Giannelli G, Antonaci S
Department of Internal Medicine, Immunology, and Infectious Diseases, Section of Internal Medicine, University of Bari Medical School, Cesare Frugoni Medical Clinic, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Histol Histopathol. 2005 Jul;20(3):939-44. doi: 10.14670/HH-20.939.
Chronic C hepatitis represents a major health problem worldwide, mainly because progression of the tissue damage leads to the development of cirrhosis and hepatocellular carcinoma. In this review we discuss the molecular mechanisms underlying the development of liver fibrosis. In particular we consider some immunologic aspects that regulate the interaction between HCV and the host immune defense. Reflections are made about the roles played by the host capacity to respond to the viral infection during therapy and the consequences of the deposition of extracellular matrix (ECM) proteins leading to the development of fibrosis. The involvement of inflammatory cytokines in regulating the proteolytic remodeling of the liver and the ECM turn-over is essential for the activation of hepatic stellate cells (HSCs), that have an important role in the progression of liver fibrosis. Finally, we analyze one of the aspects involved in the activation of the HSCs, namely the proteolytic remodeling of the surrounding environment.
慢性丙型肝炎是全球主要的健康问题,主要原因是组织损伤的进展会导致肝硬化和肝细胞癌的发生。在本综述中,我们讨论了肝纤维化发生的分子机制。特别地,我们考虑了一些调节丙型肝炎病毒(HCV)与宿主免疫防御之间相互作用的免疫学方面。对宿主在治疗期间对病毒感染的反应能力所起的作用以及细胞外基质(ECM)蛋白沉积导致纤维化发展的后果进行了思考。炎性细胞因子参与调节肝脏的蛋白水解重塑和ECM周转对于肝星状细胞(HSC)的激活至关重要,而肝星状细胞在肝纤维化进展中起重要作用。最后,我们分析了HSC激活所涉及的一个方面,即周围环境的蛋白水解重塑。