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
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.
引用
收藏
页码:563 / 572
页数:10
相关论文
共 37 条
[1]   HIV escape: there and back again [J].
Altman, JD ;
Feinberg, MB .
NATURE MEDICINE, 2004, 10 (03) :229-230
[2]   Adaptive immune responses in acute and chronic hepatitis C virus infection [J].
Bowen, DG ;
Walker, CM .
NATURE, 2005, 436 (7053) :946-952
[3]   Mutational escape from CD8+ T cell immunity:: HCV evolution, from chimpanzees to man [J].
Bowen, DG ;
Walker, CM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (11) :1709-1714
[4]   Immunological significance of cytotoxic T lymphocyte epitope variants in patients chronically infected by the hepatitis C virus [J].
Chang, KM ;
Rehermann, B ;
McHutchison, JG ;
Pasquinelli, C ;
Southwood, S ;
Sette, A ;
Chisari, FV .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (09) :2376-2385
[5]   Analysis of a successful immune response against hepatitis C virus [J].
Cooper, S ;
Erickson, AL ;
Adams, EJ ;
Kansopon, J ;
Weiner, AJ ;
Chien, DY ;
Houghton, M ;
Parham, P ;
Walker, CM .
IMMUNITY, 1999, 10 (04) :439-449
[6]   Cellular immune selection with hepatitis C virus persistence in humans [J].
Cox, AL ;
Mosbruger, T ;
Mao, Q ;
Liu, Z ;
Wang, XH ;
Yang, HC ;
Sidney, J ;
Sette, A ;
Pardoll, D ;
Thomas, DL ;
Ray, SC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (11) :1741-1752
[7]   Comprehensive analyses of CD8+T cell responses during longitudinal study of acute human hepatitis C [J].
Cox, AL ;
Mosbruger, T ;
Lauer, GM ;
Pardoll, D ;
Thomas, DL ;
Ray, SC .
HEPATOLOGY, 2005, 42 (01) :104-112
[8]   HLA-B27: portraying immunodominant viral epitopes [J].
de Castro, JAL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (02) :336-340
[9]   The outcome of hepatitis C virus infection is predicted by escape mutations in epitopes targeted by cytotoxic T lymphocytes [J].
Erickson, AL ;
Kimura, Y ;
Igarashi, S ;
Eichelberger, J ;
Houghton, M ;
Sidney, J ;
McKinney, D ;
Sette, A ;
Hughes, AL ;
Walker, CM .
IMMUNITY, 2001, 15 (06) :883-895
[10]   Late escape from an immunodominant cytotoxic T-lymphocyte response associated with progression to AIDS [J].
Goulder, PJR ;
Phillips, RE ;
Colbert, RA ;
McAdam, S ;
Ogg, G ;
Nowak, MA ;
Giangrande, P ;
Luzzi, G ;
Morgan, B ;
Edwards, A ;
McMichael, AJ ;
RowlandJones, S .
NATURE MEDICINE, 1997, 3 (02) :212-217