Eisenbarth G S, Jackson R A, Pugliese A
Section of Immunology & Immunogenetics, Joslin Diabetes Center, Harvard Medical School, Massachusetts.
J Autoimmun. 1992 Apr;5 Suppl A:241-6. doi: 10.1016/0896-8411(92)90039-s.
Type I diabetes is preceded by a series of autoantibodies including recently recognized subtypes of cytoplasmic islet cell antibodies (ICA) which we have termed 'restricted' and 'non-restricted'. Amongst the autoantibodies detected in prediabetics the antibodies to insulin are unique in that their levels correlate with the rate of progression to type I diabetes. The levels of insulin autoantibodies appear to be stably regulated prior to the appearance of ICA and the highest levels are associated with expression of DR4. The above studies have led to the hypothesis that an immune response to insulin is an early and central feature of anti-islet autoimmunity and that such as immune response when associated with loss of tolerance to other islet antigens (e.g. ICA) is pathogenic.
1型糖尿病之前会出现一系列自身抗体,包括最近发现的细胞质胰岛细胞抗体(ICA)的亚型,我们将其称为“限制性”和“非限制性”。在糖尿病前期患者检测到的自身抗体中,胰岛素抗体很独特,因为其水平与进展为1型糖尿病的速率相关。在ICA出现之前,胰岛素自身抗体水平似乎受到稳定调节,且最高水平与DR4的表达相关。上述研究得出一个假说,即针对胰岛素的免疫反应是抗胰岛自身免疫的早期核心特征,并且当这种免疫反应与对其他胰岛抗原(如ICA)的耐受性丧失相关时,具有致病性。