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Research Topic : liver microcirculation
Australian State/Territory : NSW
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Immunology not elsewhere classified (2)
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  • Funded Activity

    Unraveling Mechanisms Of Liver Transplant Tolerance

    Funder
    National Health and Medical Research Council
    Funding Amount
    $694,822.00
    Summary
    Liver transplants are unique amongst solid organs as they are spontaneously accepted across different individuals and induce acceptance of other organs from the same donor co-transplanted at the same time. Using a new mouse liver transplantation model, this proposal will elucidate how the liver tissue performs this function and identify new markers associated with tolerance in the blood of mice. This knowledge will be used to identify liver transplant patients with reduced rejection risk.
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    Funded Activity

    Deciphering Mechanisms Of Liver Allograft Tolerance

    Funder
    National Health and Medical Research Council
    Funding Amount
    $520,964.00
    Summary
    The liver has paradoxical properties: it is the site of effective immune responses to pathogens, but under some circumstances, it is known to induce harmless immune responses. Liver transplants are more readily accepted than other organ grafts in the absence of immunosuppressive drugs but little is known about the mechanisms that prevent an effective response. This proposal aims to unravel these mechanisms. This project will have important implications for transplantation studies.
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    Funded Activity

    Deciphering How TCR Affinity Regulates CD4 T Cell Help In Immunity And Autoimmunity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $850,885.00
    Summary
    Immune responses require the coordinated interaction and cross-talk between two types of white blood cells known as CD4 and CD8 T cells. A dysregulated interaction between these cells could be the cause of autoimmune and persistent infections by pathogens leading to chronic diseases. The aim of this proposal is to provide a deeper understanding of CD4/CD8 T cell interactions to improve immune outcomes in many chronic diseases in which interaction between these two immune cells is critical.
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    Funded Activity

    A Unique Network Of Phagocytic Cells At The Interface Between The Liver And Peritoneal Cavity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $787,521.00
    Summary
    This project aims to characterise the nature and ontogeny of a novel population of cells with phagocytic capacity that forms a network underlying the capsule of mouse and human liver reminiscent of that formed by Langherans cells in the epidermis of the skin. In this project we will characterise this newly described liver capsular macrophage subset, define their ontogeny and assess their specific functions.
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    Funded Activity

    Inflammatory Mediators Of Liver Injury In Chronic Hepatitis C

    Funder
    National Health and Medical Research Council
    Funding Amount
    $349,336.00
    Summary
    Presently, liver disease from chronic hepatitis C and obesity represents a major health problem. Overall, approximately 50% of Australians with chronic hepatitis C are obese and these patients are at significantly increased risk of rapidly progressing to liver failure. It is now recognized that fat derived factors play an important role in regulating inflammatory responses. This grant proposal aims to gain insight into how liver and fat derived inflammatory factors interact to promote increased .... Presently, liver disease from chronic hepatitis C and obesity represents a major health problem. Overall, approximately 50% of Australians with chronic hepatitis C are obese and these patients are at significantly increased risk of rapidly progressing to liver failure. It is now recognized that fat derived factors play an important role in regulating inflammatory responses. This grant proposal aims to gain insight into how liver and fat derived inflammatory factors interact to promote increased liver damage in chronic hepatitis C and obesity.
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    Funded Activity

    Protecting Against Malaria Through Liver-resident Memory T Cells

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,196,853.00
    Summary
    We have shown that formation of liver-resident memory T cells (Trm), a newly discovered type of immune cells, can be induced by an innovative vaccination strategy called prime and trap for highly efficient protection against malaria in mice. Here, we will enhance prime and trap vaccination efficacy by defining the conditions that maximize liver Trm-mediated protection and will characterize simian and human liver Trm cells, paving the way to create the most efficient human malaria vaccine to date
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    Funded Activity

    Immunopathogenesis And Differential Gene Expression Of Hepatitis C Virus Post Liver Transplantation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $69,147.00
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    Funded Activity

    The Unique Nature Of Gamma Delta T Cell Recognition Resolved Through Interaction With H2-Q10

    Funder
    National Health and Medical Research Council
    Funding Amount
    $699,031.00
    Summary
    The liver is important for both digestion and immunity. Given these opposing functions, the liver must exert control points that prevent the immune system from recognising food products. We have now identified a new molecular target that controls the development of immune cells in the liver.
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    Funded Activity

    Imaging The Hepatitis C Virus Life Cycle In Real-time

    Funder
    National Health and Medical Research Council
    Funding Amount
    $477,504.00
    Summary
    Hepatitis C virus (HCV) is a serious viral pathogen that causes significant liver disease. This proposal plans to examine how two proteins from the HCV, core and NS5A, interact with host proteins and pathways to facilitate viral replication and release of HCV; two processes that are poorly understood. Specifically we will tag viral proteins to allow us to investigate the HCV life cycle in living cells and determine the role of core and NS5A in facilitating HCV replication. This proposal may unco .... Hepatitis C virus (HCV) is a serious viral pathogen that causes significant liver disease. This proposal plans to examine how two proteins from the HCV, core and NS5A, interact with host proteins and pathways to facilitate viral replication and release of HCV; two processes that are poorly understood. Specifically we will tag viral proteins to allow us to investigate the HCV life cycle in living cells and determine the role of core and NS5A in facilitating HCV replication. This proposal may uncover novel therapeutic strategies to combat HCV.
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    Showing 1-9 of 9 Funded Activites

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