Gremion Christel, Grabscheid Benno, Wölk Benno, Moradpour Darius, Reichen Jürg, Pichler Werner, Cerny Andreas
Clinic for Rheumatology and Clinical Immunology/Allergology, University of Bern, CH-3010 Bern, Switzerland.
J Virol. 2004 Feb;78(4):2152-7. doi: 10.1128/jvi.78.4.2152-2157.2004.
The role of Fas-mediated lysis of hepatocytes in hepatitis C virus (HCV)-induced injury is frequently discussed. We therefore analyzed the effect of the number of HCV antigen-expressing cells, the mode of antigen presentation, and the number of cytotoxic T lymphocytes in a coculture system mimicking cellular components of the liver. Here, we show that endogenously processed HCV proteins are capable of inducing bystander killing. We further demonstrate that 0.8 to 1.5% of cells presenting HCV antigens suffice to induce lysis of 10 to 29% of bystander cells, suggesting that the mechanism may be operative at low fractions of infected versus uninfected hepatocytes in vivo. Our data underscore the role of the Fas pathway in HCV-related liver injury and support the exploration of Fas-based treatment strategies for patients with chronic hepatitis C virus infection.
Fas介导的肝细胞裂解在丙型肝炎病毒(HCV)诱导的损伤中的作用常被讨论。因此,我们在模拟肝脏细胞成分的共培养系统中分析了HCV抗原表达细胞数量、抗原呈递方式和细胞毒性T淋巴细胞数量的影响。在此,我们表明内源性加工的HCV蛋白能够诱导旁观者杀伤。我们进一步证明,呈现HCV抗原的细胞中有0.8%至1.5%足以诱导10%至29%的旁观者细胞裂解,这表明该机制在体内感染与未感染肝细胞比例较低时可能起作用。我们的数据强调了Fas途径在HCV相关肝损伤中的作用,并支持探索基于Fas的治疗策略用于慢性丙型肝炎病毒感染患者。