Gliaschera M, Biver P, Brunori E, Romani L, Tarani A, de Luca Brunori I
Ann Ostet Ginecol Med Perinat. 1989 Jan-Feb;110(1):20-7.
Myasthenia gravis is an autoimmune disorder characterized by a reduction of muscular strength. It is associated with production of anti-acetylcholine-receptor antibodies and with the consequent decrease of muscular acetylcholine receptors. The Authors have studied this pathology during the pregnancy and the puerperium in a myasthenic patient and in her newborn, evaluating seric AChRAbs title and seric alpha-fetoprotein levels, to investigate the possible correlation among these parameters and MG. The study shows that with low seric levels of AChRAbs the mother had a progressive symptomatological impairment of MG from 36th week of pregnancy to term and in puerperium too; the newborn didn't show any sign of pathology. The possible immuno-protective role of alpha-FP in maternal and fetal MG evolution is discussed.
重症肌无力是一种自身免疫性疾病,其特征为肌肉力量减弱。它与抗乙酰胆碱受体抗体的产生以及随之而来的肌肉乙酰胆碱受体减少有关。作者研究了一名重症肌无力患者及其新生儿在妊娠和产褥期的这种病理情况,评估血清抗乙酰胆碱受体抗体水平和血清甲胎蛋白水平,以研究这些参数与重症肌无力之间可能存在的相关性。研究表明,母亲血清抗乙酰胆碱受体抗体水平较低,从妊娠第36周直至足月以及产褥期,重症肌无力的症状逐渐加重;新生儿未表现出任何病理迹象。本文讨论了甲胎蛋白在母婴重症肌无力病情发展中可能的免疫保护作用。