Barbara Davis Center for Diabetes, Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Immunol Rev. 2022 Mar;306(1):181-199. doi: 10.1111/imr.13043. Epub 2021 Nov 25.
Autoimmunity arises when mechanisms of immune tolerance fail. Here we discuss mechanisms of T cell activation and tolerance and the dynamics of the autoimmune response at the site of disease. Live imaging of autoimmunity provides the ability to analyze immune cell dynamics at the single-cell level within the complex intact environment where disease occurs. These analyses have revealed mechanisms of T cell activation and tolerance in the lymph nodes, mechanisms of T cell entry into sites of autoimmune disease, and mechanisms leading to pathogenesis or protection in the autoimmune lesions. The overarching conclusions point to stable versus transient T cell antigen presenting cell interactions dictating the balance between T cell activation and tolerance, and T cell restimulation as a driver of pathogenesis at the site of autoimmunity. Findings from models of multiple sclerosis and type 1 diabetes are highlighted, however, the results have implications for basic mechanisms of T cell regulation during immune responses, tumor immunity, and autoimmunity.
当免疫耐受机制失效时,自身免疫就会出现。在这里,我们讨论 T 细胞激活和耐受的机制,以及疾病部位自身免疫反应的动态。自身免疫的实时成像提供了在发生疾病的复杂完整环境中,以单细胞水平分析免疫细胞动态的能力。这些分析揭示了淋巴结中 T 细胞激活和耐受的机制、T 细胞进入自身免疫性疾病部位的机制,以及导致自身免疫病变中发病机制或保护的机制。总体结论表明,稳定的与短暂的 T 细胞抗原呈递细胞相互作用决定了 T 细胞激活和耐受之间的平衡,而 T 细胞再刺激是自身免疫部位发病机制的驱动因素。突出了多发性硬化症和 1 型糖尿病模型的研究结果,但这些结果对免疫反应、肿瘤免疫和自身免疫过程中 T 细胞调节的基本机制具有重要意义。