Spatiotemporal Differences in Presentation of CD8 T Cell Epitopes during Hepatitis B Virus Infection

Author:

Khakpoor Atefeh1,Ni Yi23,Chen Antony4,Ho Zi Zong5,Oei Vincent1,Yang Ninghan6,Giri Reshmi1,Chow Jia Xin1,Tan Anthony T.1,Kennedy Patrick T.7,Maini Mala8,Urban Stephan23,Bertoletti Antonio16

Affiliation:

1. Emerging Infectious Diseases Program, Duke-NUS Medical School, Singapore, Republic of Singapore

2. Department of Infectious Diseases, Molecular Virology, University Hospital Heidelberg, Heidelberg, Baden-Württemberg, Germany

3. German Center for Infection Research, Heidelberg, Germany

4. Infectious Disease and Vaccines, Janssen Pharmaceuticals, Beerse, Belgium

5. Lion TCR Private Limited, Singapore, Republic of Singapore

6. Singapore Immunology Network, A*STAR, Singapore, Republic of Singapore

7. Hepatology, Centre for Immunobiology, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom

8. Division of Infection and Immunity, University College London, London, United Kingdom

Abstract

The inability of patients with chronic HBV infection to clear HBV is associated with defective HBV-specific CD8 + T cells. Hence, the majority of immunotherapy developments focus on HBV-specific T cell function restoration. However, knowledge of whether distinct HBV-specific T cells can equally target all the HBV-infected hepatocytes of a chronically infected liver is lacking. In this work, analysis of CHB patient liver parenchyma and in vitro HBV infection models shows a nonuniform distribution of HBV CD8 + T cell epitopes that is influenced by the presence of IFN-γ and availability of newly translated viral antigens. These results suggest that CD8 + T cells recognizing different HBV epitopes can be necessary for efficient immune therapeutic control of chronic HBV infection.

Funder

MOH | National Medical Research Council

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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