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新生儿狼疮综合征。

Neonatal lupus syndromes.

作者信息

Buyon J P

机构信息

Department of Rheumatic Diseases, Hospital for Joint Diseases, New York, NY 10003.

出版信息

Curr Opin Rheumatol. 1994 Sep;6(5):523-9. doi: 10.1097/00002281-199409000-00012.

Abstract

Neonatal lupus continues to generate considerable interest despite its rarity; more than 15 original contributions were made to the literature in the past year. Diverse aspects of this "syndrome" of passively acquired autoimmunity have been covered. Experiments using a rabbit model provided insights into the pathogenicity of maternal anti-Ro/SS-A and anti-La/SS-B antibodies. Perfusion of rabbit hearts with anti-Ro/SS-A and anti-La/SS-B sera resulted in conduction abnormalities in whole adult rabbit hearts and induced a reduction in the peak slow inward current in patch-clamp experiments of isolated rabbit ventricular myocytes, suggesting involvement of calcium channels. Clinical investigations are moving away from case reports, and recent studies now include substantial entries. Assuming that patients reported from the United States, Finland, and England are all separate, sera from at least 100 different mothers of infants with congenital heart block have been studied. Although there is apparently no serologic profile that is unique to mothers of affected children, compared with mothers of healthy children, anti-Ro/SS-A antibodies (anti-52-kD antibodies are more prevalent by immunoblot in congenital heart block, although all these sera are likely to have anti-60-kD antibodies by immunoprecipitation) are usually of high titer and associated with anti-La/SS-B antibodies. To date, the only maternal autoantibodies that have been associated with congenital heart block recognize Ro/SS-A or La/SS-B antigens. Mothers of affected infants are often asymptomatic, and when symptomatic, the clinical features are frequently characteristic of Sjögren's syndrome. Although treatment of affected fetuses with dexamethasone has successfully diminished associated effusions, there has been no report of reversal of established third-degree heart block.

摘要

尽管新生儿狼疮罕见,但它仍持续引发了相当大的关注;在过去一年里,有超过15篇原创文献发表。该“综合征”被动获得性自身免疫的多个方面都有涉及。使用兔模型的实验深入探讨了母体抗Ro/SS - A和抗La/SS - B抗体的致病性。用抗Ro/SS - A和抗La/SS - B血清灌注兔心脏,导致成年兔全心传导异常,并在分离的兔心室肌细胞的膜片钳实验中使慢内向电流峰值降低,提示钙通道参与其中。临床研究正从病例报告转向,近期研究现在纳入了大量病例。假设来自美国、芬兰和英国报告的患者都是不同个体,那么至少对100名患有先天性心脏传导阻滞婴儿的不同母亲的血清进行了研究。尽管显然没有一种血清学特征是受影响儿童母亲所特有的,但与健康儿童母亲相比,抗Ro/SS - A抗体(通过免疫印迹法,抗52 - kD抗体在先天性心脏传导阻滞中更普遍,尽管通过免疫沉淀法所有这些血清可能都有抗60 - kD抗体)通常滴度较高且与抗La/SS - B抗体相关。迄今为止,唯一与先天性心脏传导阻滞相关的母体自身抗体识别Ro/SS - A或La/SS - B抗原。受影响婴儿的母亲通常无症状,而有症状时,临床特征往往是干燥综合征的典型表现。尽管用地塞米松治疗受影响胎儿已成功减少了相关积液,但尚未有已确立的三度心脏传导阻滞逆转的报告。

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