Regulatory T cells in embryo implantation and the immune response to pregnancy

被引:340
作者
Robertson, Sarah A.
Care, Alison S.
Moldenhauer, Lachlan M.
机构
[1] Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia
[2] Univ Adelaide, Adelaide Med Sch, Adelaide, SA, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
MATERNAL-FETAL INTERFACE; IN-VITRO FERTILIZATION; NATURAL-KILLER-CELLS; RECURRENT SPONTANEOUS-ABORTION; TRANSCRIPTION FACTOR FOXP3; GROWTH-FACTOR-BETA; PERIPHERAL-BLOOD; DENDRITIC CELLS; SEMINAL PLASMA; CD4(+) CD25(+);
D O I
10.1172/JCI122182
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
At implantation, the embryo expresses paternally derived alloantigens and evokes inflammation that can threaten reproductive success. To ensure a robust placenta and sustainable pregnancy, an active state of maternal immune tolerance mediated by CD4(+) regulatory T cells (Tregs) is essential. Tregs operate to inhibit effector immunity, contain inflammation, and support maternal vascular adaptations, thereby facilitating trophoblast invasion and placental access to the maternal blood supply. Insufficient Treg numbers or inadequate functional competence are implicated in idiopathic infertility and recurrent miscarriage as well as later-onset pregnancy complications stemming from placental insufficiency, including preeclampsia and fetal growth restriction. In this Review, we summarize the mechanisms acting in the conception environment to drive the Treg response and discuss prospects for targeting the T cell compartment to alleviate immune-based reproductive disorders.
引用
收藏
页码:4224 / 4235
页数:12
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