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新生儿重症肌无力中的抗乙酰胆碱受体抗体

Antiacetylcholine receptor antibody in neonatal myasthenia gravis.

作者信息

Donaldson J O, Penn A S, Lisak R P, Abramsky O, Brenner T, Schotland D L

出版信息

Am J Dis Child. 1981 Mar;135(3):222-6. doi: 10.1001/archpedi.1981.02130270014006.

Abstract

Maternal titers to antiacetylcholine receptor antibody (anti-AChR Ab) were higher in two mothers with myasthenia gravis (MG) who had infants with neonatal MG than the nearly normal values in two mothers with MG who had unaffected infants. In one unaffected infant, another IgG antibody crossed the placenta, but an IgM antibody did not. In neonates there seems to be a correlation between the concentration of anti-AChR Ab and the presence and severity of the neonatal syndrome. The absence of fetal symptoms of MG and the delayed onset or worsening of some cases of neonatal MG may be due to high fetal levels of alpha-fetoprotein and its decline in concentration in infants after birth.

摘要

患有重症肌无力(MG)且婴儿患新生儿重症肌无力的两位母亲,其抗乙酰胆碱受体抗体(抗AChR Ab)的母源滴度高于患有MG但婴儿未受影响的两位母亲的接近正常水平。在一名未受影响的婴儿中,另一种IgG抗体穿过了胎盘,但IgM抗体未穿过。在新生儿中,抗AChR Ab的浓度与新生儿综合征的存在及严重程度之间似乎存在关联。MG胎儿症状的缺失以及部分新生儿MG病例的延迟发作或病情恶化,可能是由于胎儿体内甲胎蛋白水平较高,且出生后婴儿体内其浓度下降所致。

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