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非肥胖糖尿病易感性(NOD)小鼠的免疫紊乱与发病机制。

Immune disturbance and pathogenesis of non-obese diabetes-prone (NOD) mice.

作者信息

Harada M

机构信息

Shionogi Research Laboratories, Osaka, Japan.

出版信息

Exp Clin Endocrinol. 1987 Aug;89(3):251-8. doi: 10.1055/s-0029-1210647.

Abstract

Manipulation and possible mechanism of pathogenesis in NOD mice were studied from the immunological standpoint. Disturbance of lymphocyte activity, particularly that of T-lymphocyte activity, greatly influenced the development of overt diabetes. Throughout the test period when the mice were between 24 and 30 weeks old, spontaneous diabetes in female mice was markedly suppressed by treatment with anti-thymocyte serum or with an anti-Thy 1,2 monoclonal antibody. Also, the appearance of diabetes was promoted by cyclophosphamide treatment in animals of both sexes. Evidence for the role of T-lymphocytes was provided by the experiments using the T-lymphocyte-depleted mice. Neither insulitis nor overt diabetes was observed in the athymic nude congenic mice with the genetic background of NOD even if they were given cyclophosphamide. Insulitis was induced in the athymic nude recipients by the transfer of thymocytes or of splenocytes from euthymic littermates, although an overt diabetes was not produced by cell transfer alone. An overt diabetes was induced in the congenitally athymic nude mice by a single transfer of T-lymphocytes and subsequent treatment with cyclophosphamide. From these results it can be concluded that T-lymphocytes play an obligatory role in the pathogenesis of diabetes in NOD mice.

摘要

从免疫学角度研究了非肥胖糖尿病(NOD)小鼠的发病机制及可能的发病机理。淋巴细胞活性的紊乱,尤其是T淋巴细胞活性的紊乱,对显性糖尿病的发展有很大影响。在整个24至30周龄的测试期内,用抗胸腺细胞血清或抗Thy 1,2单克隆抗体治疗可明显抑制雌性小鼠的自发性糖尿病。此外,环磷酰胺治疗可促进两性动物糖尿病的出现。使用T淋巴细胞耗竭小鼠的实验为T淋巴细胞的作用提供了证据。即使给予环磷酰胺,具有NOD遗传背景的无胸腺裸基因小鼠也未观察到胰岛炎或显性糖尿病。通过从有胸腺的同窝仔鼠转移胸腺细胞或脾细胞,在无胸腺裸受体中诱导出胰岛炎,尽管单独的细胞转移并未产生显性糖尿病。通过单次转移T淋巴细胞并随后用环磷酰胺治疗,在先天性无胸腺裸小鼠中诱导出显性糖尿病。从这些结果可以得出结论,T淋巴细胞在NOD小鼠糖尿病的发病机制中起重要作用。

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