Center for Type 1 Diabetes Research, La Jolla Institute for Immunology, La Jolla, CA, USA.
The Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Institute of Diabetes Research, Munich-Neuherberg, Germany.
Sci Adv. 2020 Oct 16;6(42). doi: 10.1126/sciadv.abc5586. Print 2020 Oct.
Preproinsulin (PPI) is presumably a crucial islet autoantigen found in patients with type 1 diabetes (T1D) but is also recognized by CD8 T cells from healthy individuals. We quantified PPI-specific CD8 T cells within different areas of the human pancreas from nondiabetic controls, autoantibody-positive donors, and donors with T1D to investigate their role in diabetes development. This spatial cellular quantitation revealed unusually high frequencies of autoreactive CD8 T cells supporting the hypothesis that PPI is indeed a key autoantigen. To our surprise, PPI-specific CD8 T cells were already abundantly present in the nondiabetic pancreas, thus questioning the dogma that T1D is caused by defective thymic deletion or systemic immune dysregulation. During T1D development, these cells accumulated in and around islets, indicating that an islet-specific trigger such as up-regulation of major histocompatibility complex class I might be essential to unmask beta cells to the immune system.
前胰岛素原 (PPI) 据推测是 1 型糖尿病 (T1D) 患者中重要的胰岛自身抗原,但也被健康个体的 CD8 T 细胞识别。我们从非糖尿病对照者、自身抗体阳性供体和 T1D 供体的不同胰腺区域中定量了 PPI 特异性 CD8 T 细胞,以研究它们在糖尿病发展中的作用。这种空间细胞定量显示出异常高频率的自身反应性 CD8 T 细胞,支持 PPI 确实是关键自身抗原的假设。令我们惊讶的是,PPI 特异性 CD8 T 细胞在非糖尿病胰腺中已经大量存在,从而质疑 T1D 是由胸腺删除缺陷或全身免疫失调引起的观点。在 T1D 发展过程中,这些细胞在胰岛内外积聚,表明主要组织相容性复合体 I 类的上调等胰岛特异性触发可能是将β细胞暴露于免疫系统所必需的。