Circulating Cytokines and Alarmins Associated with Placental Inflammation in High-Risk Pregnancies

被引:69
作者
Girard, Sylvie [1 ,2 ,3 ]
Heazell, Alexander E. P. [1 ,2 ]
Derricott, Hayley [1 ,2 ]
Allan, Stuart M. [3 ]
Sibley, Colin P. [1 ,2 ]
Abrahams, Vikki M. [4 ]
Jones, Rebecca L. [1 ,2 ]
机构
[1] Univ Manchester, Maternal & Fetal Hlth Res Ctr, Inst Human Dev, Fac Med & Human Sci, Manchester, Lancs, England
[2] Cent Manchester Univ Hosp NHS Fdn Trust, St Marys Hosp, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
[3] Univ Manchester, Fac Life Sci, Manchester, Lancs, England
[4] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT USA
基金
英国惠康基金;
关键词
High-risk pregnancy; inflammation; placental dysfunction; stillbirth; PRETERM BIRTH; FETAL DNA; INFECTION; DEATH; WOMEN; LABOR;
D O I
10.1111/aji.12274
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Problem Inflammation during pregnancy has devastating consequences for the placenta and fetus. These events are incompletely understood, thereby hampering screening and treatment. Method of studyThe inflammatory profile of villous tissue was studied in pregnancies at high-risk of placental dysfunction and compared to uncomplicated pregnancies. The systemic inflammatory profile was assessed in matched maternal serum samples in cases of reduced fetal movements (RFM). ResultsPlacentas from RFM pregnancies had a unique inflammatory profile characterized by increased interleukin (IL)-1 receptor antagonist and decreased IL-10 expression, concomitant with increased numbers of placental macrophages. This aberrant cytokine profile was evident in maternal serum in RFM, as were increased levels of alarmins (uric acid, HMGB1, cell-free fetal DNA). ConclusionThis distinct inflammatory profile at the maternal-fetal interface, mirrored in maternal serum, could represent biomarkers of placental inflammation and could offer novel therapeutic options to protect the placenta and fetus from an adverse maternal environment.
引用
收藏
页码:422 / 434
页数:13
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