Hehmke B, Michaelis D, Hildmann W, Richter K V, Kohnert K D
Central Institute of Diabetes Gerhardt Katsch, Karlsburg, GDR.
Exp Clin Endocrinol. 1987 Aug;89(3):375-82. doi: 10.1055/s-0029-1210665.
Serum activities of complement-dependent antibody mediated cytotoxicity (C'AMC) were determined in 36 consecutive patients with newly diagnosed insulin-dependent diabetes mellitus (IDDM). The sequential exposure of 51Cr labeled neonatal rat islet cells to patient serum and rabbit complement revealed the presence of C'AMC in 28 IDDM subjects. The C'AMC titres ranged between 1:4 and 1:512 and were not related to the C'AMC activity of a given sample as measured at a standard dilution (1:4). In comparison to the clinical characteristics of 21 IDDM patients with negative C'AMC, higher C'AMC titres (greater than or equal to 1:32) were associated with a lower mean age at diagnosis of IDDM (12.2 +/- 2.1 vs. 19.0 +/- 2.3 years; p less than 0.05), with a higher frequency of infections up to 6 months prior to diagnosis (6 out of 11 vs. 3 out of 21 patients; p less than 0.05) and, although statistically not significant, a preponderance of female sex together with a decreased frequency of HLA-DR4. In contrast, fasting C-peptides levels, HLA-DR3 antigen frequency and Coxsackie B1-6 virus antibody titres were not related to the C'AMC titres. It is concluded that (1) C'AMC titration is superior to the detection of initial C'AMC levels for evaluating the strength of the complement-dependent humoral immune response towards islet cell surface (auto)antigen(s), and (2) infectious agents may be involved in eliciting a C'AMC response.
对36例新诊断的胰岛素依赖型糖尿病(IDDM)患者连续测定了补体依赖抗体介导的细胞毒性(C'AMC)的血清活性。将51Cr标记的新生大鼠胰岛细胞依次暴露于患者血清和兔补体后,发现28例IDDM患者存在C'AMC。C'AMC滴度在1:4至1:512之间,与在标准稀释度(1:4)下测得的给定样本的C'AMC活性无关。与21例C'AMC阴性的IDDM患者的临床特征相比,较高的C'AMC滴度(大于或等于1:32)与IDDM诊断时的较低平均年龄相关(12.2±2.1岁对19.0±2.3岁;p<0.05),与诊断前6个月内较高的感染频率相关(11例中有6例对21例中有3例;p<0.05),并且尽管在统计学上不显著,但女性占优势且HLA-DR4频率降低。相比之下,空腹C肽水平、HLA-DR3抗原频率和柯萨奇B1-6病毒抗体滴度与C'AMC滴度无关。得出的结论是:(1)对于评估针对胰岛细胞表面(自身)抗原的补体依赖体液免疫反应的强度,C'AMC滴定优于初始C'AMC水平的检测;(2)感染因子可能参与引发C'AMC反应。