Jarvis J N, Moore H T, Fine N, Berry S M
Department of Pediatrics, Wayne State University School of Medicine, Detroit, MI, USA.
Biol Neonate. 1996;69(4):225-9. doi: 10.1159/000244314.
Since the fetus is semiallogenic to the mother, mechanisms have evolved to protect fetal tissue from the maternal immune response. Among these mechanisms is the expression of cell-surface complement regulatory proteins at the maternal-fetal interface. However, beginning in the third trimester, fetal blood cells are exposed to actively-transported IgG antibody. Thus, we speculated that fetal blood cells would require expression of one or more complement regulators by the early third trimester. Using flow cytometry and Western blots, we have demonstrated the presence of three important complement regulatory proteins in the circulating blood cells of human fetuses. These findings are consistent with the putative biological role of the cell-surface complement regulatory proteins.
由于胎儿对母亲来说是半同种异体的,因此已经进化出一些机制来保护胎儿组织免受母体免疫反应的影响。这些机制之一是在母胎界面处表达细胞表面补体调节蛋白。然而,从妊娠晚期开始,胎儿血细胞会接触到主动转运的IgG抗体。因此,我们推测胎儿血细胞在妊娠晚期早期就需要表达一种或多种补体调节因子。通过流式细胞术和蛋白质免疫印迹法,我们已经证实在人类胎儿的循环血细胞中存在三种重要的补体调节蛋白。这些发现与细胞表面补体调节蛋白的假定生物学作用一致。