HLA-G: At the Interface of Maternal-Fetal Tolerance

被引:196
作者
Ferreira, Leonardo M. R. [1 ,2 ]
Meissner, Torsten B. [1 ]
Tilburgs, Tamara [1 ]
Strominger, Jack L. [1 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
NATURAL-KILLER-CELLS; HUMAN DECIDUAL MACROPHAGES; REGULATORY T-CELLS; G MESSENGER-RNA; G EXPRESSION; G GENE; TRANSCRIPTIONAL REGULATION; TROPHOBLAST CELLS; NK CELLS; INDOLEAMINE 2,3-DIOXYGENASE;
D O I
10.1016/j.it.2017.01.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During pregnancy, semiallogeneic fetal extravillous trophoblasts (EVT) invade the uterine mucosa without being rejected by the maternal immune system. Several mechanisms were initially proposed by Peter Medawar half a century ago to explain this apparent violation of the laws of transplantation. Then, three decades ago, an unusual human leukocyte antigen (HLA) molecule was identified: HLA-G. Uniquely expressed in EVT, HLA-G has since become the center of the present understanding of fetus-induced immune tolerance. Despite slow progress in the field, the last few years have seen an explosion in our knowledge of HLA-G biology. Here, we critically review new insights into the mechanisms controlling the expression and function of HLA-G at the maternal-fetal interface, and discuss their relevance for fetal tolerance.
引用
收藏
页码:272 / 286
页数:15
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