Bach Jean-François
INSERM U 25, Hôpital Necker, Paris, France.
Arthritis Res. 2002;4 Suppl 3(Suppl 3):S3-15. doi: 10.1186/ar554. Epub 2002 May 9.
The nonobese diabetic (NOD) mouse is a well-recognised animal model of spontaneous autoimmune insulin-dependent diabetes mellitus. The disease is T-cell mediated, involving both CD4 and CD8 cells. Its progress is controlled by a variety of regulatory T cells. An unprecedented number of immunological treatments have been assessed in this mouse strain. This chapter systematically reviews most of these therapeutic manoeuvres, discussing them in the context of their significance with regard to the underlying mechanisms and the potential clinical applications. The contrast between the surprisingly high rate of success found for a multitude of treatments (more than 160) administered early in the natural history of the disease and the few treatments active at a late stage is discussed in depth. Most of the concepts and strategies derived from this model apply to other autoimmune diseases, for which no such diversified data are available.
非肥胖型糖尿病(NOD)小鼠是一种公认的自发性自身免疫性胰岛素依赖型糖尿病动物模型。该疾病由T细胞介导,涉及CD4和CD8细胞。其进展受多种调节性T细胞控制。在这种小鼠品系中评估的免疫治疗方法数量空前。本章系统回顾了其中大部分治疗手段,并结合其在潜在机制和潜在临床应用方面的意义进行讨论。深入探讨了在疾病自然史早期给予多种治疗(超过160种)时惊人的高成功率与晚期少数有效治疗之间的对比。从该模型得出的大多数概念和策略适用于其他自身免疫性疾病,而对于这些疾病尚无如此多样化的数据。