Vigorous peripheral blood cytotoxic T cell response during the acute phase of hepatitis C virus infection

被引:70
作者
Cucchiarini, M [1 ]
Kammer, AR
Grabscheid, B
Diepolder, HM
Gerlach, TJ
Grüner, N
Santantonio, T
Reichen, J
Pape, GR
Cerny, A
机构
[1] Univ Hosp Bern, Inselspital, Dept Clin Res, CH-3010 Bern, Switzerland
[2] Univ Hosp Bern, Inselspital, Inst Clin Pharmacol, CH-3010 Bern, Switzerland
[3] Univ Munich, Inst Immunol, D-8000 Munich, Germany
[4] Univ Bari, Sch Med, Clin Infect Dis, Bari, Italy
关键词
HCV; acute disease; CD8-positive lymphocytes; epitopes; T-lymphocyte; MHC class I;
D O I
10.1006/cimm.2000.1683
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
After infection by hepatitis C virus (HCV), a minority of patients develop acute symptomatic disease and some of them are able to clear the virus. In this study, we analyzed peripheral blood mononuclear cells from nine patients with acute symptomatic disease with respect to their cytotoxic T lymphocyte (CTL) response using a panel of HCV-derived peptides in a semiquantitative secondary in vibro culture system. We could detect early CTL responses in 67% of these patients. The CTL responses were directed against multiple viral epitopes, in particular within the structural (core 2-9, core 35-44, core 131-140, and core 178-187) and nonstructural regions of the virus (NS3 1073-1081, NS3 1406-1415, NS4 1807-1816, NS5 2252-2260, and NS5B 2794-2802). We compared the CTL responses displayed by recently and chronically infected HLA-A2-positive patients. Virus-specific CTLs were detectable in chronic carriers but the percentage of positive peptide-specific CTL responses was significantly higher in recently infected patients (P = 0.002). Follow-up of recently infected patients during subsequent disease development showed a significant decrease in the values and proportions of positive peptide-specific CTL responses (P = 0.002 and 0.013, respectively). Patients with limited viral replication exhibited significantly more vigorous early responses (P = 0.024). These data suggest a protective role for the early antiviral CTL response in HCV infection. (C) 2000 Academic Press.
引用
收藏
页码:111 / 123
页数:13
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