Heterologous T cell immunity in severe hepatitis C virus infection

被引:108
|
作者
Urbani, S
Amadei, B
Fisicaro, P
Pilli, M
Missale, G
Bertoletti, A
Ferrari, C [1 ]
机构
[1] Azienda Osped Univ Parma, Dept Infect Dis & Hepatol, Lab Viral Immunopathol, I-43100 Parma, Italy
[2] UCL, Inst Hepatol, London WC1E 6HX, England
[3] Ist Nazl Malattie Infett Lazzaro Spallanzani, I-00149 Rome, Italy
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 2005年 / 201卷 / 05期
关键词
D O I
10.1084/jem.20041058
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hepatitis C virus (HCV) can cause liver disease of variable severity. Expansion of preexisting memory CD8 T cells by cross-reactivity with a new heterologous virus infection has been shown in mice to shape the repertoire of the primary response and to influence virus-related immunopathology (Selin, L.K. 2004. Immunity. 20:5-16). To determine whether this mechanism can influence the course of HCV infection, we analyzed the features of the HCV-specific CD8 T cell response in eight patients with acute HCV infection, two of whom had a particularly severe illness. Patients with severe hepatitis, but not those with mild disease, showed an extremely vigorous CD8 T cell response narrowly focused on a single epitope (NS3 1073-1081), which cross-reacted with an influenza neuraminidase sequence. Our results suggest that CD8 T cell cross-reactivity influences the severity of the HCV-associated liver pathology and depicts a model of disease induction that may apply to different viral infections.
引用
收藏
页码:675 / 680
页数:6
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