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

被引:0
|
作者
Elizabeth Ann L. Enninga
Alexey A. Leontovich
Bohdana Fedyshyn
Laurie Wakefield
Manish Gandhi
Svetomir N. Markovic
Rodrigo Ruano
Sarah E. Kerr
机构
[1] Mayo Clinic,Department of Obstetrics and Gynecology
[2] Mayo Clinic,Department of Health Science Research
[3] Mayo Clinic,Department of Transfusion Medicine
[4] Mayo Clinic,Department of Immunology
[5] Mayo Clinic,Department of Laboratory Pathology
来源
Reproductive Sciences | 2020年 / 27卷
关键词
Placenta; HLA; Villitis; Inflammation; Rejection;
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学科分类号
摘要
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.
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页码:1129 / 1138
页数:9
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