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一种与小鼠和人类系统性红斑狼疮肾炎相关的保守抗DNA抗体独特型。

A conserved anti-DNA antibody idiotype associated with nephritis in murine and human systemic lupus erythematosus.

作者信息

Weisbart R H, Noritake D T, Wong A L, Chan G, Kacena A, Colburn K K

机构信息

Department of Medicine, Veterans Administration Medical Center, Sepulveda, CA 91343.

出版信息

J Immunol. 1990 Apr 1;144(7):2653-8.

PMID:2319132
Abstract

In order to identify unique structural features of pathogenic autoantibodies to DNA in SLE, a murine anti-anti-DNA (anti-Id) mAb (mAb 1C7) was produced in response to immunization of lupus mice with a syngeneic anti-DNA mAb (mAb 3E10). Immunization of lupus mice with mAb 3E10 inhibited production of native anti-DNA antibodies, suppressed development of lupus kidney disease (nephritis), and induced production of anti-anti-DNA (anti-Id) antibodies. mAb 1C7 bound F(ab')2 fragments of mAb 3E10, and it bound other murine anti-DNA mAb, but not murine mAb or polyclonal serum antibodies unreactive with DNA. Moreover, binding of mAb 1C7 anti-Id to mAb 3E10 was inhibited by DNA, suggesting anti-Id binding within or near the binding site for DNA. Furthermore, mAb 1C7 bound serum IgG immunoglobulins from 9/12 patients with lupus nephritis and serum anti-DNA antibodies compared to only 3/12 SLE patients with comparable serum levels of anti-DNA antibodies, but without nephritis (p = 0.04), and only 1/53 SLE patients without serum anti-DNA antibodies, 0/49 patients with rheumatoid arthritis, and 1/47 healthy subjects (p less than 0.001). These results provide evidence that mAb 1C7 identifies a conserved Id associated with anti-DNA antibodies in murine and human SLE and may be useful as a structural probe to characterize pathogenic anti-DNA antibodies in SLE.

摘要

为了识别系统性红斑狼疮(SLE)中针对DNA的致病性自身抗体的独特结构特征,通过用同基因抗DNA单克隆抗体(mAb 3E10)免疫狼疮小鼠,制备了一种鼠抗抗DNA(抗独特型)单克隆抗体(mAb 1C7)。用mAb 3E10免疫狼疮小鼠可抑制天然抗DNA抗体的产生,抑制狼疮性肾病(肾炎)的发展,并诱导抗抗DNA(抗独特型)抗体的产生。mAb 1C7与mAb 3E10的F(ab')2片段结合,也与其他鼠抗DNA单克隆抗体结合,但不与不与DNA反应的鼠单克隆抗体或多克隆血清抗体结合。此外,DNA可抑制mAb 1C7抗独特型与mAb 3E10的结合,提示抗独特型结合于DNA结合位点内或其附近。此外,mAb 1C7与12例狼疮性肾炎患者中的9例血清IgG免疫球蛋白及血清抗DNA抗体结合,而在12例具有相当血清抗DNA抗体水平但无肾炎的SLE患者中只有3例结合(p = 0.04),在53例无血清抗DNA抗体的SLE患者中只有1例结合,在49例类风湿关节炎患者中0例结合,在47例健康受试者中1例结合(p小于0.001)。这些结果证明mAb 1C7识别出与鼠和人SLE中抗DNA抗体相关的保守独特型,可能作为一种结构探针来表征SLE中致病性抗DNA抗体。

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