Serum IP-10 Levels Correlate with the Severity of Liver Histopathology in Patients Infected with Genotype-1 HCV
0
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Background/Aims: Interferon-γ-inducible protein 10 (IP-10)plays important roles in the pathogenesis of hepatitis C virus (HCV) infection. We investigated the association between serum IP-10 levels and liver pathology in patients with chronic HCV infection. Methods: The serum IP-10 concentration was assessed in 85 patients with chronic HCV infection using a solid phase sandwich enzyme-linked immunosorbent assay,and a liver biopsy specimen was obtained. The pathology was scored using the Knodell histologic activity index (HAI). Results: Of the 85 patients, 58 had genotype 1 HCV infection,21 had genotype non-1, and 6 were undetermined. The serum IP-10 levels did not differ between patients infected with genotype 1 and genotype non-1 (p=0.472). In patients with genotype 1 infection, the total HAI score and the stage of fi brosis were highly correlated with the serum IP-10 level (r=0.555, r=0.578, p<0.001). Furthermore, the serum IP-10concentrations of patients with severe fi brosis (stages 3, 4)were higher than those of patients with mild fi brosis (stages 0 to 2; 214.4 vs. 72.3 pg/mL, p=0.002) among patients with genotype 1 infection. However, in patients without genotype 1 infection, the histopathology was not associated with the serum IP-10 level. A multivariate analysis showed that serum IP-10 was an independent predictor of fi brosis (stages 3, 4)in patients with genotype 1 infection (odds ratio, 1.034; 95%confi dence interval, 1.006 to 1.064; p=0.018). Conclusions:Serum IP-10 concentration was signifi cantly correlated with the severity of liver histology in genotype 1 HCV infection.
Abstract
Background/Aims: Interferon-γ-inducible protein 10 (IP-10)plays important roles in the pathogenesis of hepatitis C virus (HCV) infection. We investigated the association between serum IP-10 levels and liver pathology in patients with chronic HCV infection. Methods: The serum IP-10 concentration was assessed in 85 patients with chronic HCV infection using a solid phase sandwich enzyme-linked immunosorbent assay,and a liver biopsy specimen was obtained. The pathology was scored using the Knodell histologic activity index (HAI). Results: Of the 85 patients, 58 had genotype 1 HCV infection,21 had genotype non-1, and 6 were undetermined. The serum IP-10 levels did not differ between patients infected with genotype 1 and genotype non-1 (p=0.472). In patients with genotype 1 infection, the total HAI score and the stage of fi brosis were highly correlated with the serum IP-10 level (r=0.555, r=0.578, p<0.001). Furthermore, the serum IP-10concentrations of patients with severe fi brosis (stages 3, 4)were higher than those of patients with mild fi brosis (stages 0 to 2; 214.4 vs. 72.3 pg/mL, p=0.002) among patients with genotype 1 infection. However, in patients without genotype 1 infection, the histopathology was not associated with the serum IP-10 level. A multivariate analysis showed that serum IP-10 was an independent predictor of fi brosis (stages 3, 4)in patients with genotype 1 infection (odds ratio, 1.034; 95%confi dence interval, 1.006 to 1.064; p=0.018). Conclusions:Serum IP-10 concentration was signifi cantly correlated with the severity of liver histology in genotype 1 HCV infection.
참고문헌 (28)
- Ferrari C, "Immunopathogenesis of hepatitis C virus infection", J Hepatol, 31(Suppl 1), pp.31~38 (1999)
- Chazouilleres O, "Quantitation of hepatitis C virus RNA in liver transplant recipients", Gastroenterology, 106, pp.994~999 (1994)
- Fong TL, "Short-term prednisone therapy affects aminotransferase activity and hepatitis C virus RNA levels in chronic hepatitis C", Gastroenterology, 107, pp.196~199 (1994)
- Wald O, "Chemokines in hepatitis C virus infection: pathogenesis, prognosis and therapeutics", Cytokine, 39, pp.50~62 (2007)
- Zeremski M, "The role of chemokines as inflammatory mediators in chronic hepatitis C virus infection", J Viral Hepat, 14, pp.675~687 (2007)
- Qin S, "The chemokine receptors CXCR3 and CCR5 mark subsets of T cells associated with certain inflammatory reactions", J Clin Invest, 101, pp.746~754 (1998)
- Bonecchi R, "Differential expression of chemokine receptors and chemotactic responsiveness of type 1 T helper cells (Th1s) and Th2s", J Exp Med, 187, pp.129~134 (1998)
- Loetscher P, "CCR5 is characteristic of Th1 lymphocytes", Nature, 391, pp.344~345 (1998)
- Asselah T, "Liver gene expression signature of mild fibrosis in patients with chronic hepatitis C", Gastroenterology, 129, pp.2064~2075 (2005)
- Bièche I, "Molecular profiling of early stage liver fibrosis in patients with chronic hepatitis C virus infection", Virology, 332, pp.130~144 (2005)
- Shields PL, "Chemokine and chemokine receptor interactions provide a mechanism for selective T cell recruitment to specific liver compartments within hepatitis C-infected liver", J Immunol, 163, pp.6236~6243 (1993)
- Springer TA, "Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm", Cell, 76, pp.301~314 (1994)
- Lalor PF, "Recruitment of lymphocytes to the human liver", Immunol Cell Biol, 85, pp.52~64 (2002)
- Taub DD, "Recombinant human interferon-inducible protein 10 is a chemoattractant for human monocytes and T lymphocytes and promotes T cell adhesion to endothelial cells", J Exp Med, 177, pp.1809~1814 (1993)
- Taub DD, "Alpha and beta chemokines induce NK cell migration and enhance NK-mediated cytolysis", J Immunol, 155, pp.3877~3888 (1995)
- Patzwahl R, "Enhanced expression of interferon-regulated genes in the liver of patients with chronic hepatitis C virus infection: detection by suppression-subtractive hybridization", J Virol, 75, pp.1332~1338 (2001)
- Mihm S, "Expression of the chemokine IP-10 correlates with the accumulation of hepatic IFN-gamma and IL-18 mRNA in chronic hepatitis C but not in hepatitis B", J Med Virol, 70, pp.562~570 (2003)
- Neville LF, "The immunobiology of interferon- gamma inducible protein 10 kD (IP-10): a novel, pleiotropic member of the C-X-C chemokine superfamily", Cytokine Growth Factor Rev, 8, pp.207~219 (1997)
- Narumi S, "Expression of IFN-inducible protein-10 in chronic hepatitis", J Immunol, 158, pp.5536~5544 (1997)
- Bertoletti A, "Different cytokine profiles of intraphepatic T cells in chronic hepatitis B and hepatitis C virus infections", Gastroenterology, 112, pp.193~199 (1997)
- Khakoo SI, "Lymphocyte and macrophage phenotypes in chronic hepatitis C infection. Correlation with disease activity", Am J Pathol, 150, pp.963~970 (1997)
- Mihm S, "Hepatic expression of inducible nitric oxide synthase transcripts in chronic hepatitis C virus infection: relation to hepatic viral load and liver injury", Hepatology, 26, pp.451~458 (1997)
- Mihm S, "High inflammatory activity is associated with an increased amount of IFN-gamma transcripts in peripheral blood cells of patients with chronic hepatitis C virus infection", Med Microbiol Immunol, 185, pp.95~102 (1996)
- Mochizuki K, "B7", BB-1 expression and hepatitis activity in liver tissues of patients with chronic hepatitis C, 1997, pp.25, 713~718
- Hua LL, "Distinct patterns of stimulus-inducible chemokine mRNA accumulation in human fetal astrocytes and microglia", Glia, 30, pp.74~81 (2000)
- Harvey CE, "Expression of the chemokine IP-10 (CXCL10) by hepatocytes in chronic hepatitis C virus infection correlates with histological severity and lobular inflammation", J Leukoc Biol, 74, pp.360~369 (2003)
- Diago M, "Association of pretreatment serum interferon gamma inducible protein 10 levels with sustained virological response to peginterferon plus ribavirin therapy in genotype 1 infected patients with chronic hepatitis C", Gut, 55, pp.374~379 (2006)
- Romero AI, "Interferon (IFN)-gammainducible protein-10: association with histological results, viral kinetics, and outcome during treatment with pegylated IFN-alpha 2a and ribavirin for chronic hepatitis C virus infection", J Infect Dis, 194, pp.895~903 (2006)
