Aitkaci A, Monier J C, Mamelle N
J Immunol Methods. 1981;44(3):311-22. doi: 10.1016/0022-1759(81)90049-1.
We describe an enzyme-linked immunosorbent assay (ELISA) with adsorption of histones (total and fractions) on glass beads and saturation of excess sites with sheep serum. The anti-histone antibodies are detected with peroxidase conjugate and developed with Trinder's reagent which has great stability. This very sensitive method detects anti-histone antibodies in 53% of SLE patients and in virtually no other diseases. Positive reactions are observed only with total histones and fractions H1 and H2b.
我们描述了一种酶联免疫吸附测定法(ELISA),该方法将组蛋白(总组蛋白和各组分)吸附在玻璃珠上,并用羊血清使多余位点饱和。用辣根过氧化物酶结合物检测抗组蛋白抗体,并用稳定性极佳的Trinder试剂显色。这种非常灵敏的方法在53%的系统性红斑狼疮(SLE)患者中检测到抗组蛋白抗体,而在几乎其他疾病中未检测到。仅在总组蛋白以及H1和H2b组分中观察到阳性反应。