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Intrahepatic CD8 + T‐cell failure during chronic hepatitis C virus infection
Author(s) -
Spangenberg Hans Christian,
Viazov Sergei,
Kersting Nadine,
NeumannHaefelin Christoph,
McKinney Denise,
Roggendorf Michael,
von Weizsäcker Fritz,
Blum Hubert E.,
Thimme Robert
Publication year - 2005
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.20856
Subject(s) - hepatitis c virus , cd8 , epitope , cytotoxic t cell , immunology , virus , t cell , virology , biology , hepatology , medicine , immune system , antibody , in vitro , biochemistry
The precise mechanisms responsible for the failure of intrahepatic hepatitis C virus (HCV)‐specific CD8 + T cells to control the virus during persistent infection have not been fully defined. We therefore studied the CD8 + T‐cell response in 27 HLA‐A2–positive patients using four previously well‐defined HLA‐A2–restricted HCV epitopes. The corresponding HCV sequences were determined in several patients and compared with the intrahepatic HCV‐specific CD8 + T‐cell response. The results of the study indicate: (1) intrahepatic HCV‐specific CD8 + T cells are present in the majority of patients with chronic HCV infection and overlap significantly with the response present in the peripheral blood. (2) A large fraction of intrahepatic HCV‐specific CD8 + T cells are impaired in their ability to secrete interferon γ (IFN‐γ). This dysfunction is specific for HCV‐specific CD8 + T cells, since intrahepatic Flu‐specific CD8 + T cells readily secrete this cytokine. (3) T‐cell selection of epitope variants may have occurred in some patients. However, it is not an inevitable consequence of a functional virus‐specific CD8 + T‐cell response, since several patients with IFN‐γ–producing CD8 + T‐cell responses harbored HCV sequences identical or cross‐reactive with the prototype sequence. (4) The failure of intrahepatic virus–specific CD8 + T cells to sufficiently control the virus occurs despite the presence of virus‐specific CD4 + T cells at the site of disease. In conclusion , different mechanisms contribute to the failure of intrahepatic CD8 + T cells to eliminate HCV infection, despite their persistence and accumulation in the liver. (H EPATOLOGY 2005;42:828–837.)

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