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定义人类类风湿因子上一个次要独特型和一个个体独特型的单克隆抗体。

Monoclonal antibodies defining a minor and a private idiotope on human rheumatoid factors.

作者信息

Pasquali J L, Storck D

出版信息

J Clin Immunol. 1986 Sep;6(5):349-54. doi: 10.1007/BF00915373.

Abstract

Two mouse monoclonal antibodies (mAb A216-5 and L 49-3) with antiidiotypic activity against two human monoclonal IgM rheumatoid factors (IgM RFs) were defined. Each of these monoclonal antibodies (two mouse IgG 1K) reacted with an idiotope located on the heavy chain of the immunizing monoclonal IgM RF and was able to inhibit RF fixation to the antigen. These monoclonal antibodies did not react with other monoclonal IgM RFs from patients with macroglobulinemias or cryoglobulinemias and, therefore, did not recognize the known cross-reactive idiotopes of human monoclonal RFs. The presence of both 216-5 and 49-3 idiotopes on polyclonal IgM RFs from unrelated patients was undetectable by the inhibition assays. However, using a four-stage solid-phase radioimmunoassay, the 216-5 idiotope (minor), but not the 49-3 idiotope (private), was frequently present at a low concentration on polyclonal IgM RFs from patients suffering from rheumatoid arthritis, primary Sjögren syndromes, various infectious diseases, systemic vasculitis, and sarcoidosis and during aging. Interestingly, the 216-5 idiotope was undetectable among polyclonal IgM RFs of 12 normal adults. The main conclusions of these data are the following. The definition of minor and private idiotopes of human RFs requires the use of assays able to detect low amounts of antibodies among polyclonal Ig. The anti-IgG B cells which are sometimes clonally expanded during Waldenström diseases and cryoglobulinemias can also be activated during nonneoplastic diseases, among the other RF-secreting B cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

确定了两种对两种人单克隆 IgM 类风湿因子(IgM RFs)具有抗独特型活性的小鼠单克隆抗体(单克隆抗体 A216 - 5 和 L 49 - 3)。这些单克隆抗体(两种小鼠 IgG 1K)中的每一种都与免疫单克隆 IgM RF 重链上的一个独特型表位发生反应,并且能够抑制 RF 与抗原的结合。这些单克隆抗体不与来自巨球蛋白血症或冷球蛋白血症患者的其他单克隆 IgM RFs 发生反应,因此,不识别已知的人单克隆 RFs 的交叉反应独特型表位。通过抑制试验无法检测到来自无关患者的多克隆 IgM RFs 上同时存在 216 - 5 和 49 - 3 独特型表位。然而,使用四阶段固相放射免疫测定法,216 - 5 独特型表位(次要的),而非 49 - 3 独特型表位(个体特异性的),在类风湿性关节炎、原发性干燥综合征、各种传染病、系统性血管炎和结节病患者以及衰老过程中的多克隆 IgM RFs 上经常以低浓度存在。有趣的是,在 12 名正常成年人的多克隆 IgM RFs 中未检测到 216 - 5 独特型表位。这些数据的主要结论如下。确定人 RFs 的次要和个体特异性独特型表位需要使用能够检测多克隆 Ig 中少量抗体的测定方法。在瓦尔登斯特伦病和冷球蛋白血症期间有时会发生克隆性扩增的抗 IgG B 细胞,在非肿瘤性疾病中,在其他分泌 RF 的 B 细胞中也可被激活。(摘要截短于 250 字)

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