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狼疮性脑病活动期狼疮患者抗单链DNA抗体上非活动期抗双链DNA独特型的表达

Expression of inactive stage anti-dsDNA idiotypes on anti-ssDNA antibodies in a lupus patient during active stage of lupus cerebritis.

作者信息

Suenaga R, Abdou N I

机构信息

Immunology Research Laboratory, St. Luke's Hospital, Kansas City, MO 64111.

出版信息

J Autoimmun. 1992 Jun;5(3):379-92. doi: 10.1016/0896-8411(92)90150-o.

Abstract

The possibility that idiotypes (Ids) defined on anti-double stranded DNA (dsDNA) antibodies during active and inactive stages of lupus (1/84 Id and 4/90 Id, respectively) were expressed on anti-DNA antibodies during a subsequent active period (9/90) of the disease was investigated in a lupus patient with lupus cerebritis. Using rabbit (R)-anti-Ids specific to 1/84 Id and 4/90 Id in inhibition assays, the 4/90 Id was shown to be expressed on the framework regions of anti-single stranded DNA (ssDNA) but poorly on co-existing anti-dsDNA antibodies of active (9/90) stage. The 1/84 Id was poorly expressed on both types of 9/90 anti-DNA antibodies. While the 9/90 anti-ssDNA significantly bound to immobilized ssDNA and several single-stranded polynucleotides, only ssDNA inhibited the binding of the anti-ssDNA to ssDNA, suggesting its monospecificity toward ssDNA. Western blot analysis following isoelectric focusing showed that a spectrotype pattern of 4/90 Id-positive 9/90 anti-ssDNA IgG was similar to that of the 4/90 anti-dsDNA, suggesting that they are of related clonal origin. The present study suggests the idiotypic heterogeneity of anti-DNA antibodies and the shift of antigen specificity within an idiotypically related anti-DNA population during exacerbation of the disease.

摘要

在一名患有狼疮性脑病的狼疮患者中,研究了在狼疮活动期和非活动期(分别为1/84 Id和4/90 Id)定义的抗双链DNA(dsDNA)抗体上的独特型(Ids)在疾病随后的活动期(9/90)是否在抗DNA抗体上表达。在抑制试验中使用对1/84 Id和4/90 Id特异的兔(R)-抗Ids,结果显示4/90 Id在抗单链DNA(ssDNA)的构架区表达,但在活动期(9/90)共存的抗dsDNA抗体上表达较弱。1/84 Id在9/90型的两种抗DNA抗体上表达均较弱。虽然9/90抗ssDNA与固定化的ssDNA和几种单链多核苷酸有显著结合,但只有ssDNA能抑制抗ssDNA与ssDNA的结合,提示其对ssDNA具有单特异性。等电聚焦后的蛋白质印迹分析显示,4/90 Id阳性的9/90抗ssDNA IgG的光谱型模式与4/90抗dsDNA相似,提示它们具有相关的克隆起源。本研究提示抗DNA抗体的独特型异质性以及在疾病加重期间独特型相关抗DNA群体内抗原特异性的转变。

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