Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

BACKGROUND:Induction of functional helper CD4+ T cells is the hallmark of a protective immune response against HCV, associated with spontaneous viral clearance. Heterologous prime/boost viral vectored vaccination has demonstrated induction of broad and polyfunctional HCV specific CD8+ T-cells in healthy volunteers, however much less is known about CD4+ T-cell subsets following vaccination. METHODS:We analysed HCV specific CD4+ T-cell populations using MHC Class II tetramers in volunteers undergoing HCV vaccination with novel recombinant HCV adenoviral/MVA viral vectors. Peptide-specific T cell responses were tracked over time and functional (proliferation and cytokine secretion) and phenotypic (cell surface and intranuclear) markers were assessed using flow cytometry. These were compared to CD4+ responses in 10 HLA-matched individuals with HCV spontaneous resolution and 21 chronically infected patients treated with directly acting antiviral therapy (DAA). RESULTS:Vaccination induced tetramer positive CD4+ T cells that were highest 1-4 weeks after boosting (mean 0.06%). Similar frequencies were obtained for those tracked following spontaneous resolution of disease (mean 0.04%). In addition, the cell surface phenotype (CD28, CD127) memory subset markers and intranuclear transcription factors, as well as functional capacity of peptide specific CD4+ T cell responses characterized after vaccination are comparable to those following spontaneous viral resolution. In contrast, helper responses in chronic infection were infrequently detected and poorly functional, and did not consistently recover following HCV cure. CONCLUSIONS:Helper CD4+ T-cell phenotype and function following HCV viral vectored vaccination resembles "protective memory" that is seen following spontaneous clearance of HCV. DAA cure does not promote resurrection of exhausted CD4+ T cell memory in chronic infection.

Original publication

DOI

10.1002/hep.31160

Type

Journal article

Journal

Hepatology (Baltimore, Md.)

Publication Date

03/02/2020

Addresses

University of Oxford, Peter Medawar Building for Pathogen Research, Oxford, United Kingdom.