Department of Endocrinology & Diabetes, Università Campus Bio-Medico, Via Álvaro del Portillo 21 - 00128, Rome, Italy.
Curr Pharm Des. 2011;17(29):3224-8. doi: 10.2174/138161211798157531.
In type 1 diabetes, beta cells are attacked and destroyed by auto reactive T cells causing major impairment of blood glucose metabolism and, ultimately, the development of life-threatening complications. Currently, the treatment of this chronic disease is based on the use of endogenous insulin and no curative therapies are available. Treatment approaches in this respect need to be directed toward the primary causes of the disease tackling beta cells' auto reactive T cells. The goal of any curative intervention in type 1 diabetes is the preservation of insulin-secreting cells. This may be achieved by the abrogation of the pathogenic reactivity to beta cell auto antigens while preserving full capacity to generate a normal immune response against foreign antigens. In this review, some of the most promising drugs for immune intervention in type 1 diabetes are presented and discussed including phase 3 clinical trials that involve: DiaPep277, Anti-CD3 Otelixizumab, Glutamic Acid Decarboxylase (GAD) and anti-IL1 receptor antagonist. These approaches are currently being tested in international multicenter trials and all of them have a very similar outcome in terms of a beneficial effect on beta cells.
在 1 型糖尿病中,β细胞被自身反应性 T 细胞攻击和破坏,导致血糖代谢严重受损,最终发展为危及生命的并发症。目前,这种慢性疾病的治疗基于内源性胰岛素的使用,尚无治愈疗法。在这方面,治疗方法需要针对疾病的主要原因,即针对β细胞自身反应性 T 细胞。任何 1 型糖尿病的治愈干预的目标都是保护胰岛素分泌细胞。这可以通过消除对β细胞自身抗原的致病反应来实现,同时保持对外国抗原产生正常免疫反应的全部能力。在这篇综述中,介绍并讨论了一些用于 1 型糖尿病免疫干预的最有前途的药物,包括涉及 DiaPep277、抗-CD3 Otelixizumab、谷氨酸脱羧酶 (GAD) 和抗-IL1 受体拮抗剂的 3 期临床试验。这些方法目前正在国际多中心试验中进行测试,它们在对β细胞的有益影响方面都具有非常相似的结果。