Schildgen O, Fiedler M, Dahmen U, Li J, Lohrengel B, Lu M, Roggendorf M
University Hospital Essen, Institute of Virology, Hufelandstrasse 55, D-45122 Essen, Germany.
Immunol Lett. 2006 Jan 15;102(1):31-7. doi: 10.1016/j.imlet.2005.06.007. Epub 2005 Jul 14.
The woodchuck together with the woodchuck hepatitis virus (WHV) is an excellent model to study the pathogenesis of hepadnaviral infections. Chronic WHV infection causes severe liver disease and hepatocellular carcinoma in woodchucks. The mechanism of viral clearance is not fully understood, interferons seem to play a major role in down-regulating viral replication prior to elimination of infected hepatocytes. We investigated on the pattern of cytokine and T-cell-marker expression in livers of woodchucks chronically infected with WHV. RNase-protection-assay (RPA) was used to determine mRNA of woodchuck specific genes (TNF-alpha, IFN-gamma, IL-15, CD3, CD4, CD8). Serial liver biopsies were performed daily or weekly in eight chronic WHV-carrier woodchucks. Cytokine/T-cell-marker expression differed significantly between the time points up to +/-50% within each woodchuck. The different expression patterns of cytokines or T-cell-markers did not correlate to the (weak) fluctuations in the viremia but may explain the observed fluctuations in the WHV/HBV-load in chronically infected individuals. Furthermore, we observed associations between cytokine and T-cell-marker expression. The marginal fluctuations in viremia during the chronic infection may indicate, that, once the chronic hepadnaviral infection is established, cytokines/interferons expressed endogenously (i.e. not vector-borne or injected) play only a minor role.
土拨鼠与土拨鼠肝炎病毒(WHV)是研究嗜肝DNA病毒感染发病机制的优秀模型。慢性WHV感染可导致土拨鼠出现严重肝病和肝细胞癌。病毒清除机制尚未完全明确,干扰素似乎在清除受感染肝细胞之前下调病毒复制过程中发挥主要作用。我们研究了慢性感染WHV的土拨鼠肝脏中细胞因子和T细胞标志物的表达模式。采用核糖核酸酶保护分析(RPA)来测定土拨鼠特异性基因(肿瘤坏死因子-α、干扰素-γ、白细胞介素-15、CD3、CD4、CD8)的mRNA。对8只慢性WHV携带土拨鼠每天或每周进行肝脏系列活检。在每只土拨鼠体内,各时间点之间细胞因子/T细胞标志物的表达差异显著,可达±50%。细胞因子或T细胞标志物的不同表达模式与病毒血症的(微弱)波动无关,但可能解释了慢性感染个体中观察到的WHV/HBV载量波动。此外,我们还观察到细胞因子与T细胞标志物表达之间的关联。慢性感染期间病毒血症的微小波动可能表明,一旦建立慢性嗜肝DNA病毒感染,内源性表达(即非载体携带或注射)的细胞因子/干扰素仅起次要作用。