Teresa Lambe
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Professor Teresa Lambe
PhD, OBE, FMedSci
Calleva Head of Vaccine Immunology
Associate Head of Department (People & Culture)
Professor Teresa Lambe is the Calleva Head of Vaccine Immunology and a Professor of Vaccinology & Immunology and PSI Investigator at the University of Oxford. She is leading a research group which improves human health by controlling disease through vaccination – stopping epidemics before they become pandemics.
Prof Lambe is one of the Principal Investigators overseeing the Oxford/AstraZeneca vaccine programme; she co-designed the vaccine in January 2020, led the preclinical studies, and then oversaw the delivery of the immune results needed to support regulatory approval in late 2020. The vaccine has played a pivotal role in the fight against COVID-19 – estimated to have saved >6 million lives globally in 2021 alone. Prof. Lambe was appointed as an honorary OBE for her services to Sciences and Public Health in the 2021 Queen’s Birthday Honours and recieved the Presidential Distinguished Service Award for the Irish Abroad in 2022.
Prof Lambe’s group are particularly interested in delineating the protective immune response post infection and using these findings to rationally design vaccination strategies to prevent disease. The establishment of long-lived immunity, post vaccination, is also critically important in protecting against infectious disease and is a key focus of the research.
The Lambe group is currently developing and testing vaccines against a number of outbreak pathogens including Crimean-Congo haemorrhagic fever virus, Ebola virus, Marburg virus Disease and Coronaviruses. A number of these vaccines have progressed to clinical trial assessment, including a vaccine against Ebola virus diseases (ChAdOx1 biEBOV); in late 2022, this vaccine was one of three chosen by the WHO to be included in a ring vaccination protocol against the Sudan ebolavirus outbreak in Uganda. In 2023, the team's candidate vaccine against Marburg virus disease was selected by WHO for inclusion in trials to combat Marburg virus disease.
Recent publications
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Safety and immunogenicity of the ChAdOx1 nCoV-19 (AZD1222) vaccine in children aged 6-17 years: Final results of a phase 2, single-blind, randomised controlled trial (COV006).
Li G. et al, (2025), Vaccine, 62
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Heterologous COVID-19 vaccine schedule with protein-based prime (NVX-CoV2373) and mRNA boost (BNT162b2) induces strong humoral responses: results from COV-BOOST trial.
Janani L. et al, (2025), J Infect
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Immunogenicity and Safety of ChAdOx1 nCoV-19 (AZD1222) as a Homologous Fourth-Dose Booster: A Substudy of the Phase 3 COV003 Trial in Brazil
Costa Clemens SA. et al, (2025), Mayo Clinic Proceedings Innovations Quality and Outcomes, 9
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Nipah virus vaccines evaluated in pigs as a 'One Health' approach to protect public health.
McLean RK. et al, (2025), NPJ Vaccines, 10
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Age differences in immunity to human seasonal coronaviruses and the immunogenicity of ChAdOx1 nCoV-19 (AZD1222).
Belij-Rammerstorfer S. et al, (2025), EBioMedicine, 118
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Complement-mediated enhancement of SARS-CoV-2 antibody neutralisation potency in vaccinated individuals.
Mellors J. et al, (2025), Nat Commun, 16
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Safety and immunogenicity of a bivalent Ebola virus and Sudan virus ChAdOx1 vectored vaccine in adults in the UK: an open-label, non-randomised, first-in-human, phase 1 clinical trial.
Jenkin D. et al, (2025), Lancet Microbe
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Safety and humoral immunogenicity of the ChAdOx1 nCoV-19 vaccine administered as a fourth dose booster following two doses of ChAdOx1 nCoV-19 and a third dose of BNT162b2 (COV009): A prospective cohort study.
Feng S. et al, (2025), J Infect, 90
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Translational science at the undergraduate level: awakening talents to overcome the valley of death - case report.
Ferreira RS. et al, (2025), J Venom Anim Toxins Incl Trop Dis, 31
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Predictors of severity of SARS-CoV-2 infections in Brazil: Post hoc analyses of a randomised controlled trial.
Conlin K. et al, (2024), Vaccine, 45