Ellie (Eleanor) Barnes
BSc. MBBS. PhD, FRCP. FMedSci.
Professor of Hepatology and Experimental Medicine
Tackling Cancer and Complex Pathogens Through Vaccine Innovation and Early Cancer Detection
The Barnes group is an established research group with a focus on vaccines for complex viral pathogens and cancer, applied immunology, and cancer detection. We seek to translate laboratory and clinical findings through to human experimental medicine studies.
We focus on the development, optimisation, and evaluation of novel vaccines, targeting some of the most challenging infectious diseases and cancers, using mRNA/LNPs and viral vectors. The development of vaccines against both cancer and complex pathogens face shared challenges including antigenic diversity, within-host variation, and immune evasion.
We have designed and developed vaccines for oncogenic Hepatitis B and C viruses, taking candidates from concept through to human trials, sometimes co-administered with check-point blockade in humans. We utilise immune responses during natural infection and or pre-cancer, to inform rational vaccine design. We are developing T cell–based pan-coronavirus vaccines and analyse responses to vaccines in patients with chronic diseases. We play a leading role in preventative cancer vaccine research at Oxford including the Oxford–GSK Immuno-Prevention Programme and the Lynch-Vax cancer vaccine program. The group integrates T cell and B cell immunology, mRNA and viral vector vaccine platforms, and advanced molecular and computational immunology to address the challenges in vaccine development.
Key questions of current focus within the group are: (i) Which antigens are most conserved and relevant across hosts? (ii) How do antigen expression and localisation influence immune recognition? (iii) Can we engineer vaccine constructs to overcome immune evasion? (iv) How does disease state affect immune recognition of vaccine antigens.
The lab uses state-of-the-art immunological and molecular techniques, including multi-parametric flow cytometry and ELISpot, Intracellular cytokine staining, scRNA-seq and transcriptomic analysis of antigen specific T cells, B cell isolation, BCR sequencing, and monoclonal antibody production, alongside vaccine design and generation and the assessment of antigen expression and immunogenicity in small animal models and humans.
With investigators at the Ludwig and the Cancer Centre, we take an inter-disciplinary approach to develop new technologies for liver cancer early detection, funded by CRUK. For this we use spatial proteomics and transcriptiomics alongside novel imaging and molecular technologies for cancer diagnosis and risk. In Autumn 2025 we are moving to the Centre for Immuno-Oncology in the NDMRB, Old Road Campus site.
Leadership roles include: member of Joint Committee for Vaccines and Immunisation (JCVI), co-lead Oxford NIHR BRC Life Saving vaccine theme, lead for the Oxford Liver Cancer Centre of Excellence (CELESTE), CI for the CRUK program in liver cancer (HCC) early detection (DeLIVER programme developing novel detection methodologies for the identification of HCC), co-director of the Oxford-GSK Go-Precise Alliance, lead for the NDM Career Development Fellowship scheme and NIHR Senior Investigator. Ellie continues to care for patients with advanced liver disease at OUH NHS Hospital Trust. She is accredited as a hospital consultant in hepatology and general medicine.
Recent publications
Risk Factors of Metabolic Dysfunction-associated Steatotic Liver Disease in a Cohort of Patients With Chronic Hepatitis B
Journal article
Kalafateli M. et al, (2026), Clinical Gastroenterology and Hepatology, 24, 701 - 712.e8
CE2 inhibition ELISA is an effective surrogate for SARS-CoV-2 live virus neutralisation
Journal article
Tipton T. et al, (2026), Vaccine, 72, 128123 - 128123
Response to Comments on ‘Hepatitis B Virus ( HBV ) Treatment Eligibility in the UK : Retrospective Longitudinal Cohort Data to Explore the Impact of Changes in Clinical Guidelines’
Journal article
Campbell C. et al, (2026), Journal of Viral Hepatitis, 33
ssociation between COVID-19 vaccine immunogenicity and protection against infection and severe disease in clinically vulnerable patient populations: a systematic review and meta-analysis of observational studies
Journal article
Danysz M. et al, (2026), Clinical Microbiology and Infection, 32, 41 - 55
Characterisation of People Living With Chronic Hepatitis B Virus Infection in England and Stratification by HBsAg Levels: A Cross‐Sectional Study
Journal article
Drysdale M. et al, (2025), Journal of Viral Hepatitis, 32
Dynamic impact of bivalent COVID-19 vaccine boosters on systemic and mucosal antibody and T cell immunity
Journal article
Kronsteiner B. et al, (2025), Scientific Reports, 15
The development of a pan-genotypic T cell vaccine against hepatitis C virus using heterologous prime-boost strategies
Journal article
Strain R. et al, (2025), Hepatology
HCV response-guided therapy: is shorter always better? – Authors' reply
Journal article
Cooke GS. et al, (2025), The Lancet, 406, 2540 - 2540
Hepatitis B Virus ( HBV ) Treatment Eligibility in the UK : Retrospective Longitudinal Cohort Data to Explore the Impact of Changes in Clinical Guidelines
Journal article
Campbell C. et al, (2025), Journal of Viral Hepatitis, 32
Genome-wide association and gene-virus interaction study of liver disease in hepatitis C virus-infected patients
Preprint
Quistrebert J. et al, (2025)
Interplay of host and viral genetic variations in modulating antibody responses to genotype 3a hepatitis C virus: Implications for vaccine design
Journal article
Wang Z. et al, (2025), Cell Reports, 44, 116418 - 116418
Evaluation of Hepatitis B core-related antigen (HBcrAg) as a biomarker in cohorts from the United Kingdom and South Africa
Journal article
Downs LO. et al, (2025), Journal of Infection, 91, 106601 - 106601
Dosing interval is a major factor determining the quality of T cells induced by SARS-CoV-2 mRNA and adenoviral vector vaccines
Journal article
Murray SM. et al, (2025), Science Immunology, 10
MAIT and other innate-like T cells integrate adaptive immune responses to modulate interval-dependent reactogenicity to mRNA vaccines
Journal article
Amini A. et al, (2025), Science Immunology, 10
Human tonsil organoids reveal innate pathways modulating humoral and cellular responses to ChAdOx1
Journal article
Pudjohartono MF. et al, (2025), PLOS Pathogens, 21, e1013432 - e1013432
Treatment options to support the elimination of hepatitis C: an open-label, factorial, randomised controlled non-inferiority trial
Journal article
Cooke GS. et al, (2025), The Lancet, 405, 1769 - 1780
Dynamic impact of bivalent COVID-19 vaccine boosters on systemic and mucosal immunity– an observational cohort study
Preprint
Dunachie S. et al, (2025)
Genetically distinct within-host subpopulations of hepatitis C virus persist after Direct-Acting Antiviral treatment failure
Journal article
Zhao L. et al, (2025), PLOS Pathogens, 21, e1012959 - e1012959
Complement-mediated enhancement of SARS-CoV-2 antibody neutralisation potency in vaccinated individuals
Journal article
Mellors J. et al, (2025), Nature Communications, 16
Whole genome sequencing of hepatitis B virus using tiled amplicon (HEPTILE) and probe based enrichment on Illumina and Nanopore platforms
Journal article
Lumley SF. et al, (2025), Scientific Reports, 15