Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA; Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.
Trends Immunol. 2017 Apr;38(4):272-286. doi: 10.1016/j.it.2017.01.009. Epub 2017 Mar 6.
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.
在妊娠期间,半同种异体胎儿绒毛外滋养层细胞(EVT)会侵入子宫黏膜而不被母体免疫系统排斥。半个世纪前,Peter Medawar 最初提出了几种机制来解释这种明显违反移植法的现象。然后,三十年前,一种不寻常的人类白细胞抗原(HLA)分子被鉴定出来:HLA-G。HLA-G 仅在 EVT 中表达,此后成为目前对胎儿诱导免疫耐受的理解中心。尽管该领域进展缓慢,但在过去几年中,我们对 HLA-G 生物学的认识有了爆发式的增长。在这里,我们批判性地回顾了控制 HLA-G 在母体-胎儿界面表达和功能的机制的新见解,并讨论了它们与胎儿耐受的相关性。