Welcome 2024 Lister Prize Fellows
17 June 2024 / Blog Lister Institute Fellows
17 June 2024 / Blog Lister Institute Fellows
Announcing the annual Lister Prize winners is one of the highlights of our calendar, and 2024 is no exception. This year we welcome six new Lister Fellows, each one an exceptional early-career researcher in biomedical science. Lister Prize recipients each receive a lump sum of £300,000 to spend on furthering their research, which can be flexibly spent on staffing, equipment and other research costs.
University of Cambridge
Alex’s group studies rotaviruses, which cause over 170,000 child deaths annually. These RNA viruses are unique due to their segmented genomes, comprising eleven distinct chromosomes. He aims to uncover how rotaviruses and similar viruses assemble their genomic segments. This involves characterising RNA structures and sequences in genome assembly and investigating the molecular mechanisms of the formation of viral replication factories, where the assembly takes place in cells. His research seeks to identify universal genome assembly mechanisms in segmented viruses, providing new avenues for the development of treatments and improved vaccines.
Learn more about Alex’s work: https://www.borodavkalab.org/
Follow Alex on Twitter/X @AlexBoRNA
University of Glasgow
Andrew is interested in tumour cell death and how it shapes the tumour microenvironment. While killing tumour cells is the objective of most cancer therapies, our bodies are designed to respond to cell death by triggering healing, which the tumour can hijack to fuel relapse.
Furthermore, a failure to clear cell death triggers chronic inflammation, which cancer thrives in. Andrew’s lab combines the unrivalled genetics of Drosophila with powerful live-cell imaging to study tumour cell death and its clearance in vivo.
Follow Andrew on Twitter/X @Davidsndeathlab
Dr Sarah Dimeloe
University of Birmingham
Sarah is an immunologist with a particular interest in understanding the metabolism of our immune cells. Metabolism describes how cells take up nutrients and break them down to provide energy and building blocks. This changes dramatically in immune cells when they become engaged in a protective immune response. Sarah aims to understand exactly how this happens, since it is frequently dysregulated in diseases associated with altered immune cell function, including autoimmunity and cancer.
Learn more about Sarah’s work: https://www.birmingham.ac.uk/staff/profiles/immunology-immunotherapy/dimeloe-sarah
Follow Sarah on Twitter/X @SarahDimeloeLab
University of Birmingham
Rebecca’s research focus is invasive fungal infections, which kill a large number of vulnerable people every year. She predominantly studies the yeast Cryptococcus neoformans, which is a common cause of brain infection in people with HIV/AIDS. Her work looks at how this fungus grows in the brain, such as how it gains nutrients and avoids detection by the immune system, whilst also examining the antifungal immune response to unpick the host-fungal interactions occurring in the brain during an infection.
Learn more about Rebecca’s work: https://www.birmingham.ac.uk/staff/profiles/immunology-immunotherapy/drummond-rebecca
Follow Rebecca on Twitter/X @theRAD_lab
University College London
Juvenile idiopathic arthritis (JIA) is the most common childhood disease of the joints, with a UK prevalence of 1 in 1000. For unknown reasons, some JIA patients develop uveitis, an inflammatory disorder of the eye, which can lead to life-long loss of sight. Lizzy’s group is investigating how different B cell populations contribute to joint, and now through the Lister Prize, eye damage in JIA. Understanding the contribution of B cells to uveitis pathology could lead to the development of novel B-cell targeted therapeutic strategies that prevent visual impairment in these children.
Learn more about Lizzy’s’s work: https://profiles.ucl.ac.uk/6466-lizzy-rosser
Follow Lizzy on Twitter/X @bcells_rosser
University of Oxford
Over 300 million people globally have a rare disease and 80% of rare diseases are thought to be genetic. Currently, disease-causing genetic mutations are only looked for in the 1.5% of our DNA that directly encodes proteins. But through this approach, we find the genetic cause of disease for less than half of all rare disease patients. Nicky’s team researches genetic variants outside of protein-coding regions of the DNA (in the other 98.5%) to find new diagnoses for patients and to understand more about gene regulation.
Learn more about Nicky’s’s work: www.rarediseasegenomics.org/
Follow Nicky on Twitter/X @nickywhiffin
Applications for the 2025 Prize will open on 8th July 24 and will remain open until 23rd September. We welcome applications from early-career biomedical researchers across the UK and the Republic of Ireland who feel that the funding would make a major difference to their work.
The Prize includes £300,000 (awarded as a lump sum grant) that must be spent within five years. It is completely flexible and can be used for any research costs and expenses, including the salaries of post-doctoral workers, technicians, or PhD students, but not the winner’s own salary.
Please keep an eye on the website and follow us on Twitter/X and LinkedIn for further announcements.