Revillard J P
Bull Cancer. 1979;66(2):115-25.
The essential information about materno-foetal immunologic interactions is reviewed. After a brief description of placental tissue (decidual cells from uterine mucosa, trophoblast), evidence that immunisation can be achieved by introduction of antigen into normal uterus is presented, although grafts performed in uterus of pregnant females are prolonged. Throphoblast cells bear specific antigens but histocompatibility antigens are usually not detectable at their surface. Proteins and cells from the foetus enter the maternal circulation and vice-versa, resulting in the production of antibodies against cell-associated foetal antigens by the mother. Some regulatory process of the maternal immune response have been investigated including blocking antibodies, maternal and foetal suppressor T cells. The biological roles of trophoblast and that of sustained microchimerism are underlined. Immunologic damage to the foetus can be produced only by inducing a cytotoxic cellular response before pregnancy. Possible analogies between immune responses to foetal allografts and tumors are discussed.
本文综述了母胎免疫相互作用的基本信息。在简要描述胎盘组织(来自子宫黏膜的蜕膜细胞、滋养层细胞)之后,尽管在怀孕雌性子宫中进行的移植会延长,但有证据表明将抗原引入正常子宫可实现免疫。滋养层细胞带有特定抗原,但其表面通常检测不到组织相容性抗原。胎儿的蛋白质和细胞进入母体循环,反之亦然,导致母亲产生针对细胞相关胎儿抗原的抗体。已经研究了母体免疫反应的一些调节过程,包括封闭抗体、母体和胎儿抑制性T细胞。强调了滋养层的生物学作用以及持续微嵌合体的作用。只有在怀孕前诱导细胞毒性细胞反应,才会对胎儿产生免疫损伤。讨论了对胎儿同种异体移植和肿瘤的免疫反应之间可能的相似之处。