子痫前期外周调节性B细胞程序性细胞死亡蛋白1的表达减少-免疫抑制受损的迹象

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Sophie Brondt Salby , Gry Persson , Nanna Heldager Pedersen , Gökmen Turan , Laura Kimmerslev , Katrine Folmann Finne , Iben Weisdorf , Morten Lebech , Thomas Vauvert F. Hviid
{"title":"子痫前期外周调节性B细胞程序性细胞死亡蛋白1的表达减少-免疫抑制受损的迹象","authors":"Sophie Brondt Salby ,&nbsp;Gry Persson ,&nbsp;Nanna Heldager Pedersen ,&nbsp;Gökmen Turan ,&nbsp;Laura Kimmerslev ,&nbsp;Katrine Folmann Finne ,&nbsp;Iben Weisdorf ,&nbsp;Morten Lebech ,&nbsp;Thomas Vauvert F. Hviid","doi":"10.1016/j.jri.2025.104426","DOIUrl":null,"url":null,"abstract":"<div><div>Immunological changes are believed to be a part of pre-eclampsia etiology. This study investigated the distribution of the specific peripheral B lymphocyte phenotypes in pre-eclampsia cases compared to uncomplicated pregnancies. The study cohort included 29 women with pre-eclampsia and 14 women with uncomplicated pregnancies. Blood samples were collected in the third trimester of primigravidae pregnancies, and immune cells were analyzed using flow cytometry. Cases with pre-eclampsia showed a significantly reduced expression of programmed cell death protein 1 (PD-1) on CD27<sup>+</sup>CD24<sup>hi</sup>CD38<sup>hi</sup> regulatory B cells compared with control pregnancies (p = 0.002; multivariate logistic regression: p = 0.009). Trends for a reduced PD-1 expression on regulatory CD27<sup>+</sup>CD24<sup>hi</sup> B cells and on live CD19<sup>+</sup> B cells were observed in cases of pre-eclampsia (p = 0.011 and p = 0.035; respectively). No significant differences between pre-eclampsia cases and controls in percentages of B cells, B1a cells, plasmablasts, naïve B cells, transitional/immature B cells, memory B cells, regulatory CD27<sup>+</sup>CD24<sup>hi</sup> B cells and regulatory CD27<sup>+</sup>CD24<sup>hi</sup>CD38<sup>hi</sup> B cells were observed. This is the first study to report reduced PD-1 expression on live B cells and regulatory B cells in pre-eclampsia. These results are in line with previous studies of peripheral regulatory T cells and decidual lymphocytes from pre-eclampsia patients. Reduced PD-1 expression on regulatory B cells in pre-eclampsia could indicate that a lack of immune suppression might play a role in the pathophysiology of pre-eclampsia.</div></div>","PeriodicalId":16963,"journal":{"name":"Journal of Reproductive Immunology","volume":"168 ","pages":"Article 104426"},"PeriodicalIF":2.9000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reduced expression of programmed cell death protein 1 on peripheral regulatory B cells in pre-eclampsia – Signs of impaired immune suppression\",\"authors\":\"Sophie Brondt Salby ,&nbsp;Gry Persson ,&nbsp;Nanna Heldager Pedersen ,&nbsp;Gökmen Turan ,&nbsp;Laura Kimmerslev ,&nbsp;Katrine Folmann Finne ,&nbsp;Iben Weisdorf ,&nbsp;Morten Lebech ,&nbsp;Thomas Vauvert F. Hviid\",\"doi\":\"10.1016/j.jri.2025.104426\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Immunological changes are believed to be a part of pre-eclampsia etiology. This study investigated the distribution of the specific peripheral B lymphocyte phenotypes in pre-eclampsia cases compared to uncomplicated pregnancies. The study cohort included 29 women with pre-eclampsia and 14 women with uncomplicated pregnancies. Blood samples were collected in the third trimester of primigravidae pregnancies, and immune cells were analyzed using flow cytometry. Cases with pre-eclampsia showed a significantly reduced expression of programmed cell death protein 1 (PD-1) on CD27<sup>+</sup>CD24<sup>hi</sup>CD38<sup>hi</sup> regulatory B cells compared with control pregnancies (p = 0.002; multivariate logistic regression: p = 0.009). Trends for a reduced PD-1 expression on regulatory CD27<sup>+</sup>CD24<sup>hi</sup> B cells and on live CD19<sup>+</sup> B cells were observed in cases of pre-eclampsia (p = 0.011 and p = 0.035; respectively). No significant differences between pre-eclampsia cases and controls in percentages of B cells, B1a cells, plasmablasts, naïve B cells, transitional/immature B cells, memory B cells, regulatory CD27<sup>+</sup>CD24<sup>hi</sup> B cells and regulatory CD27<sup>+</sup>CD24<sup>hi</sup>CD38<sup>hi</sup> B cells were observed. This is the first study to report reduced PD-1 expression on live B cells and regulatory B cells in pre-eclampsia. These results are in line with previous studies of peripheral regulatory T cells and decidual lymphocytes from pre-eclampsia patients. Reduced PD-1 expression on regulatory B cells in pre-eclampsia could indicate that a lack of immune suppression might play a role in the pathophysiology of pre-eclampsia.</div></div>\",\"PeriodicalId\":16963,\"journal\":{\"name\":\"Journal of Reproductive Immunology\",\"volume\":\"168 \",\"pages\":\"Article 104426\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Reproductive Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S016503782500004X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Reproductive Immunology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S016503782500004X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

免疫变化被认为是子痫前期病因的一部分。本研究探讨了子痫前期病例与未并发症妊娠的特异性外周B淋巴细胞表型的分布。研究队列包括29名先兆子痫妇女和14名无并发症妊娠妇女。在初生蜂科妊娠晚期采集血样,用流式细胞术分析免疫细胞。与对照组妊娠相比,子痫前期患者CD27+CD24hiCD38hi调节性B细胞上程序性细胞死亡蛋白1 (PD-1)的表达显著降低(p = 0.002;多因素logistic回归:p = 0.009)。在子痫前期患者中,PD-1在调节性CD27+CD24hi B细胞和活CD19+ B细胞上的表达降低(p = 0.011和p = 0.035;分别)。子痫前期患者B细胞、B1a细胞、浆母细胞、naïve B细胞、过渡/未成熟B细胞、记忆B细胞、调节性CD27+CD24hi B细胞和调节性CD27+CD24hiCD38hi B细胞的百分比与对照组无显著差异。这是首次报道子痫前期活B细胞和调节性B细胞中PD-1表达降低的研究。这些结果与先前对子痫前期患者外周血调节性T细胞和蜕膜淋巴细胞的研究一致。子痫前期调节性B细胞PD-1表达降低可能提示免疫抑制缺失可能在子痫前期病理生理中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced expression of programmed cell death protein 1 on peripheral regulatory B cells in pre-eclampsia – Signs of impaired immune suppression
Immunological changes are believed to be a part of pre-eclampsia etiology. This study investigated the distribution of the specific peripheral B lymphocyte phenotypes in pre-eclampsia cases compared to uncomplicated pregnancies. The study cohort included 29 women with pre-eclampsia and 14 women with uncomplicated pregnancies. Blood samples were collected in the third trimester of primigravidae pregnancies, and immune cells were analyzed using flow cytometry. Cases with pre-eclampsia showed a significantly reduced expression of programmed cell death protein 1 (PD-1) on CD27+CD24hiCD38hi regulatory B cells compared with control pregnancies (p = 0.002; multivariate logistic regression: p = 0.009). Trends for a reduced PD-1 expression on regulatory CD27+CD24hi B cells and on live CD19+ B cells were observed in cases of pre-eclampsia (p = 0.011 and p = 0.035; respectively). No significant differences between pre-eclampsia cases and controls in percentages of B cells, B1a cells, plasmablasts, naïve B cells, transitional/immature B cells, memory B cells, regulatory CD27+CD24hi B cells and regulatory CD27+CD24hiCD38hi B cells were observed. This is the first study to report reduced PD-1 expression on live B cells and regulatory B cells in pre-eclampsia. These results are in line with previous studies of peripheral regulatory T cells and decidual lymphocytes from pre-eclampsia patients. Reduced PD-1 expression on regulatory B cells in pre-eclampsia could indicate that a lack of immune suppression might play a role in the pathophysiology of pre-eclampsia.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.30
自引率
5.90%
发文量
162
审稿时长
10.6 weeks
期刊介绍: Affiliated with the European Society of Reproductive Immunology and with the International Society for Immunology of Reproduction The aim of the Journal of Reproductive Immunology is to provide the critical forum for the dissemination of results from high quality research in all aspects of experimental, animal and clinical reproductive immunobiology. This encompasses normal and pathological processes of: * Male and Female Reproductive Tracts * Gametogenesis and Embryogenesis * Implantation and Placental Development * Gestation and Parturition * Mammary Gland and Lactation.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信