Goshen E, Livne A, Nagy J, Sarov I, Shoenfeld Y
Corob Research Center, Department of Medicine D, Beer-Sheva, Israel.
Nephron. 1990;55(1):33-6. doi: 10.1159/000185915.
IgA nephropathy (IgAN), assumed to be a chronic immune complex glomerulonephritis, has been sometimes associated with various autoimmune diseases and autoimmune phenomena including autoantibody production. The current study was aimed at thoroughly investigating the frequency of raised autoantibody titers against five common nuclear autoantigens in a large number of patients with IgAN as well as patients with other primary immune complex glomerulopathies and normal controls. The incidence of autoantibodies (greater than 2 SD less than 3 SD of controls) in the IgAN group ranged between 13% in the case of anticardiolipin antibodies, and 19% in the case of antiribonucleoprotein antibodies, yet was not found to be significantly different from the incidence observed in the other control groups. In none of the subjects a titer above 3 SD of the means of controls was found. Our study clearly points to the fact that IgAN, while being an immune-mediated disease, is not a clear-cut autoimmune condition. The finding of autoantibodies in these patients may be merely incidental.
IgA肾病(IgAN)被认为是一种慢性免疫复合物性肾小球肾炎,有时与包括自身抗体产生在内的各种自身免疫性疾病和自身免疫现象相关。本研究旨在全面调查大量IgAN患者以及其他原发性免疫复合物性肾小球病患者和正常对照中针对五种常见核自身抗原的自身抗体滴度升高的频率。IgAN组中自身抗体(高于对照均值2个标准差且低于3个标准差)的发生率在抗心磷脂抗体情况下为13%,抗核糖核蛋白抗体情况下为19%,但未发现与其他对照组观察到的发生率有显著差异。在所有受试者中均未发现滴度高于对照均值3个标准差的情况。我们的研究清楚地表明,IgAN虽然是一种免疫介导的疾病,但并非典型的自身免疫性疾病。这些患者中自身抗体的发现可能仅仅是偶然的。