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受精、着床和妊娠期间胎儿特异性 T 细胞的调节。

Fetus specific T cell modulation during fertilization, implantation and pregnancy.

机构信息

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Placenta. 2011 Oct;32 Suppl 4:S291-7. doi: 10.1016/j.placenta.2011.03.014. Epub 2011 May 17.

Abstract

Recently there is an increasing interest in aspects of a more specific immunoregulation during pregnancy. Understanding these mechanism might have a broader application not only for reproductive immunology but also in general for biology and medicine. Especially the induction, already before conception, of feto-specific T cells with a possibly regulatory function gives a biological explanation of local immunotolerance at the maternal fetal interface, supporting the epidemiological evidence of a feto/paternal-specific immuneregulation. Understanding the expression of specific HLA-classes on trophoblast and the crosstalk of these antigens with various cell types, specifically modulated in the decidua, resulting in the secretion of cytokines and (angiogenic) chemokines has given us a more and more detailed understanding of this regulation. This regulation could be induced by fetal cells circulating in the mother (microchimerism) and from the interaction with fetal subcellular fractions as exosomes, but also from paternal antigens present in seminal fluid. Molecular interaction between paternal and fetal antigens and receptors in endometrium and the decidua are discussed. This review highlights besides uNK cells, especially the function of CD4+ and CD8+ T cells with a regulatory function in the context of recurrent miscarriage and pre-eclampsia. Besides HLA, also male-specific minor histocompatibility antigens and the genetic background for these pregnancy complications are discussed.

摘要

最近,人们对妊娠期间更具体的免疫调节方面越来越感兴趣。了解这些机制不仅可能对生殖免疫学有更广泛的应用,而且对生物学和医学也有广泛的应用。特别是在受孕前诱导具有可能的调节功能的胎儿特异性 T 细胞,为母胎界面的局部免疫耐受提供了生物学解释,支持了胎儿/父系特异性免疫调节的流行病学证据。理解滋养层上特定 HLA 类别的表达以及这些抗原与各种细胞类型的相互作用,特别是在蜕膜中被特异性调节,导致细胞因子和(血管生成)趋化因子的分泌,使我们对这种调节有了越来越详细的理解。这种调节可以通过在母亲体内循环的胎儿细胞(微嵌合体)和与胎儿亚细胞部分(如外泌体)的相互作用来诱导,也可以通过存在于精液中的父系抗原来诱导。讨论了子宫内膜和蜕膜中父系和胎儿抗原与受体之间的分子相互作用。除了 uNK 细胞外,本文还特别强调了具有调节功能的 CD4+和 CD8+T 细胞在复发性流产和子痫前期中的作用。除了 HLA 之外,还讨论了男性特异性次要组织相容性抗原以及这些妊娠并发症的遗传背景。

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