Kuştimur S, Gülmezoğlu E
Mikrobiyol Bul. 1985 Oct;19(4):190-9.
In this study, antinuclear antibody (ANA), rheumatoid factor (RF) studied and IgA was determined with single radial immunodiffusion (RID) technic in the sera of 96 patients with systemic lupus erythematosus, 25 with rheumatoid arthritis and 100 normal individuals. In normal control group, the average level of IgA was found to be 212 mg/dl. In one patient (1: 100), IgA deficiency was detected with a level of 2.1 mg/dl, the average level of IgA in 96 patients with SLE was 320 +/- 16.25 mg/dl. In 3 patients of this group IgA deficiency was observed. According to this finding, the prevalence of IgA deficiency in the group of SLE ise 1: 32. This prevalence is higher than that of the normal population. The average level of IgA in 25 patients with RA 302.66 +/- 36.57 mg/dl. In this group we observed IgA deficiency only in one patient which means a prevalence of 1: 25, that is higher than the normal group. Reports indicate that the incidence of IgA deficiency in general populations may vary from 1: 400 up to 1: 3080. But in patients with SLE and RA, this may be encountered more frequently as we observed in our cases.
在本研究中,采用单向免疫扩散(RID)技术对96例系统性红斑狼疮患者、25例类风湿关节炎患者和100名正常个体的血清进行了抗核抗体(ANA)、类风湿因子(RF)检测,并测定了IgA。在正常对照组中,发现IgA的平均水平为212mg/dl。在1例患者(1:100)中,检测到IgA缺乏,水平为2.1mg/dl,96例系统性红斑狼疮患者的IgA平均水平为320±16.25mg/dl。该组中有3例患者观察到IgA缺乏。根据这一发现,系统性红斑狼疮组中IgA缺乏的患病率为1:32。这一患病率高于正常人群。25例类风湿关节炎患者的IgA平均水平为302.66±36.57mg/dl。在该组中,我们仅在1例患者中观察到IgA缺乏,这意味着患病率为1:25,高于正常组。报告表明,普通人群中IgA缺乏的发生率可能在1:400至1:3080之间变化。但在系统性红斑狼疮和类风湿关节炎患者中,正如我们在病例中观察到的,这种情况可能更频繁地出现。