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- A multi-pronged approach to targeting myeloproliferative neoplasms
- A new paradigm of machine learning-based structural variant detection
- A whole lot of junk or a treasure trove of discovery?
- Advanced imaging interrogation of pathogen induced NETosis
- Analysing the metabolic interactions in brain cancer
- Atopic dermatitis causes and treatments
- Boosting the efficacy of immunotherapy in lung cancer
- Building a cell history recorder using synthetic biology for longitudinal patient monitoring
- Characterisation of malaria parasite proteins exported into infected liver cells
- Deciphering the heterogeneity of the tissue microenvironment by multiplexed 3D imaging
- Defining the mechanisms of thymic involution and regeneration
- Delineating the molecular and cellular origins of liver cancer to identify therapeutic targets
- Developing computational methods for spatial transcriptomics data
- Developing drugs to block malaria transmission
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- Developing statistical frameworks for analysing next generation sequencing data
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- Discovering epigenetic silencing mechanisms in female stem cells
- Discovery and targeting of novel regulators of transcription
- Dissecting host cell invasion by the diarrhoeal pathogen Cryptosporidium
- Dissecting mechanisms of cytokine signalling
- Doublecortin-like kinases, drug targets in cancer and neurological disorders
- Epigenetic biomarkers of tuberculosis infection
- Epigenetics – genome wide multiplexed single-cell CUT&Tag assay development
- Exploiting cell death pathways in regulatory T cells for cancer immunotherapy
- Exploiting the cell death pathway to fight Schistosomiasis
- Finding treatments for chromatin disorders of intellectual disability
- Functional epigenomics in human B cells
- How do nutrition interventions and interruption of malaria infection influence development of immunity in sub-Saharan African children?
- Human lung protective immunity to tuberculosis
- Improving therapy in glioblastoma multiforme by activating complimentary programmed cell death pathways
- Innovating novel diagnostic tools for infectious disease control
- Integrative analysis of single cell RNAseq and ATAC-seq data
- Interaction with Toxoplasma parasites and the brain
- Interactions between tumour cells and their microenvironment in non-small cell lung cancer
- Investigation of a novel cell death protein
- Malaria: going bananas for sex
- Mapping spatial variation in gene and transcript expression across tissues
- Mechanisms of Wnt secretion and transport
- Multi-modal computational investigation of single-cell communication in metastatic cancer
- Nanoparticle delivery of antibody mRNA into cells to treat liver diseases
- Naturally acquired immune response to malaria parasites
- Organoid-based discovery of new drug combinations for bowel cancer
- Organoid-based precision medicine approaches for oral cancer
- Removal of tissue contaminations from RNA-seq data
- Reversing antimalarial resistance in human malaria parasites
- Role of glycosylation in malaria parasite infection of liver cells, red blood cells and mosquitoes
- Screening for novel genetic causes of primary immunodeficiency
- Single-cell ATAC CRISPR screening – Illuminate chromatin accessibility changes in genome wide CRISPR screens
- Spatial single-cell CRISPR screening – All in one screen: Where? Who? What?
- Statistical analysis of single-cell multi-omics data
- Structural and functional analysis of epigenetic multi-protein complexes in genome regulation
- Structural basing for Wnt acylation
- Structure, dynamics and impact of extra-chromosomal DNA in cancer
- Targeted deletion of disease-causing T cells
- Targeting cell death pathways in tissue Tregs to treat inflammatory diseases
- The cellular and molecular calculation of life and death in lymphocyte regulation
- The role of hypoxia in cell death and inflammation
- The role of ribosylation in co-ordinating cell death and inflammation
- Understanding Plasmodium falciparum invasion of red blood cells
- Understanding cellular-cross talk within a tumour microenvironment
- Understanding the genetics of neutrophil maturation
- Understanding the roles of E3 ubiquitin ligases in health and disease
- Unveiling the heterogeneity of small cell lung cancer
- Using combination immunotherapy to tackle heterogeneous brain tumours
- Using intravital microscopy for immunotherapy against brain tumours
- Using nanobodies to understand malaria invasion and transmission
- Using structural biology to understand programmed cell death
- Validation and application of serological markers of previous exposure to malaria
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Hepatitis B

One-third of the world’s population has been infected with the hepatitis B virus. Most people experience only a short, mild disease, but a lifelong ‘chronic’ infection occurs in some people.
Hepatitis B puts people at risk of liver disease and cancer. Our hepatitis B research focuses on understanding how chronic infections occur, and how they can be cured.
Our hepatitis B research
Our researchers are investigating why the immune system cannot eliminate chronic hepatitis B infections. This is leading to new strategies to cure hepatitis B by stimulating immune clearance of the virus.
What is hepatitis B?
Hepatitis B is a liver disease caused by infection with the hepatitis B virus. In the short term this causes liver inflammation, which can cause illness and is occasionally fatal.
In most people, this ‘acute’ infection can be controlled within several months. This means the virus is no longer reproducing within the liver, and the person is no longer infectious.
In some people, the hepatitis B virus continues to grow within their liver cells. This is called a chronic infection. It can cause cirrhosis, a scarring of the liver that impairs its function.
Both acute and chronic hepatitis B infections put people at risk of developing liver cancer. The presence of the viral genome within liver cells can increase the chances that the liver cells develop genetic changes, allowing cancer development.
People who are at greater risk of developing chronic hepatitis B after initial infection include:
One-third of the world’s population has been infected with hepatitis B virus. The virus is carried as a chronic infection by 250 million people, including more than 230,000 Australians. Chronic hepatitis B infection is more prevalent in Aboriginal and Torres Strait Islander Australians than the wider population.
More than 880,000 people die each year from the consequences of hepatitis B infection. The prevalence of hepatitis B virus globally contributes to liver cancer being one of the leading causes of cancer-related deaths. In Australia, the number of deaths from liver cancer is increasing faster than deaths from any other cancer.
How is hepatitis B spread?
Hepatitis B virus is spread between people through infected blood and bodily fluids, such as semen and saliva. When hepatitis B virus enters the body, it infects liver cells. Here the virus can replicate, and release new viruses into the blood stream.
How can hepatitis B be prevented?
There is a vaccine that can protect against hepatitis B virus infection. It triggers the production of antibodies to hepatitis B virus. This prevents newly acquired virus from surviving within the body.
In Australia, hepatitis vaccination is recommended for:
- Newborns.
- People working in close contact with other people, such as healthcare and childcare workers.
- People living with someone infected with hepatitis B
- People with weakened immune systems, such as people with HIV.
How is hepatitis B treated?
Unvaccinated people who may have been exposed to hepatitis B virus can be treated with antibodies to hepatitis B. These antibodies bind to hepatitis B virus in the body, preventing them from infecting cells. The antibodies are produced from the donated blood of people who have been vaccinated against hepatitis B.
Acute hepatitis B is usually a mild illness that does not require treatment.
People who have chronic hepatitis B infection can be treated with antiviral medications. These do not cure the disease. Instead they reduce the growth of the virus, and reduce liver damage. Our researchers aim to discover how the immune system can be triggered to cure chronic hepatitis B infection.
Serious liver damage caused by hepatitis B is sometimes treated by liver transplantation.
Researchers:
Super Content:
A newly discovered gene could hold the key to treating and potentially controlling HIV, hepatitis and tuberculosis.
Dr Greg Ebert has won the Bupa Health Foundation Emerging Health Researcher Award 2014
Sylvia and Charles Viertel Fellowship to support Professor Marc Pellegrini's research into HIV, tuberculosis and hepatitis B
Read our latest update on research using birinapant to treat hepatitis B