Our aim is to improve the health of people around the world through discovery of the basic mechanisms of disease and by finding and testing solutions to optimise health outcomes.

People in lower income countries suffer a high burden of health conditions, including diarrhoea, pneumonia, parasitic infections, anaemia, poor maternal child health, poor growth (stunting), and sub-optimal neurodevelopment.

Our research involves developing new cost-effective tools, treatments, diagnostics and health policies for the most challenging health problems facing people in low- and middle-income countries and to test solutions to these problems to help people in communities that need them most.

Some of our main disease priorities include:

• malaria
• tuberculosis
• HIV
• COVID-19
• maternal and child health
• anaemia
• parasites
• diarrhoea
• cancers

Our researchers working in global health span the spectrum of science, from advanced cutting-edge microbiological techniques through to large field randomised controlled trials.

We are conducting research that spans from molecular biology, immune response and systems biology to biomarker development, drug discovery and development to field studies, and from epidemiology, clinical trials to implementation science.

Our expertise includes diagnostic test development, clinical and epidemiological studies including large randomised controlled field trials and cohort studies, as well as policy development with organisations such as the World Health Organization (WHO).

We work across a broad range of countries including Brazil, Ecuador, South Africa, Malawi, Ethiopia, India, Pakistan, Bangladesh, Cambodia, Indonesia, Malaysia, Thailand, Philippines, Papua New Guinea, Solomon Islands and remote parts of Australia.

Our work is made possible thanks to the strong partnerships and collaborations we have with our colleagues in these countries. We also work with our local partners to provide training and build local capacity to meet research challenges.

We contribute to WHO policies by providing evidence and expert contributions to guideline processes, helping to set standards for health practices across the world.

For example, we have been designated the WHO Collaborating Centre for Anaemia Detection and Control and lead research and policy programs to reduce the prevalence of anaemia in low- and middle-income countries.

Epigenetics explains how cells are able to use different parts of their DNA at different times. Epigenetic modifications made to our DNA underpin many important processes in our bodies, and can be corrupted in disease.

Our epigenetics researchers aim to unravel how epigenetic changes influence healthy and diseased cells, with a goal of better treatments for diseases.

Our research in the field of epigenetics aims to:

• Discover new proteins that either package or epigenetically modify our DNA.
• Reveal how epigenetic changes control the development and function of different cell types in health and disease.
• Develop new strategies that treat disease by altering the epigenetic control of genes.

Epigenetics examines how our body manages to create all of our different cell types – such as white blood cells, muscle cells and skin cells – from the same genetic code. It studies how chemical changes, called ‘epigenetic modifications’ switch genes on or off.

Our genome, made of DNA, contains the instructions for how our cells behave. Different cells in our body function in distinct ways because of variations in the proteins made by each cell. The proteins are produced under instruction from genes. Switching different genes on or off affects which particular proteins are produced. For example, red blood cells produce haemoglobin to transport oxygen, whereas skin cells make elastin to keep our skin elastic.

DNA consists of four ‘letters’ called bases. It is the sequence of bases that makes the instructions within genes. Changes in the order of the bases changes the proteins that are produced.

Epigenetic modifications are chemical changes to DNA and to certain proteins, called histones, that DNA wraps around. The DNA and histones together are called ‘chromatin’.

Chemical changes influence whether the chromatin is:

• ‘Open’ or packed loosely, allowing genes to be active, or
• ‘Closed’ or packed tightly, inactivating the genes.

Epigenetic modifications are reversible: a cell can switch off a gene at one point in time, and switch it back on later. The trigger to open or close a particular section of DNA can be:

• An external signal received by the cell, such as a hormone binding to a receptor, or a change in a nutrient.
• An internal change in the cell, such as the cell preparing to divide.

When a cell divides, the ‘parent’ cell’s epigenetic state can be maintained in the daughter cells. This means that a trigger at one point in time can influence how a cell behaves at a later time. It also means that when a certain type of cell divides it produces another cell of the same type. Thus, a liver cell divides into two liver cells, not into any other type of cell.

The environment can also influence epigenetic modifications. In particular, it appears that changes to a mother’s diet are experienced by the developing foetus, and can influence how epigenetic modifications are established during development in the womb. This can influence the disease sensitivities of the person into adulthood.