Upregulation of endogenous intrahepatic interferon stimulated genes during chronic hepatitis C virus infection

被引:59
作者
MacQuillan, GC
Mamotte, C
Reed, WD
Jeffrey, GP
Allan, JE
机构
[1] Univ Western Australia, Dept Med, Nedlands, WA 6009, Australia
[2] Sir Charles Gairdner Hosp, Dept Gastroenterol & Hepatol, Nedlands, WA 6009, Australia
[3] Royal Perth Hosp, Dept Clin Immunol & Biochem Genet, Perth, WA, Australia
[4] Hollywood Private Hosp, Nedlands, WA, Australia
关键词
MxA; PKR; oligoadenylate synthetase; ISG15; interleukin; 8; NONSTRUCTURAL 5A PROTEIN; BLOOD MONONUCLEAR-CELLS; MESSENGER-RNA; KINASE PKR; INITIAL TREATMENT; RANDOMIZED TRIAL; REGULATED GENES; PLUS RIBAVIRIN; I INTERFERONS; MX GENES;
D O I
10.1002/jmv.10381
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The success of interferon-alpha and ribavirin combination therapy for the treatmeht of chronic hepatitis C viral infection differs between patients. In an attempt to identify predictors of host response to therapy, the levels of mRNA for interferon (IFN) stimulated genes: MxA, PKR, 2'5' OAS, ISG15, and interleukin 8 (IL-8), were examined in liver by real-time RT-PCR prior to commencement of therapy, The levels of intrahepatic classical IFN stimulated genes, but not IL-8, in chronic HCV disease (n=44) were found to be significantly upregulated (P<0.001) compared to the control cohort (n=12). The genotype of the infecting HCV strain did not influence IFN stimulated gene expression. These results suggest that the endogenous type 1 IFN antiviral effector pathway is broadly activated during chronic HCV disease, although the levels of mRNA for any of the IFN-stimulated genes tested did not predict the outcome of combination therapy.
引用
收藏
页码:219 / 227
页数:9
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