Mallone Roberto, Brezar Vedran, Boitard Christian
INSERM, U986, Hôpital St Vincent de Paul, 82 avenue Denfert Rochereau, 75014 Paris, France.
Clin Dev Immunol. 2011;2011:513210. doi: 10.1155/2011/513210. Epub 2011 Jul 19.
Type 1 diabetes (T1D) is an autoimmune disease driven by the activation of lymphocytes against pancreatic β-cells. Among β-cell autoantigens, preproinsulin has been ascribed a key role in the T1D process. The successive steps that control the activation of autoreactive lymphocytes have been extensively studied in animal models of T1D, but remains ill defined in man. In man, T lymphocytes, especially CD8(+) T cells, are predominant within insulitis. Developing T-cell assays in diabetes autoimmunity is, thus, a major challenge. It is expected to help defining autoantigens and epitopes that drive the disease process, to pinpoint key functional features of epitope-specific T lymphocytes along the natural history of diabetes and to pave the way towards therapeutic strategies to induce immune tolerance to β-cells. New T-cell technologies will allow defining autoreactive T-cell differentiation programs and characterizing autoimmune responses in comparison with physiologically appropriate immune responses. This may prove instrumental in the discovery of immune correlates of efficacy in clinical trials.
1型糖尿病(T1D)是一种自身免疫性疾病,由淋巴细胞针对胰腺β细胞的激活所驱动。在β细胞自身抗原中,胰岛素原前体在T1D发病过程中被认为起着关键作用。在T1D动物模型中,对控制自身反应性淋巴细胞激活的连续步骤进行了广泛研究,但在人类中仍不清楚。在人类中,T淋巴细胞,尤其是CD8(+) T细胞,在胰岛炎中占主导地位。因此,开发糖尿病自身免疫中的T细胞检测方法是一项重大挑战。预计这将有助于确定驱动疾病进程的自身抗原和表位,确定表位特异性T淋巴细胞在糖尿病自然病程中的关键功能特征,并为诱导对β细胞免疫耐受的治疗策略铺平道路。新的T细胞技术将能够确定自身反应性T细胞分化程序,并与生理上适当的免疫反应相比,对自身免疫反应进行特征描述。这可能在临床试验中发现疗效的免疫相关因素方面发挥重要作用。