Immunity, Cancer & Stem Cells Group, Department of Biochemistry and Molecular and Cell Biology, Faculty of Sciences, Campus San Francisco Sq., University of Zaragoza and Aragón Health Research Institute (IIS Aragón), E-50009 Zaragoza, Spain.
Department of Biochemistry and Molecular and Cell Biology, Faculty of Sciences, Campus San Francisco Sq., University of Zaragoza and Aragón Health Research Institute (IIS Aragón), E-50009 Zaragoza, Spain.
Cells. 2019 Feb 12;8(2):154. doi: 10.3390/cells8020154.
T-cell mediated immune responses should be regulated to avoid the development of autoimmune or chronic inflammatory diseases. Several mechanisms have been described to regulate this process, namely death of overactivated T cells by cytokine deprivation, suppression by T regulatory cells (Treg), induction of expression of immune checkpoint molecules such as CTLA-4 and PD-1, or activation-induced cell death (AICD). In addition, activated T cells release membrane microvesicles called exosomes during these regulatory processes. In this review, we revise the role of exosome secretion in the different pathways of immune regulation described to date and its importance in the prevention or development of autoimmune disease. The expression of membrane-bound death ligands on the surface of exosomes during AICD or the more recently described transfer of miRNA or even DNA inside T-cell exosomes is a molecular mechanism that will be analyzed.
T 细胞介导的免疫应答应受到调节,以避免自身免疫或慢性炎症性疾病的发展。已经描述了几种调节此过程的机制,即通过细胞因子剥夺导致过度激活的 T 细胞死亡、T 调节细胞(Treg)的抑制、表达免疫检查点分子如 CTLA-4 和 PD-1 的诱导,或激活诱导的细胞死亡(AICD)。此外,在这些调节过程中,激活的 T 细胞释放称为外泌体的膜微泡。在这篇综述中,我们回顾了外泌体分泌在迄今为止描述的不同免疫调节途径中的作用及其在预防或发展自身免疫性疾病中的重要性。在 AICD 过程中外泌体表面表达膜结合的死亡配体,或最近描述的 miRNA 甚至 DNA 在内体 T 细胞外泌体中的转移,是一种分子机制,将对其进行分析。