Plasma proteomic signature of neonates in the context of placental histological chorioamnionitis.

IF 2 4区 医学 Q2 PEDIATRICS BMJ Paediatrics Open Pub Date : 2024-09-04 DOI:10.1136/bmjpo-2024-002708
Jing Liu, Die Liu, Qi Sun, Yunchao Su, Lijuan Tang, Haixiao Liang, Fang Ye, Yuanmei Chen, Qi Zhang
{"title":"Plasma proteomic signature of neonates in the context of placental histological chorioamnionitis.","authors":"Jing Liu, Die Liu, Qi Sun, Yunchao Su, Lijuan Tang, Haixiao Liang, Fang Ye, Yuanmei Chen, Qi Zhang","doi":"10.1136/bmjpo-2024-002708","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":9069,"journal":{"name":"BMJ Paediatrics Open","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11381644/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMJ Paediatrics Open","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1136/bmjpo-2024-002708","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
胎盘组织学绒毛膜羊膜炎背景下的新生儿血浆蛋白质组特征。
背景:胎盘组织学绒毛膜羊膜炎(HCA)被认为是导致新生儿各种不良结局的重要风险因素。本研究旨在探讨新生儿的炎症蛋白水平是否与 HCA 相关:方法:选取 2020 年 2 月至 2022 年 11 月期间的所有单胎产妇,根据母体胎盘病理学结果分为三组:HCA 1 期组(24 人)、HCA 2 期组(16 人)和对照组(17 人)。Olink Target 96 炎症面板用于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。我们通过差异蛋白表达分析比较了蛋白谱:结果:共有 6 种炎症相关蛋白在 HCA 1 期组和对照组之间存在显著差异。具体来说,TRANCE和CST5的表达明显上调(分别为p=0.006和p=0.025),而IFN-gamma、CXCL9、CXCL10和CCL19的表达则明显下调(分别为p=0.040、p=0.046、p=0.007和p=0.006)。与对照组相比,HCA 2 期新生儿的 CD5 和 CD6 水平明显升高,IFN-gamma、CXCL10 和 CCL19 水平下降。这些差异蛋白在细胞因子活性正向调节、白细胞趋化和T细胞活化途径正向调节相关的基因本体术语中明显富集。京都基因和基因组百科全书》的通路分析表明,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-kappa B/toll样受体/凝血因子信号通路以及细胞因子与细胞因子受体的相互作用存在明显差异。斯皮尔曼分析表明,不仅在新生儿白细胞中,而且在母体白细胞中,CD6 和 CD5 蛋白水平之间都存在明显的正相关。此外,还发现 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 蛋白可能是 HCA 相关新生儿疾病的潜在致病因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
BMJ Paediatrics Open
BMJ Paediatrics Open Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.10
自引率
3.80%
发文量
124
期刊最新文献
Effectiveness and feasibility of continuous renal replacement therapy for acute kidney injury in neonates weighing 3 kg or less: a two-centre, retrospective study. Power to change: a 21st-century paediatrician and their patient in conversation. Effects of a hospital-based food security programme for children with complex diseases in an upper-middle-income country: a before-and-after study. Tanner's target height formula underestimates final adult height in Korean adolescents and young adults: reassessment of target height based on the Korean National Health and Nutrition Examination Survey 2010-2019. Use of intranasal and sublingual analgesia in children and adolescents in the paediatric emergency department.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1