Hepatitis C Virus (HCV) Sequence Variation Induces an HCV-Specific T-Cell Phenotype Analogous to Spontaneous Resolution

Author:

Kasprowicz Victoria1,Kang Yu-Hoi2,Lucas Michaela2,Schulze zur Wiesch Julian3,Kuntzen Thomas1,Fleming Vicki2,Nolan Brian E.3,Longworth Steven3,Berical Andrew1,Bengsch Bertram4,Thimme Robert4,Lewis-Ximenez Lia5,Allen Todd M.1,Kim Arthur Y.1,Klenerman Paul2,Lauer Georg M.3

Affiliation:

1. Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts

2. Nuffield Department of Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, United Kingdom

3. Gastrointestinal Unit, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts

4. Medizinische Klinik, Universitaet Freiburg, Freiburg, Germany

5. Departmento de Virologia, Instituto Oswaldo Cruz/Fiocruz, Rio de Janeiro, RJ, Brazil

Abstract

ABSTRACT Hepatitis C virus (HCV)-specific CD8 + T cells in persistent HCV infection are low in frequency and paradoxically show a phenotype associated with controlled infections, expressing the memory marker CD127. We addressed to what extent this phenotype is dependent on the presence of cognate antigen. We analyzed virus-specific responses in acute and chronic HCV infections and sequenced autologous virus. We show that CD127 expression is associated with decreased antigenic stimulation after either viral clearance or viral variation. Our data indicate that most CD8 T-cell responses in chronic HCV infection do not target the circulating virus and that the appearance of HCV-specific CD127 + T cells is driven by viral variation.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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