ELISPOT analysis of hepatitis C virus protein-specific IFN-γ-producing peripheral blood lymphocytes in infected humans with and without cirrhosis

被引:34
作者
Anthony, DD [1 ]
Post, AB
Valdez, H
Peterson, DL
Murphy, M
Heeger, PS
机构
[1] Case Western Reserve Univ, Dept Med, Vet Affairs Med Ctr, Louis Stokes Cleveland Dept, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Univ Hosp Cleveland, Dept Med, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[4] Virginia Commonwealth Univ, Dept Biochem & Mol Biophys, Richmond, VA 23298 USA
关键词
T cell; cellular; immunity; cytokine; human; hepatitis C;
D O I
10.1006/clim.2001.5018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An improved ability to monitor hepatitis C virus (HCV)-specific T cell immunity in infected patients may provide novel information regarding the pathogenesis and prognosis of this infection. We used an ELISPOT assay to analyze a cross-section of HCV-infected humans. HCV-infected patients without cirrhosis, those with cirrhosis, and controls with other liver diseases were tested for recall responses to HCV Core and NS3 proteins. Peripheral blood lymphocytes (PBLs) from HCV-infected patients without cirrhosis responded to NS3 and Core proteins, producing predominantly IFN-gamma, with little IL-4 or IL-5, In contrast, PBLs from HCV-infected patients with cirrhosis responded to NS3, but not to the Core protein, suggesting a selectively altered immune state during cirrhosis. Our data provide support for the notion that HCV-specific IFN-gamma -producing immunity is important in the pathogenesis of progressing HCV-related disease. (C) 2001 Academic Press.
引用
收藏
页码:232 / 240
页数:9
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