Our work strives to understand malaria infection and vaccination.
Our group aims to understand the key cellular mechanisms that lead to protective immunity in response to malaria infection and vaccination and to discover why these cells are less responsive in children and in those with prior malaria infection.
Long term, our research aims to develop novel therapeutics that can boost protective immunity during malaria infection or vaccination.
We're using germinal centre organoid models to investigate human immune development to malaria parasites and malaria vaccines.
Understanding immune development in this unique clinical trial will help us develop approaches to boost protective immunity to malaria, leading to novel therapeutics.
Understanding immune development to the COVID-19 virus (SARS-CoV-2) in areas of high malaria transmission will inform future COVID-19 control strategies and underlying immune development.
EBioMedicine
Reena Mukhiya, Jessica R. Loughland, Jo-Anne Chan, James G. Beeson, Michelle J. Boyle
Nature reviews. Immunology
Michelle J. Boyle
Nature Communications
Julianne Hamelink
Nature Communications
Jo-Anne Chan
EBioMedicine
Jo-Anne Chan, Bruce D. Wines, P. Mark Hogarth, James G. Beeson, Michelle J. Boyle
Cell Reports Medicine
Nicholas Dooley, Jo-Anne Chan, Bruce D. Wines, P. Mark Hogarth, James G. Beeson, Michelle J. Boyle, Jo-Anne Chan, Bruce D. Wines, P. Mark Hogarth, James G. Beeson
Science Advances
A M Hilton, Michelle J. Boyle, Jo-Anne Chan, Linda Reiling, Gaoqian Feng, Liriye Kurtovic, Christine Langer, Damien R. Drew, Freya J. I. Fowkes, James G. Beeson
JCI Insight
James G. Beeson, Michelle J. Boyle
The Journal of Infectious Diseases
Danny W. Wilson, Freya J. I. Fowkes, James G. Beeson, Michelle J. Boyle
Antimicrobial Agents and Chemotherapy
Michelle J. Boyle, Benjamin K. Dickerman, James G. Beeson
Frontiers in Immunology
Michelle J. Boyle
The Journal of Infectious Diseases
Michelle J. Boyle
PLoS Pathogens
Michelle J. Boyle
Immunity
Linda Reiling, Michelle J. Boyle, Gaoqian Feng, Christine Langer, Yang Cheng, Janine Stubbs, James G. Beeson, Janine Stubbs, Michelle J. Boyle, Linda Reiling
Infection and Immunity
Michelle J. Boyle, Christine Langer, Jo-Anne Chan, James G. Beeson
Research Square (Research Square)
Michelle J. Boyle, James G. Beeson
Blood
Paul R. Gilson
Michelle Boyle, David Wilson, James Beeson
6th edition, 2013, EVIMalaR Glasgow, UK, edited by Moll K, Kaneko A, Scherf A, Wahlgren M.
Michelle Boyle, David Wilson, James Beeson
6th edition, 2013, EVIMalaR Glasgow, UK, edited by Moll K, Kaneko A, Scherf A, Wahlgren M
This SOP describes processing blood samples from donors to isolate plasma, peripheral blood mononuclear cells (PBMCs), and fixed whole blood for storage. Blood samples can be from volunteer donors or buffy coat blood samples from Australian Red Cross Life Blood donors.
Boylelab SOP RA Blood Sample Processing 0 BThis SOP provides a guide for stimulating PBMC/Spleen/Tonsil cells and measuring activation-induced markers (AIMs) to determine antigen-specific response. PBMC/Spleen/Tonsil samples are stimulated with Plasmodium-parasitised red blood cells (pRBCs) to investigate malaria-specific cellular response.
Boylelab SOP AIM [PDF 315.4 kB]This SOP describes the process of the continuous in vitro culturing of Plasmodium falciparum erythrocytic stages in human red blood cells (RBCs).
Boylelab SOP Plasmodium Culture [PDF 325.8 kB]This SOP describes the process of stimulating human whole blood ex vivo, or cryopreserved PMBC, spleen, and/or tonsil cells.
Boylelab SOP PMA Stimulation [PDF 467.7 kB]This SOP provides guide for ex vivo fluorescent cell staining of cryopreserved human PBMC/Spleen/Tonsil cells. The cell staining involves staining process for cell surface and intracellular markers labelled with fluorochrome-conjugated antibodies. Cell markers can be used to identify cell subsets based on lineage, differentiation state, and function.
Boylelab SOP RA Ex Vivo Cell Staining [PDF 137.3 kB]Cryopreserved PBMC/Spleen/Tonsils cells are sensitive to the thawing processes. To ensure optimal cell recovery and viability, thaw protocols are optimised.
Boylelab SOP RA PBMC Thaw [PDF 131.0 kB]This SOP provides a guide for the generation of in vitro organoids using human tonsil/spleen cell suspensions. Here, tonsils or spleen organoids will be used as in vitro functional systems that mimic key features of the germinal centres in vivo.
Boylelab SOP Tonsil Organoids [PDF 184.4 kB]This SOP describes the process of isolating cells from tonsils, followed by storage in liquid nitrogen.
Boylelab SOP Tonsils Processing [PDF 144.3 kB]