Israel E J, Simister N, Freiberg E, Caplan A, Walker W A
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Immunology. 1993 May;79(1):77-81.
In humans, the prenatal transfer of IgG from mother to foetus is facilitated by a receptor for IgG on the placenta. However, amniotic fluid contains IgG of maternal origin, and transfer of swallowed IgG into the circulation from the foetal intestine represents another potential pathway of passive immunization. In this study we assayed for a foetal intestinal IgG receptor to support the hypothesis of this alternate pathway of antibody transfer. Microvillous membrane (MVM) from small bowel of aborted foetuses (18 weeks gestation) were probed with [125I]IgG to detect specific IgG binding sites. Binding was pH dependent and was maximal at pH 6. Competitive inhibition of the binding of [125I]IgG was noted with the addition of increasing amounts of unlabelled IgG. Scatchard analysis showed one binding site with a dissociation constant of 1.58 x 10(-7), similar to that of the IgG receptor described on the suckling rat intestine. The binding of labelled IgG to the human MVM receptor was Fc mediated. These observations provide evidence for an Fc receptor on the human foetal intestine.
在人类中,胎盘上的IgG受体促进了IgG从母亲到胎儿的产前转移。然而,羊水含有母体来源的IgG,吞咽的IgG从胎儿肠道进入循环是被动免疫的另一种潜在途径。在本研究中,我们检测了胎儿肠道IgG受体,以支持这种抗体转移替代途径的假设。用[125I]IgG探测流产胎儿(妊娠18周)小肠的微绒毛膜(MVM),以检测特异性IgG结合位点。结合呈pH依赖性,在pH 6时最大。随着未标记IgG添加量的增加,观察到[125I]IgG结合的竞争性抑制。Scatchard分析显示有一个结合位点,解离常数为1.58×10^(-7),与哺乳大鼠肠道中描述的IgG受体相似。标记的IgG与人MVM受体的结合是由Fc介导的。这些观察结果为人类胎儿肠道上存在Fc受体提供了证据。