Dynamics of hypervariable region 1 variation in hepatitis C virus infection and correlation with clinical and virological features of liver disease

被引:49
作者
Brambilla, S
Bellati, G
Asti, M
Lisa, A
Candusso, ME
D'Amico, M
Grassi, G
Giacca, M
Franchini, A
Bruno, S
Ideo, G
Mondelli, MU
Silini, EM
机构
[1] Univ Pavia, Ist Anat Patol, Dept Pathol, I-27100 Pavia, Italy
[2] IRCCS, Policlin San Matteo, I-27100 Pavia, Italy
[3] Osped Niguarda Ca Granda, Hepatol Unit Crespi, Milan, Italy
[4] CNR, Ist Genet Biochim & Evoluzionist, Populat Genet Lab, I-27100 Pavia, Italy
[5] UN, Int Ctr Genet Engn & Biotechnol, Trieste, Italy
[6] Osped San Paolo, Dept Internal Med, Milan, Italy
[7] Univ Pavia, Dept Infect Dis, I-27100 Pavia, Italy
关键词
D O I
10.1002/hep.510270629
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatitis C virus (HCV) infection is a dynamic process during which molecular variants are continously selected as the result of virus adaptation to the host. Understanding the nature of HCV genetic variation is central to current theories of pathogenesis and immune response. We prospectively studied hypervariable region 1 (HVR1) variation in the E2 gene of 36 hepatitis C patients, including 10 asymptomatic carriers, fol lowed up for 1 to 2 years. Sequence changes in single and consecutive serum samples were assessed and correlated with clinical and virological parameters of liver disease. A region of the El gene was sequenced for comparison in 3 subjects, HVR1 heterogeneity at single time points widely varied in individual patients, did not increase cumulatively over the follow-up period, and did not correlate with HVR1 evolutionary rates, Conversely, the process of HVR1 sequence diversification, although differed considerably among patients, was stable over time and directly correlated with infections by HCV type 2, lower alanine aminotransferase (ALT) levels, and absence of cirrhosis, HCV carriers showed the highest HVR1 variation rates. Our findings indicate that HVR1 variation has an adaptive significance and is associated with favorable features of liver disease and suggest that prospective, rather than static, observations are required to model the process of HCV variation.
引用
收藏
页码:1678 / 1686
页数:9
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