Institute of Diabetes Research, Group Immune Tolerance Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum München, Heidemannstrasse 1, 80939 Munich, Germany; Deutsches Zentrum für Diabetesforschung (DZD), Ingolstaedter Landstrasse 1, 85764 Munich-Neuherberg, Germany.
Islet Biology Group (IBEx), Exeter Centre of Excellence in Diabetes (EXCEED), University of Exeter College of Medicine and Health, Exeter EX2 5DW, UK.
Mol Metab. 2022 Oct;64:101565. doi: 10.1016/j.molmet.2022.101565. Epub 2022 Aug 6.
The highly complex pathogenesis of Type 1 Diabetes is driven by several immune cell types with both effector and regulatory characteristics, which ultimately ends in the destruction of the insulin-producing beta cells. There are multiple layers of interaction between these immune cell populations and the pancreatic islets.
In this review article, we aim to discuss important recent insights into the multiple layers of interaction between immune cell populations and the pancreatic islets. Specifically, we discuss the environment where immune and beta cell interactions occur, the key cell types and molecules involved, and the outcomes of these interactions.
Most of the molecular mechanisms underlying aberrant immune cell activation and impaired immune tolerance remain insufficiently understood, which hinders the development of efficient prevention and treatment strategies. In order to overcome this knowledge gap, a better understanding of the complex interactions of immune cells and beta cells, including both the underlying protective and pathogenic mechanisms is urgently required.
1 型糖尿病的发病机制非常复杂,涉及多种具有效应和调节特性的免疫细胞,最终导致胰岛素分泌细胞β的破坏。这些免疫细胞群与胰岛之间存在着多层次的相互作用。
在这篇综述文章中,我们旨在讨论免疫细胞群与胰岛之间相互作用的多个层面的重要最新见解。具体而言,我们讨论了免疫细胞和β细胞相互作用发生的环境、涉及的关键细胞类型和分子,以及这些相互作用的结果。
大多数导致异常免疫细胞激活和免疫耐受受损的分子机制仍了解不足,这阻碍了有效预防和治疗策略的发展。为了克服这一知识差距,迫切需要更好地了解免疫细胞和β细胞的复杂相互作用,包括潜在的保护和致病机制。