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Research Topic : T Cell Immunity
Scheme : Project Grants
Australian State/Territory : ACT
Status : Closed
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Medical Virology (4)
Cellular Immunology (2)
Medical Parasitology (2)
Allergy (1)
Autoimmunity (1)
Biochemistry and Cell Biology not elsewhere classified (1)
Epigenetics (incl. Genome Methylation and Epigenomics) (1)
Signal Transduction (1)
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  • Funded Activities (13)
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  • Funded Activity

    How Does NF-kB2 Regulate Thymic Selection To Prevent Organ-specific Autoimmune Disease?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $787,600.00
    Summary
    Autoimmune diseases like type 1 diabetes and thyroiditis arise from defects that cause the immune system to confuse self and non-self. Normally, this distinction is programmed in the thymus. We recently identified the gene that causes a form of autoimmune disease. We also made an important discovery about how the thymus gland regulates self-non-self discrimination. We will build on these two discoveries to gain a precise understanding of how the immune system normally avoids autoimmune disease.
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    Funded Activity

    Modeling Human Actin Related Protein 2/3 Complex Subunit 1B (ARPC1B) Deficiency In Mice

    Funder
    National Health and Medical Research Council
    Funding Amount
    $755,005.00
    Summary
    The actin cytoskeleton forms the structure that not only keeps cells in their normal shape but is also essential for the movement of cells and for interaction between cells. We have recently identified the first patients with an immunodeficiency caused by a defect in a gene called ARPC1B, which plays a crucial role in the regulation of actin. Through the investigation of novel mouse models we will elucidate the pathomechanism underlying the disease of these patients.
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    Funded Activity

    Genomic Medicine For Human Immune Deficiency

    Funder
    National Health and Medical Research Council
    Funding Amount
    $535,495.00
    Summary
    It is feasible to sequence patient genomes but we need to know more about how genetic variants cause complex disease. We have sequenced genomes from patients with immune deficiency and will test the idea that genetic variation causes consistent changes in particular white blood cells, thus providing a bridge between genomic information and clinical diagnosis. Outcomes will include more accurate diagnosis, better understanding of immunity, and a strategy for using whole genome information.
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    Funded Activity

    The Role Of Duffy And PF4 In The Platelet Killing Of Malaria Parasites.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $350,045.00
    Summary
    Platelets in the blood can kill the Plasmodium parasite, which lives inside red blood cells and causes malaria. Platelets bind parasite-infected red cells and release a molecule that is toxic to the parasite. This project will study why a red cell molecule called Duffy is also needed for this function of platelets. Most Africans carry a gene for Duffy that stops its expression in red cells, and may therefore be more susceptible to malaria because their platelets cannot kill the malaria parasite.
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    Funded Activity

    Methylation-sensitive T Cell Genes And Childhood Food Allergy.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $461,232.00
    Summary
    Australia has the highest reported prevalence food allergy in the world. Despite this, little is known about how allergy develops. Mounting evidence implicates environmentally induced disruption of the genetic blueprint via a process known as epigenetics. We are combining the strengths of food challenge proven food allergy with assessment of immune functioning & cutting edge genomics, to extensively characterise the pathways leading to food allergy in children.
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    Funded Activity

    Methylation Sensitive Genes And The Transition To Allergic Disease: A Twin Study

    Funder
    National Health and Medical Research Council
    Funding Amount
    $493,843.00
    Summary
    Australia has amongst the highest reported prevalence allergic conditions (including asthma) in the world. Despite this, little is known about how these conditions arise. Mounting evidence implicates environmentally induced disruption of the genetic blueprint via a process known as epigenetics. We are combining the strengths of a unique collection of identical twins where one of a pair is sensitive to house dust mite, with cutting edge genomics, to characterise the pathways leading to allergy in .... Australia has amongst the highest reported prevalence allergic conditions (including asthma) in the world. Despite this, little is known about how these conditions arise. Mounting evidence implicates environmentally induced disruption of the genetic blueprint via a process known as epigenetics. We are combining the strengths of a unique collection of identical twins where one of a pair is sensitive to house dust mite, with cutting edge genomics, to characterise the pathways leading to allergy in children.
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    Funded Activity

    Arbovirus Activation And Modulation Of NLRP3 Inflammasome

    Funder
    National Health and Medical Research Council
    Funding Amount
    $779,720.00
    Summary
    This project aims to establish how mosquito borne viruses such as Ross River and dengue viruses interacts with the human host to cause disease, including how the virus evades the host’s immune response to persist and cause disease for prolonged periods. Knowing how differences in the virus and the host’s immune system interplay to cause asymptomatic to severely disabling disease will assist in devising new treatments and prevention programs to lessen the impact of these diseases in Australia.
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    Funded Activity

    Spatio-temporal Dynamics Of Arbovirus Infection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $491,504.00
    Summary
    Mosquito-borne alphaviruses such as Ross River and chikungunya viruses cause widespread epidemics and exert extreme pressure on the public health systems of affected regions. Alphaviruses spreads to joints and triggers a severe disease in those affected. There are no effective treatments or vaccines. The project will investigate virus-host interaction at the bite site. The outcome will be new knowledge to treat infection at the mosquito bite site to prevent joint disease.
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    Funded Activity

    Novel Insights Into The Pathobiology Of Alphavirus Infections

    Funder
    National Health and Medical Research Council
    Funding Amount
    $827,660.00
    Summary
    Infections with mosquito-borne viruses are increasing at an alarming rate worldwide. Ross River virus is endemic in parts of Australia, PNG and Pacific islands, while chikungunya virus is distributed globally and causes recurrent pandemics that involve millions of people. These viruses cause severe musculoskeletal disease for several months after infection. This project aims to establish how these viruses interact with the human host to cause disease and may provide a basis for new treatments.
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    Funded Activity

    Inhibition Of Interferon-?/? Induction By Ross River Virus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $589,664.00
    Summary
    Ross River virus is a mosquito-borne virus that causes arthritis in the joints of many people infected. This project will look at the early interactions of a virulent virus with the mammalian host that appear to enable the virus to replicate and spread in the host and thereby cause disease. These interactions are with the host interferon protein which the virus has developed the ability to inhibit. The effect of the invading virus on the host's interferon system, part of the immune system, will .... Ross River virus is a mosquito-borne virus that causes arthritis in the joints of many people infected. This project will look at the early interactions of a virulent virus with the mammalian host that appear to enable the virus to replicate and spread in the host and thereby cause disease. These interactions are with the host interferon protein which the virus has developed the ability to inhibit. The effect of the invading virus on the host's interferon system, part of the immune system, will be examined.
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    Showing 1-10 of 13 Funded Activites

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