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新生儿重症肌无力及去半乳糖基IgG的作用。

Neonatal myasthenia gravis and the role of agalactosyl IgG.

作者信息

Pilkington C, Lefvert A K, Rook G A

机构信息

Department of Medical Microbiology, UCL Medical School, London.

出版信息

Autoimmunity. 1995;21(2):131-5. doi: 10.3109/08916939508993361.

DOI:10.3109/08916939508993361
PMID:8679902
Abstract

Neonatal autoimmune diseases are thought to be due to the transfer of maternal autoantibodies. However, there is a puzzling lack of correlation between maternal autoantibody titres and disease in the neonate. So far, no factor reliably predictive of neonatal disease has been found. Agalactosyl IgG is a variable feature of normal IgG. Preliminary studies indicated that the percentage of agalactosyl IgG is lower in the serum of normal neonates, than in the serum of the mother at delivery. Since raised % agalactosyl IgG is often associated with autoimmune disease we sought to determine whether this relationship holds true in a neonatal autoimmune disease. We measured the % agalactosyl IgG in paired maternal-cord sera from patients with myasthenia gravis, some of whom had offspring with neonatal myasthenia gravis. We found that the percentage of agalactosyl IgG was significantly higher in affected than in unaffected neonates. Moreover % agalactosyl IgG was higher in sera of affected neonates than in serum from their mothers, while unaffected infants of mothers with myasthenia had %Gal(0) lower than their mothers, mimicking the normal situation. This suggests that in affected neonates a high proportion of the IgG is synthesised by the baby itself rather than derived from the mother. This agrees with previous evidence based on the presence of idiotypes not found in the mother which implied that the neonates with neonatal myasthenia gravis produce their own autoantibodies.

摘要

新生儿自身免疫性疾病被认为是由于母体自身抗体的转移所致。然而,母体自身抗体滴度与新生儿疾病之间令人困惑地缺乏相关性。到目前为止,尚未发现可靠预测新生儿疾病的因素。无半乳糖基IgG是正常IgG的一个可变特征。初步研究表明,正常新生儿血清中无半乳糖基IgG的百分比低于分娩时母亲血清中的百分比。由于升高的无半乳糖基IgG百分比常与自身免疫性疾病相关,我们试图确定这种关系在新生儿自身免疫性疾病中是否成立。我们测量了重症肌无力患者母婴配对血清中的无半乳糖基IgG百分比,其中一些患者的后代患有新生儿重症肌无力。我们发现,患病新生儿中无半乳糖基IgG的百分比显著高于未患病新生儿。此外,患病新生儿血清中的无半乳糖基IgG百分比高于其母亲的血清,而重症肌无力母亲的未患病婴儿的无半乳糖基IgG百分比低于其母亲,这与正常情况相似。这表明,在患病新生儿中,很大一部分IgG是由婴儿自身合成的,而非来自母亲。这与之前基于母亲体内未发现的独特型的存在而得出的证据一致,该证据表明患有新生儿重症肌无力的新生儿会产生自己的自身抗体。

相似文献

1
Neonatal myasthenia gravis and the role of agalactosyl IgG.新生儿重症肌无力及去半乳糖基IgG的作用。
Autoimmunity. 1995;21(2):131-5. doi: 10.3109/08916939508993361.
2
Agalactosyl IgG and antibody specificity in rheumatoid arthritis, tuberculosis, systemic lupus erythematosus and myasthenia gravis.类风湿关节炎、结核病、系统性红斑狼疮和重症肌无力中的无半乳糖基IgG及抗体特异性
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Neonatal myasthenia gravis: clinical and immunological study of seven mothers and their newborn infants.新生儿重症肌无力:7名母亲及其新生儿的临床与免疫学研究。
J Neuroimmunol. 1986 Aug;12(2):155-61. doi: 10.1016/0165-5728(86)90028-7.
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Agalactosyl IgG and materno-fetal transmission of autoimmune neonatal lupus.
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Anti-idiotypic antibodies against the receptor antibodies in myasthenia gravis.针对重症肌无力中受体抗体的抗独特型抗体。
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Antiacetylcholine receptor antibody in neonatal myasthenia gravis.新生儿重症肌无力中的抗乙酰胆碱受体抗体
Am J Dis Child. 1981 Mar;135(3):222-6. doi: 10.1001/archpedi.1981.02130270014006.
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Newborn infants to myasthenic mothers: a clinical study and an investigation of acetylcholine receptor antibodies in 17 children.重症肌无力母亲的新生儿:一项针对17名儿童的临床研究及乙酰胆碱受体抗体调查
Neurology. 1983 Feb;33(2):133-8. doi: 10.1212/wnl.33.2.133.
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Neonatal myasthenia gravis: antigenic specificities of antibodies in sera from mothers and their infants.新生儿重症肌无力:母亲及其婴儿血清中抗体的抗原特异性
Clin Exp Immunol. 1990 Jun;80(3):376-80. doi: 10.1111/j.1365-2249.1990.tb03296.x.
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Alpha-bungarotoxin blocking antibodies in neonatal myasthenia gravis: frequency and selectivity.新生儿重症肌无力中的α-银环蛇毒素阻断抗体:频率与选择性
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Autoantiidiotypic antibodies in myasthenia gravis.重症肌无力中的自身抗独特型抗体。
Ann N Y Acad Sci. 1987;505:133-54. doi: 10.1111/j.1749-6632.1987.tb51288.x.

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2
Agalactosyl IgG and materno-fetal transmission of autoimmune neonatal lupus.
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