Regulatory T Cells and Their Role in Pregnancy

被引:121
作者
Leber, Anne [1 ]
Teles, Ana [1 ]
Zenclussen, Ana C. [1 ]
机构
[1] Otto VonGuericke Univ Magdegurg, Dept Expt Obstet & Gynecol, Fac Med, D-39108 Magdeburg, Germany
关键词
Treg; pregnancy; tolerance; TRANSCRIPTION FACTOR FOXP3; FETAL-MATERNAL INTERFACE; IMMUNOLOGICAL SELF-TOLERANCE; ABORTION-PRONE MATINGS; DENDRITIC CELLS; PERIPHERAL-BLOOD; HUMAN ENDOMETRIUM; MURINE PREGNANCY; MENSTRUAL-CYCLE; CD28; SUPERAGONISTS;
D O I
10.1111/j.1600-0897.2010.00821.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells emerge in the last years as key players in allowing fetal survival within the maternal uterus. They were shown to be a unique subpopulation of T cells expanding during human and murine pregnancy. The importance of Treg for a normal pregnancy situation was proven by studies showing that their absence impairs murine pregnancy while the adoptive transfer of Treg prevents fetal rejection. In humans, pregnancy pathologies are associated with lower Treg frequencies while therapies that improve pregnancy outcome are able to boost their number. Functional studies have shown that Treg can regulate immune cell responses directly at the fetal-maternal interface either by interacting with other cells or by inducing the expression of immune regulatory molecules. This article revises relevant literature on regulatory T cells in human and murine pregnancy.
引用
收藏
页码:445 / 459
页数:15
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