非胰岛素依赖型糖尿病患者的循环免疫复合物和外周血B淋巴细胞。

Acta physiologica latino americana Pub Date : 1983-01-01
R I Barañao, P A Tesone, N A Chasseing, M Mendelson, L S Rumi
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引用次数: 0

摘要

对27例非胰岛素依赖型糖尿病(NIDD)患者进行血清循环免疫复合物(CIC)测定。这是通过测量C3b补体部分与人类红细胞的结合程度来完成的。同时,采用直接免疫荧光法检测外周血B淋巴细胞的百分率,检测具有C3b补体部分受体的细胞表面IgG和EAC花环。同时对20名正常对照者采用相同的方法进行研究。与健康受试者相比,NIDD患者血清CIC升高。值分别为35.8 +/- 3.2和25.6 +/- 2.1微克/毫升。糖尿病患者表面IgG细胞比例为10.2 +/- 0.8;这一数值显著高于对照组(6.0 +/- 0.8)。NIDD患者与对照组之间EAC结合细胞百分比的定量差异无统计学意义。将NIDD患者分为有微血管并发症组和无微血管并发症组两组时,CIC水平和B淋巴细胞百分比均无差异。最高CIC水平与最高表面IgG淋巴细胞百分比之间没有任何相关性。这些数据表明,在未接受胰岛素治疗的NIDD患者中,CIC水平和表面IgG细胞增加,至少不是在持续或长期治疗中。这可能使我们怀疑存在不同于胰岛素依赖型糖尿病中发现的胰岛素-抗胰岛素CIC的抗原-抗体复合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating immune complexes and peripheral B lymphocytes in non insulin dependent diabetic patients.

Serum circulating immune complexes (CIC) were measured in 27 patients with non insulin dependent diabetes (NIDD). This was done by measuring the degree of binding to human red blood cells by the C3b complement fraction. At the same time, the percentage of B lymphocytes in peripheral blood was evaluated by means of the direct immunofluorescence technique for surface IgG and EAC rosettes for cells with receptors to C3b complement fraction. Twenty normal control subjects were simultaneously studied by the same methodology. An increase in serum CIC was observed in NIDD patients, as compared to healthy subjects. Values were 35.8 +/- 3.2 and 25.6 +/- 2.1 micrograms/ml, respectively. The percentage of cells with surface IgG was 10.2 +/- 0.8 in diabetic patients; this value was significantly higher than that found in the control group (6.0 +/- 0.8). No significant quantitative difference in the percentage of EAC binding cells was found between NIDD patients and the control group. When NIDD patients were divided into two groups, those with and those without microvascular complications, neither differences in CIC levels nor in the percentage of B lymphocytes were found. Nor any correlation could be found between the highest individual CIC levels and the highest percentage of lymphocytes with surface IgG. These data show an increase of CIC levels and of cells with surface IgG in NIDD patients who had not received insulin at least not in a constant or prolonged therapy. This could allow us to suspect the existence of antigen-antibody complexes different to insulin-antiinsulin CIC found in insulin dependent diabetes.

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