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
Heterologous mucosal vaccine boosting enhances mucosal and systemic immunity by distinct mechanisms.
Journal article
Bissett C. et al, (2026), The Journal of experimental medicine, 223
Time to tackle vaccine-HLA associations with artificial intelligence.
Journal article
Mentzer AJ. et al, (2026), The Lancet. Infectious diseases, 26
Reactogenicity and immunogenicity following heterologous and homologous third dose COVID-19 vaccination in UK adolescents (Com-COV3): A randomised controlled non-inferiority trial.
Journal article
Kelly E. et al, (2026), The Journal of infection, 92
Early lymph node T follicular helper cell signalling hub drives influenza vaccine response in an ancestrally diverse cohort
Journal article
Siu JHY. et al, (2025), eBioMedicine, 122, 106036 - 106036
Drivers of Crimean-Congo Hemorrhagic Fever in Natural Host and Effects of Control Measures, Bulgaria.
Journal article
Limon G. et al, (2025), Emerging infectious diseases, 31, 1738 - 1746
Heterologous COVID-19 vaccine schedule with protein-based prime (NVX-CoV2373) and mRNA boost (BNT162b2) induces strong humoral responses: Results from COV-BOOST trial.
Journal article
Janani L. et al, (2025), The Journal of infection, 91
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
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
Immunogenicity and Safety of ChAdOx1 nCoV-19 (AZD1222) as a Homologous Fourth-Dose Booster: A Substudy of the Phase 3 COV003 Trial in Brazil
Journal article
Costa Clemens SA. et al, (2025), Mayo Clinic Proceedings: Innovations, Quality & Outcomes, 9, 100642 - 100642
ge differences in immunity to human seasonal coronaviruses and the immunogenicity of ChAdOx1 nCoV-19 (AZD1222)
Journal article
Belij-Rammerstorfer S. et al, (2025), eBioMedicine, 118, 105847 - 105847