The role of indoleamine-2,3-dioxygenase in normal and pathological pregnancies

被引:50
作者
Chang, Rui-Qi [1 ]
Li, Da-Jin [1 ,2 ,3 ]
Li, Ming-Qing [1 ,2 ,3 ]
机构
[1] Fudan Univ, Lab Reprod Immunol, Hosp Obstet & Gynecol, Shanghai, Peoples R China
[2] Fudan Univ, Key Lab Reprod Regulat NPFPC, IRD, SIPPR, Shanghai, Peoples R China
[3] Shanghai Key Lab Female Reprod Endocrine Related, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
immunosuppression; indoleamine-2; 3-dioxygenase; normal pregnancy; preeclampsia; preterm labor; recurrent spontaneous abortion; REGULATORY T-CELLS; RECURRENT SPONTANEOUS-ABORTION; ARYL-HYDROCARBON RECEPTOR; PLACENTAL INDOLEAMINE 2,3-DIOXYGENASE; ALLOGENEIC FETAL REJECTION; INNATE LYMPHOID-CELLS; DENDRITIC CELLS; TRYPTOPHAN CATABOLISM; IDO EXPRESSION; 3-DIOXYGENASE EXPRESSION;
D O I
10.1111/aji.12786
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The survival of allogeneic fetus during pregnancy contradicts the laws of immune responses. Behind this paradoxical phenomenon, the mechanism is quite complex. Indoleamine-2,3-dioxygenase (IDO) is the first and rate-limiting enzyme of tryptophan catabolism. Emerging evidence shows that IDO is expressed at the maternal-fetal interface, including trophoblast cells, decidual stroma cells, decidual immune cells (eg, natural killer cells, T cells, and macrophages), and vascular endothelial cells of decidua and chorion. Moreover, the expression and activity of IDO are different among non-pregnant, normal pregnant, and pathological pregnant conditions. IDO plays important roles in normal pregnancy through immune suppression and regulation of fetal invasion and circulation. However, the abnormal expression and dysfunction of IDO are associated with some pathological pregnancies (including recurrent spontaneous abortion, preeclampsia, preterm labor, and fetal growth restriction).
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页数:9
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