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Hofbauer Cells: Their Role in Healthy and Complicated Pregnancy.成骨细胞:它们在健康和复杂妊娠中的作用。
Front Immunol. 2018 Nov 15;9:2628. doi: 10.3389/fimmu.2018.02628. eCollection 2018.
2
Fetal death: an extreme manifestation of maternal anti-fetal rejection.胎儿死亡:母体抗胎儿排斥反应的一种极端表现。
J Perinat Med. 2017 Oct 26;45(7):851-868. doi: 10.1515/jpm-2017-0073.
3
A novel in vitro model of villitis of unknown etiology demonstrates altered placental hormone and cytokine profile.一种未知病因绒毛膜炎的新型体外模型显示胎盘激素和细胞因子谱改变。
Am J Reprod Immunol. 2017 Nov;78(5). doi: 10.1111/aji.12725. Epub 2017 Jul 6.
4
Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement.胎盘病变的采样与定义:阿姆斯特丹胎盘研讨会小组共识声明
Arch Pathol Lab Med. 2016 Jul;140(7):698-713. doi: 10.5858/arpa.2015-0225-CC. Epub 2016 May 25.
5
Characterizing Villitis of Unknown Etiology and Inflammation in Stillbirth.不明病因绒毛炎及死产中的炎症特征分析
Am J Pathol. 2016 Apr;186(4):952-61. doi: 10.1016/j.ajpath.2015.12.010. Epub 2016 Feb 3.
6
Animal Models to Study Placental Development and Function throughout Normal and Dysfunctional Human Pregnancy.用于研究正常和异常人类妊娠期间胎盘发育及功能的动物模型
Semin Reprod Med. 2016 Jan;34(1):11-6. doi: 10.1055/s-0035-1570031. Epub 2016 Jan 11.
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Systematic review of placental pathology reported in association with stillbirth.与死产相关的胎盘病理学系统评价。
Placenta. 2014 Aug;35(8):552-62. doi: 10.1016/j.placenta.2014.05.011. Epub 2014 Jun 6.
8
Immunomodulatory effects of sex hormones: requirements for pregnancy and relevance in melanoma.性激素的免疫调节作用:妊娠的要求及在黑色素瘤中的相关性。
Mayo Clin Proc. 2014 Apr;89(4):520-35. doi: 10.1016/j.mayocp.2014.01.006.
9
Investigating the association of villitis of unknown etiology with stillbirth and fetal growth restriction - a systematic review.探讨不明原因绒毛膜炎与死胎和胎儿生长受限的关系——一项系统评价。
Placenta. 2013 Oct;34(10):856-62. doi: 10.1016/j.placenta.2013.07.003. Epub 2013 Jul 30.
10
The immunological basis of villitis of unknown etiology - review.不明病因绒毛膜炎的免疫学基础 - 综述。
Placenta. 2013 Oct;34(10):846-55. doi: 10.1016/j.placenta.2013.07.002. Epub 2013 Jul 26.

上调不明病因绒毛膜炎胎盘组织中 HLA-I 类和 II 类分子的表达。

Upregulation of HLA-Class I and II in Placentas Diagnosed with Villitis of Unknown Etiology.

机构信息

Department of Obstetrics and Gynecology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Department of Health Science Research, Mayo Clinic, Rochester, MN, USA.

出版信息

Reprod Sci. 2020 May;27(5):1129-1138. doi: 10.1007/s43032-019-00101-9. Epub 2020 Jan 6.

DOI:10.1007/s43032-019-00101-9
PMID:32046454
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7255550/
Abstract

The placenta utilizes many mechanisms to protect the haploidentical fetus from recognition by the maternal immune system. However, in cases of villitis of unknown etiology (VUE), maternal lymphocytes gain access into the placenta, causing significant health risks for the fetus. Evidence suggests that VUE is a rejection response between the mother and the haploidentical fetus. Therefore, we profiled human leukocyte antigen (HLA), an important predictor of transplant rejection, in VUE using placental tissue from ten patients with VUE and ten gestational age matched controls. Placentas were stained using novel multiplexed immunofluorescence (MxIF) to investigate morphology and HLA classes I and II. Gene expression was evaluated by microarray, and where available, tissue typing of mother/baby pairs was completed to determine HLA type. MxIF demonstrated strong CD8+ T cell infiltration and HLA class I staining both the distal and stem villi of VUE placentas. Compared to controls, VUE cases had significantly higher expression of HLA class II mRNA and pathway analysis demonstrated that 40% of the differentially expressed genes in VUE are related to tissue rejection. The data suggest that VUE resembles a rejection response between the mother and the fetus. It remains unknown what initiates immune recognition and why some mothers appear to be at higher risk for developing this condition than others. Understanding this etiology will be critical for developing effective interventions or prevention strategies during pregnancy.

摘要

胎盘利用多种机制来保护单倍体胎儿免受母体免疫系统的识别。然而,在原因不明的绒毛膜炎(VUE)的情况下,母体淋巴细胞进入胎盘,对胎儿造成重大健康风险。有证据表明,VUE 是母体和单倍体胎儿之间的排斥反应。因此,我们使用 10 例 VUE 患者和 10 例孕龄匹配对照的胎盘组织,对 VUE 中的人类白细胞抗原(HLA)进行了分析,HLA 是移植排斥的重要预测因子。通过新型多重免疫荧光(MxIF)对胎盘进行染色,以研究形态和 HLA I 类和 II 类。通过微阵列评估基因表达,并且在可用的情况下,完成了母亲/婴儿对的组织分型以确定 HLA 类型。MxIF 显示出强烈的 CD8+T 细胞浸润和 HLA I 类染色,均在 VUE 胎盘的远端和干绒毛中。与对照组相比,VUE 病例的 HLA II 类 mRNA 表达显著升高,并且通路分析表明,VUE 中 40%的差异表达基因与组织排斥有关。数据表明,VUE 类似于母体和胎儿之间的排斥反应。目前尚不清楚是什么引发了免疫识别,以及为什么有些母亲似乎比其他母亲更容易出现这种情况。了解这种病因对于在怀孕期间开发有效的干预或预防策略至关重要。