Why do cytotoxic T lymphocytes fail to eliminate hepatitis C virus? Lessons from studies using major histocompatibility complex class I peptide tetramers

Author:

Lechner Franziska1,Sullivan John2,Spiegel Hans3,Nixon Douglas F.3,Ferrari Belinda2,Davis Andrew2,Borkowsky Bill4,Pollack Henry4,Barnes Ellie15,Dusheiko Geoff5,Klenerman Paul1

Affiliation:

1. Nuffield Department of Medicine, John Radcliffe Hospital, Oxford OX3 9DU, UK

2. Australian Red Cross Blood Service, 153 Clarence Street, Sydney 2000, Australia

3. Aaron Diamond AIDS Research Centre, Rockerfeller University, 455 First Avenue, NewYork, NY 10016, USA

4. Division of Paediatric Infectious Diseases, New Y ork University School of Medicine, 550 First Avenue, New Y ork, NY 10016, USA

5. Department of Medicine, Royal Free Hospital Medical School, Pond Street, London NW3 2Q J, UK

Abstract

Hepatitis C virus (HCV) infection is a major public health problem, affecting an estimated 3% of the world's population, and over 10% in some countries. Infection in most cases becomes persistent, and can lead to hepatic inflammation, fibrosis and liver failure. The T lymphocyte reponse, in particular that mediated by cytotoxic T lymphocytes (CTLs), is likely to be involved in determining the outcome of infection, although its overall role is not clear. The use of major histocompatibility complex (MHC) class I peptide tetrameric complexes (tetramers) to study antiviral CTL responses has revolutionized our approach to the study of human infection. We have used a panel of MHC class I tetramers to analyse immune responses in HCV–infected individuals at various stages of disease. We find that the CTL response against HCV is vigorous in its early phases but dwindles over time both in terms of lymphocyte number and function. A number of potential explanations for this ‘CTL failure’ are discussed.

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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