Habets W J, de Rooij D J, Hoet M H, van de Putte L B, van Venrooij W J
Clin Exp Immunol. 1985 Feb;59(2):457-66.
A quantitative immunoblotting assay (QIBA) for the determination of specific antibody titres in human autoimmune sera is described. In this assay, a total HeLa nuclear protein fraction, immobilized on nitrocellulose blot strips, was used as source of antigens and immunoreactive species of autoantibodies were quantitated by an enzyme linked second antibody procedure. Besides being more discriminative, QIBA appeared to be up to 500 times more sensitive than immunodiffusion or immunoelectrophoresis. In this study we used 21 sera from patients with SLE or MCTD for a quantitative analysis of their specific autoantibody content. Within this group, a very diverse spectrum of antibody populations was observed; anti-RNP sera appeared to contain, among others, high tired antibody versus 70K and 31K polypeptides while all (n = 6) anti-Sm sera recognized a 25kD protein doublet. In a follow-up study of two MCTD patients significant flares in specific antibody content could be observed.
本文描述了一种用于测定人自身免疫血清中特异性抗体滴度的定量免疫印迹分析(QIBA)方法。在该分析中,固定在硝酸纤维素印迹条上的总HeLa核蛋白组分用作抗原来源,通过酶联二抗程序对自身抗体的免疫反应性种类进行定量。除了具有更高的鉴别能力外,QIBA的灵敏度似乎比免疫扩散或免疫电泳高500倍。在本研究中,我们使用了21份来自系统性红斑狼疮(SLE)或混合性结缔组织病(MCTD)患者的血清,对其特异性自身抗体含量进行了定量分析。在该组中,观察到了非常多样化的抗体群体谱;抗核糖核蛋白(RNP)血清似乎除其他外,含有针对70K和31K多肽的高滴度抗体,而所有(n = 6)抗史密斯(Sm)血清均识别一种25kD的蛋白双峰。在对两名MCTD患者的随访研究中,可以观察到特异性抗体含量的显著波动。