首页> 美国卫生研究院文献>Clinical and Experimental Immunology >A common anti-cardiolipin antibody idiotype in autoimmune disease: identification using a mouse monoclonal antibody directed against a naturally-occurring anti-phospholipid antibody.
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A common anti-cardiolipin antibody idiotype in autoimmune disease: identification using a mouse monoclonal antibody directed against a naturally-occurring anti-phospholipid antibody.

机译:自身免疫性疾病中常见的抗心磷脂抗体独特型:使用针对天然存在的抗磷脂抗体的小鼠单克隆抗体进行鉴定。

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摘要

We have recently produced a series of human monoclonal antibodies reacting with cardiolipin. One of these, H3, a polyspecific IgM/k derived from a normal individual, was used to raise mouse monoclonal antibody to its idiotype. Two anti-idiotypic antibodies, S2.9 (IgG2b) and S2.10 (IgM) were selected for their specific reaction with H3.S2.9 did not react with five other human monoclonal antibodies of IgM/k class despite the fact that these shared some antigen-binding characteristics with H3.S2.9 was able to block the binding of H3 to all of its cross-reactive antigens including cardiolipin, while S2.10 was not. S2.9 was equally efficient in blocking the binding of H3 to three of its cross-reactive antigens, cardiolipin, diphtheria and tetanus toxoids; greater than 90% inhibition could be achieved at an equimolar ratio of H3 to S2.9. The anti-idiotype S2.9 was used to demonstrate the presence of the H3 idiotype in serum. This idiotype was found in amounts greater than that seen in 42 normal individuals, in 30 of 36 patients with systemic lupus erythematosus (SLE), eight of 20 patients with rheumatoid arthritis (RA), 8 of 20 patients with Felty's syndrome as well as 10 of 23 patients with syphilis. Not one of nine patients with drug-induced lupus syndrome had abnormal levels. In patients with SLE and Felty's syndrome there was a good correlation between the amount of anti-cardiolipin antibodies and the amount of H3 idiotype (rs = 0.70 and 0.69 respectively). No such correlation was found in syphilitics or in patients with RA. In patients with SLE the H3 idiotype was present on IgM and IgG anti-cardiolipin antibodies. In 15 of 16 SLE sera with high levels of cardiolipin antibody, S2.9 blocked binding of serum antibodies to cardiolipin by 13-72%, with a mean value of 49%. One patient had a high level of anti-cardiolipin antibody which could not be blocked by S2.9. These results indicate that a mouse monoclonal antibody which reacts with an idiotope in the antigen-binding region of a naturally-occurring phospholipid antibody also defines a common idiotype of anti-cardiolipin antibodies in patients with autoimmune disease.
机译:我们最近生产了一系列与心磷脂反应的人单克隆抗体。其中之一,H3,一种来自正常个体的多特异性IgM / k,被用于产生小鼠单克隆抗体使其独特型。选择了两种抗独特型抗体S2.9(IgG2b)和S2.10(IgM)与H3进行特异性反应.S2.9不会与其他五种IgM / k类人单克隆抗体发生反应与H3具有某些抗原结合特性。S2.9能够阻断H3与所有其交叉反应性抗原(包括心磷脂)的结合,而S2.10则不能。 S2.9同样有效地阻断了H3与其三种交叉反应抗原的结合,即心磷脂,白喉和破伤风类毒素。当H3与S2.9等摩尔比时,可实现90%以上的抑制作用。抗独特型S2.9用于证明血清中存在H3独特型。在36例系统性红斑狼疮(SLE)患者中有30例,20例类风湿关节炎(RA)患者中有8例,在20例Felty's综合征患者中有8例以及10例中发现了这种独特型,其数量高于42例正常个体23例梅毒患者。九名药物性狼疮综合征患者中,没有一个患者的异常水平。在患有SLE和Felty综合征的患者中,抗心磷脂抗体的数量与H3独特型的数量之间具有良好的相关性(分别为0.70和0.69)。在梅毒或RA患者中未发现这种相关性。在SLE患者中,H3独特型存在于IgM和IgG抗心磷脂抗体上。在心磷脂抗体水平高的16个SLE血清中,有15个S2.9阻止血清抗体与心磷脂的结合达到13-72%,平均值为49%。一名患者的抗心磷脂抗体水平很高,无法被S2.9阻断。这些结果表明,与天然存在的磷脂抗体的抗原结合区域中的独特型反应的小鼠单克隆抗体在自身免疫性疾病患者中也定义了抗心磷脂抗体的独特型。

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