School of First Clinical Medicine, Heilongjiang University of Chinese Medicine, Harbin, China.
Department of Liver, Spleen and Stomach Diseases, First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, China.
Front Immunol. 2023 Mar 8;14:1150879. doi: 10.3389/fimmu.2023.1150879. eCollection 2023.
Autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), and IgG4-related sclerosing cholangitis (IgG4-SC) are the four main forms of autoimmune liver diseases (AILDs), which are all defined by an aberrant immune system attack on the liver. Most previous studies have shown that apoptosis and necrosis are the two major modes of hepatocyte death in AILDs. Recent studies have reported that inflammasome-mediated pyroptosis is critical for the inflammatory response and severity of liver injury in AILDs. This review summarizes our present understanding of inflammasome activation and function, as well as the connections among inflammasomes, pyroptosis, and AILDs, thus highlighting the shared features across the four disease models and gaps in our knowledge. In addition, we summarize the correlation among NLRP3 inflammasome activation in the liver-gut axis, liver injury, and intestinal barrier disruption in PBC and PSC. We summarize the differences in microbial and metabolic characteristics between PSC and IgG4-SC, and highlight the uniqueness of IgG4-SC. We explore the different roles of NLRP3 in acute and chronic cholestatic liver injury, as well as the complex and controversial crosstalk between various types of cell death in AILDs. We also discuss the most up-to-date developments in inflammasome- and pyroptosis-targeted medicines for autoimmune liver disorders.
自身免疫性肝炎 (AIH)、原发性胆汁性胆管炎 (PBC)、原发性硬化性胆管炎 (PSC) 和 IgG4 相关硬化性胆管炎 (IgG4-SC) 是四种主要的自身免疫性肝病 (AILD),其均由免疫系统异常攻击肝脏引起。大多数先前的研究表明,细胞凋亡和坏死是 AILD 中肝细胞死亡的两种主要模式。最近的研究报告称,炎性小体介导的细胞焦亡对于 AILD 中的炎症反应和肝损伤的严重程度至关重要。本综述总结了我们目前对炎性小体激活和功能的认识,以及炎性小体、细胞焦亡和 AILD 之间的联系,从而突出了这四种疾病模型的共同特征和我们知识上的空白。此外,我们总结了 PBC 和 PSC 中肝脏-肠道轴、肝损伤和肠道屏障破坏之间 NLRP3 炎性小体激活的相关性。我们总结了 PSC 和 IgG4-SC 之间微生物和代谢特征的差异,并强调了 IgG4-SC 的独特性。我们探讨了 NLRP3 在急性和慢性胆汁淤积性肝损伤中的不同作用,以及 AILD 中各种类型细胞死亡之间复杂且有争议的相互作用。我们还讨论了针对自身免疫性肝病的炎性小体和细胞焦亡靶向药物的最新进展。