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Informing the development of the next-generation malaria vaccines by:

  • identifying and characterising key functional mechanisms of antibodies that mediate protection,
  • defining the key cellular mechanisms that promote the generation of functional antibodies, and
  • quantifying the impact of host age and prior malaria exposure on antibody development.

Dr Michelle Boyle completed her PhD in 2012 at the Burnet Institute and Melbourne University with a focus on developing methods to study Plasmodium falciparum malaria invasion of red blood cells and progressing towards vaccine and drug development.

Following her PhD, Michelle was awarded an NHMRC Early Career (CJ Martin) Fellowship and completed a two-year post-doctoral position at the University of California, San Francisco. Her work identified a number of age and malaria exposure-dependent changes to T cells that contribute to naturally acquired immunity and she received the Australian National Association of Research Fellows Postdoctoral Investigator Award in 2015.

Dr Boyle is currently working on collaborative projects between the Menzies School of Health Research in Darwin, where she is an Honorary Fellow, and the Burnet Institute to identify mechanisms contributing to the acquisition of immunity against multiple malaria species in the South East Asia region.

She is also establishing her lab at the QIMR Berghofer Medical Research Institute in Queensland, where she will commence as an EMBL Australia Group Leader in early 2019.

Authors
Title
Published In

Boyle MJ et al. (2017)

Opposing roles for TNF and IL10 production by CD4 T cells in children in an area of high malaria transmission. 

Frontiers in Immunology, 8, 1329.

Boyle MJ et al. (2010)

Isolation of viable Plasmodium falciparum merozoites to define erythrocyte invasion events and advance vaccine and drug development.

Proc Natl Acad Sci USA, 107 (32), 14378-14383.

Boyle MJ et al. (2015)

Human antibodies fix complement to inhibit Plasmodium falciparum invasion of erythrocytes and are associated with protection against clinical malaria. 

Immunity, 42 (3) 580.

Boyle MJ et al. (2015)

Decline of FoxP3+ Regulatory CD4 T cells in peripheral blood of children heavily exposed to malaria.

Plos Pathog. 11, (7).