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Dominant influence of an HLA-B27 restricted CD8+ T cell response in mediating HCV clearance and evolution
被引:168
作者:
Neumann-Haefelin, C
McKiernan, S
Ward, S
Viazov, S
Spangenberg, HC
Killinger, T
Baumert, TF
Nazarova, N
Sheridan, I
Pybus, O
von Weizsäcker, F
Roggendorf, M
Kelleher, D
Klenerman, P
Blum, HE
Thimme, R
机构:
[1] Univ Freiburg, Dept Med 2, Freiburg, Germany
[2] St James Hosp, Dublin 8, Ireland
[3] Nuffield Dept Clin Med, Oxford, England
[4] Univ Essen Gesamthsch, Dept Virol, Essen, Germany
来源:
基金:
英国惠康基金;
关键词:
D O I:
10.1002/hep.21049
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Virus-specific CD8+ T cell responses play an important role in the natural course of infection; however, the impact of certain CD8+ T cell responses in determining clinical outcome has not been fully defined. A well-defined cohort of women inoculated with HCV from a single source showed that HLA-B27 has a strong association with spontaneous clearance. The immunological basis for this association is unknown. However, the finding is especially significant because HLA-B27 has also been shown to have a protective role in HIV infection. We report the identification of an HLA-B27 restricted hepatitis C virus (HCV)-specific CD8+ T cell epitope that is recognized in the majority of recovered HLA-B27 positive women. In chronically HCV-infected individuals, analysis of the corresponding viral sequence showed a strong association between sequence variations within this epitope and expression of HLA-B27, indicating allele-specific selection pressure at the population level. Functional analysis in 3 chronically HCV-infected patients showed that the emerging variant viral epitopes represent escape mutations. In conclusion, our results suggest a dominant role of HLA-B27 in mediating spontaneous viral clearance as well as viral evolution in HCV infection and mechanistically link both associations to a dominant novel CD8+ T cell epitope. These results support the central role of virus-specific CD8+ T cells and the genetically determined restriction of the virus-specific T cell repertoire in HCV infection.
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页码:563 / 572
页数:10
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