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Field of Research : Gastroenterology and Hepatology
Research Topic : NK1.1+ T CELLS
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  • Funded Activity

    Appendicitis, Protection Again Colitis And The Role Of Colonic Regulatory T Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $67,381.00
    Summary
    The appendix has been regarded as a useless organ, however, there are evidence showing its removal reduces the risk of developing inflammatory bowel disease. We have shown that this may be due to altered intestinal immune regulation. The project plans to explore the mechanisms responsible for this altered immune regulation. With knowledge of specific elements of disease causation gained from these studies, more effective and targeted treatment options will become available.
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    Funded Activity

    When Prometheus Needs A Hand – How Human Amnion Epithelial Cells Resolve Fibrosis And Regenerate The Liver

    Funder
    National Health and Medical Research Council
    Funding Amount
    $530,653.00
    Summary
    Cirrhosis can progress to end stage disease for which transplantation provides the only hope for survival. Liver donors in Australia are scarce; the need for donor organs is increasing. Using stem cells to repair and regenerate damaged liver may provide an alternative to organ transplantation. We are studying placental stem cells that can decrease inflammation and increase progenitor cells to repair and regenerate liver. Our goal is to use these stem cells as treatment for human liver disease
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    Funded Activity

    Cellular Cross-talk Between Liver Progenitor Cells And Hepatic Stellate Cells Is Required For Hepatic Fibrogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $618,517.00
    Summary
    Deloitte Access Economics data proposes the total economic burden of liver disease in Australia in 2012 was >$50 billion. This study will identify how the liver heals itself by inducing liver cell populations which interact to regenerate damaged liver tissue in chronic liver disease. This knowledge may lead to the development of novel therapeutic interventions for the treatment of liver scarring and liver cancer, and to assist in normal liver regeneration following chronic liver disease.
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    Funded Activity

    Effects Of Caloric Retriction On Age-related Changes In Liver Sinusoidal Endothelial Cell Mitochondria

    Funder
    National Health and Medical Research Council
    Funding Amount
    $8,080.00
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    Funded Activity

    Functional Dyspepsia: Characterisation Of The Immunopathology And Testing A Novel Therapeutic Strategy.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $739,604.00
    Summary
    Dyspepsia, unexplained stomach discomfort and pain, is a common and costly problem; few effective treatments exist and the causes are unknown. We have found that the numbers of a type of immune cell, the eosinophil, are increased in the top of the small bowel in patients with dyspepsia. This study will explore the mechanisms that lead to increased eosinophils and then test the effectiveness of a treatment to suppress this overactive immune response which could rapidly change clinical practice.
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    Funded Activity

    Role Of Hepatic Stellate Cell And Liver Progenitor Cell Interactions In The Regulation Of Wound Healing And Liver Regeneration

    Funder
    National Health and Medical Research Council
    Funding Amount
    $620,716.00
    Summary
    The liver has a remarkable capacity for regeneration following acute and chronic liver injury, however, the mechanisms which facilitate this wound healing are not understood. This project will examine the interactions between different liver cell populations, including hepatic stellate cells (liver fibroblasts) and liver progenitor cells (stem cells of the liver) and will determine which factors regulate inflammation, liver scarring and restitution of liver mass following chronic liver injury.
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    Funded Activity

    Mechanisms Of Hepatic Fibrogenesis In Chronic Liver Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $697,209.00
    Summary
    Despite advances made in understanding the mechanisms of liver injury, chronic liver disease continues to be one of the most rapidly growing causes of death in subjects aged <65 years. This is the result of uncontrolled wound healing and regeneration leading ultimately to cirrhosis and liver cancer. This research will identify and characterise pathways that control the wound healing response to liver injury, involving the processes of inflammation, scarring and restitution of normal liver mas .... Despite advances made in understanding the mechanisms of liver injury, chronic liver disease continues to be one of the most rapidly growing causes of death in subjects aged <65 years. This is the result of uncontrolled wound healing and regeneration leading ultimately to cirrhosis and liver cancer. This research will identify and characterise pathways that control the wound healing response to liver injury, involving the processes of inflammation, scarring and restitution of normal liver mass.
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    Funded Activity

    Understanding And Applying Macrophage-mediated Effects On Liver Progenitor Cells To Treat Liver Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $628,109.00
    Summary
    As liver cancer risk correlates with increased liver stem/progenitor cell numbers, therapies that reduce their numbers will reduce cancer development. On the contrary, therapies to increase progenitor cell numbers will assist their use in cell therapy-based approaches or artificial liver devices to treat chronic liver disease. This project will determine how to use inflammatory cells to manipulate progenitor cell numbers.
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    Funded Activity

    The Liver Sieve And Hyperlipidaemia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $98,116.00
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    Funded Activity

    Defining The Role Of MMP-9-expressing Macrophages In Liver Injury In Chronic Liver Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $542,028.00
    Summary
    Defining pathways that lead to fibrosis in chronic liver disease is an urgent priority and unmet need because cirrhosis remains a major cause of death. We will study the development of an additional fibrogenic pathway involving altered liver repair mechanisms, in order to seek ways to restore liver function. New insights arising from this novel research could significantly advance our understanding of how fibrosis develops and lead to new approaches to treat and prevent advanced liver disease.
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