炎症小体在慢性病毒性肝炎中的作用

Pin Wan, Ge Yang, Qi Cheng, Xuelong Zhang, Zhaoyang Yue, Moran Li, Chunlin Liu, Qian Yi, Yaling Jia, Jinbiao Liu, Xiwen Xing, Binlian Sun, Yongkui Li
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引用次数: 0

摘要

致肝病毒感染会导致一系列肝脏疾病,包括急性肝炎、慢性肝炎以及随之而来的肝硬化和肝细胞癌(HCC)。在五种典型的致肝病毒中,乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)通常会持续感染人类并引发慢性肝炎,给人类带来巨大的困扰。以往的研究表明,多种类型的炎性体参与了 HBV 和 HCV 的感染。NLRP3 炎症小体可被 HBV 和 HCV 激活和调控。根据不同的实验模型,它可在病毒感染中发挥抗病毒功能或介导炎症反应。除了 NLRP3 炎症小体,IFI16 和 AIM2 炎症小体也参与了乙型肝炎的病理过程,NALP3 炎症小体可感知肝细胞中的 HCV 感染。炎性体通过其下游分泌炎性细胞因子白细胞介素-1β(IL-1β)和 IL-18,或通过裂解的气体蛋白 D(GSDMD)诱导热蛋白沉积,影响病毒性肝炎的病理过程。然而,炎性体在病毒感染不同阶段的作用仍不明确。今后应开发更多适当的病毒性肝炎实验模型进行具体研究,以便我们能更深入地了解炎性体调控的复杂性以及炎性体及其下游效应物在 HBV 和 HCV 感染过程中的多重功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of inflammasome in chronic viral hepatitis
Infections of hepatotropic viruses cause a wide array of liver diseases including acute hepatitis, chronic hepatitis and the consequently developed cirrhosis and hepatocellular carcinoma (HCC). Among the five classical hepatotropic viruses, hepatitis B virus (HBV) and hepatitis C virus (HCV) usually infect human persistently and cause chronic hepatitis, leading to major troubles to humanity. Previous studies have revealed that several types of inflammasomes are involved in the infections of HBV and HCV. Here, we summarize the current knowledge about their roles in hepatitis B and C. NLRP3 inflammasome can be activated and regulated by HBV and HCV. It is found to exert antiviral function or mediates inflammatory response in viral infections depending on different experimental models. Besides NLRP3 inflammasome, IFI16 and AIM2 inflammasomes participate in the pathological process of hepatitis B, and NALP3 inflammasome may sense HCV infection in hepatocytes. The inflammasomes affect the pathological process of viral hepatitis through its downstream secretion of inflammatory cytokines interleukin-1β (IL-1β) and IL-18 or induction of pyroptosis resulting from cleaved gasdermin D (GSDMD). However, the roles of inflammasomes in different stages of viral infection remains mainly unclear. More proper experimental models of viral hepatitis should be developed for specific studies in future, so that we can understand more about the complexity of inflammasome regulation and multifunction of inflammasomes and their downstream effectors during HBV and HCV infections.
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