Persellin R H, Rhodes J
Clin Exp Immunol. 1981 Nov;46(2):350-4.
The precise factor responsible for the altered immunological reactivity and diminished inflammatory responses occurring in pregnancy is unknown. Recent observations implicate the pregnancy-associated alpha-2 glycoprotein (PAG). Using rosette assays for the detection of cells carrying Fc receptors and for the demonstration of surface HLA-DR antigens, we demonstrate that a serum protein fraction rich in PAG inhibits these surface markers on human monocytes. Brief exposure of normal peripheral blood monocytes to physiological concentrations of PAG led to almost total loss of Fc receptor expression, an effect that was concentration-related. Using a monoclonal anti-HLA-DR antibody linked to red cells, physiological concentrations of PAG also significantly inhibited the detection of HLA-DR on monocytes. As controls, we used a protein fraction isolated in identical fashion from male sera devoid of PAG, and an alpha-2 macroglobulin isolate. These findings suggest that PAG, by masking monocyte surface markers, could be responsible for the suppression of some cell functions during pregnancy.
目前尚不清楚导致孕期免疫反应改变和炎症反应减弱的确切因素。最近的观察结果表明,妊娠相关α-2糖蛋白(PAG)与此有关。我们使用玫瑰花结试验检测携带Fc受体的细胞并展示表面HLA-DR抗原,结果表明富含PAG的血清蛋白组分可抑制人单核细胞上的这些表面标志物。将正常外周血单核细胞短暂暴露于生理浓度的PAG会导致Fc受体表达几乎完全丧失,且该效应与浓度相关。使用与红细胞相连的单克隆抗HLA-DR抗体,生理浓度的PAG也能显著抑制单核细胞上HLA-DR的检测。作为对照,我们使用了以相同方式从不含PAG的男性血清中分离出的蛋白组分,以及一种α-2巨球蛋白分离物。这些发现表明,PAG通过掩盖单核细胞表面标志物,可能是孕期某些细胞功能受到抑制的原因。