/bmjpo-2024-002708.
Placental histological chorioamnionitis (HCA) is recognised as a significant risk factor for various adverse neonatal outcomes. This study aims to explore if the inflammatory protein levels in neonates were associated with HCA.
All women with singleton births from February 2020 to November 2022 were selected and divided into three groups based on maternal placental pathology results: the HCA-stage 1 group (n=24), the HCA-stage 2 group (n=16) and the control group (n=17). Olink Target 96 Inflammation Panel was used to detect the levels of 92 inflammation-related proteins in the plasma of newborns from all three groups within 24 hours after birth. We compared the protein profiles through differential protein expression analysis.
A total of six inflammation-related proteins exhibited significant differences between the HCA-stage 1 and the control group. Specifically, TRANCE and CST5 were significantly upregulated (p=0.006, p=0.025, respectively), whereas the expression of IFN-gamma, CXCL9, CXCL10 and CCL19 was significantly downregulated (p=0.040, p=0.046, p=0.007, p=0.006, respectively). HCA-stage 2 newborns had significantly elevated levels of CD5 and CD6 and decreased IFN-gamma, CXCL10 and CCL19 in comparison to controls. These differential proteins were significantly enriched in positive regulation of cytokine activity, leucocyte chemotaxis and positive regulation of T-cell activation pathway-related Gene Ontology terms. Kyoto Encyclopedia of Genes and Genomes pathway analysis revealed that viral protein interaction with cytokine and cytokine receptor, interleukin-17/NF-kappa B/toll-like receptor/chemokine signalling pathway, and cytokine-cytokine receptor interaction exhibited significant differences. Spearman analysis demonstrated a significant positive connection between the levels of CD6 and CD5 proteins, not only in neonatal leucocytes but also in maternal leucocytes. Additionally, CD6 was found to be associated with neonatal birth weight.
In conclusion, placental histological changes associated with chorioamnionitis appear to influence the expression of inflammatory proteins in offspring. Notably, CD6 and CD5 proteins may potentially contribute to the pathogenesis of HCA-related neonatal diseases.
胎盘组织学绒毛膜羊膜炎(HCA)被认为是各种不良新生儿结局的重要危险因素。本研究旨在探讨新生儿的炎症蛋白水平是否与 HCA 有关。
选择 2020 年 2 月至 2022 年 11 月期间所有单胎分娩的妇女,并根据产妇胎盘病理结果将其分为三组:HCA 1 期组(n=24)、HCA 2 期组(n=16)和对照组(n=17)。使用 Olink Target 96 炎症面板检测三组新生儿出生后 24 小时内血浆中 92 种炎症相关蛋白的水平。通过差异蛋白表达分析比较蛋白图谱。
HCA 1 期组与对照组之间共有 6 种炎症相关蛋白存在显著差异。具体而言,TRANCE 和 CST5 显著上调(p=0.006,p=0.025),而 IFN-γ、CXCL9、CXCL10 和 CCL19 的表达则显著下调(p=0.040,p=0.046,p=0.007,p=0.006)。与对照组相比,HCA 2 期新生儿的 CD5 和 CD6 水平显著升高,IFN-γ、CXCL10 和 CCL19 水平降低。这些差异蛋白在细胞因子活性的正调控、白细胞趋化和 T 细胞激活途径的正调控等基因本体术语中显著富集。京都基因与基因组百科全书通路分析显示,病毒蛋白与细胞因子和细胞因子受体的相互作用、白细胞介素-17/NF-κB/ Toll 样受体/趋化因子信号通路和细胞因子-细胞因子受体相互作用存在显著差异。Spearman 分析表明,新生儿白细胞和产妇白细胞中 CD6 和 CD5 蛋白水平之间存在显著正相关。此外,CD6 与新生儿出生体重有关。
总之,与绒毛膜羊膜炎相关的胎盘组织学变化似乎会影响后代炎症蛋白的表达。值得注意的是,CD6 和 CD5 蛋白可能与 HCA 相关新生儿疾病的发病机制有关。