Brm And Brg-1 Protect From Ultraviolet Radiation-induced Skin And Ocular Damage
Funder
National Health and Medical Research Council
Funding Amount
$555,325.00
Summary
Ultraviolet radiation within sunlight is the most important environmental hazard to which Australians are exposed. It causes cancers of the skin and eye, in addition to other forms of skin and eye damage. However sunlight also has health benefits such as vitamin D production. To protect our health from the sun we need to understand how it causes damage and the meachanisms involved. We have discovered a new pathway that we plan to study, called Brm and Brg-1, that provides protection from UV.
Television Advertising To Promote NHMRC Guidelines For Low Risk Alcohol Consumption: Experimental Study
Funder
National Health and Medical Research Council
Funding Amount
$670,013.00
Summary
This project aims to experimentally assess the impact of television advertising that promotes the 2009 NHMRC Guidelines on alcohol consumption, on adults' (aged 18-64) estimates of drinking levels that incur an increased risk of short and long term harm. The Guidelines advise that adults should limit consumption to 2 standard drinks/day to reduce the risk of lifetime harm, and to 4 standard drinks on any single drinking occasion to reduce the risk of short-term harm from that occasion.
Testing The Imprecision Hypothesis Of Chronic Pain.
Funder
National Health and Medical Research Council
Funding Amount
$788,984.00
Summary
Pain usually occurs when something triggers activity in danger receptors, which are all over the body. The brain receives a huge amount of other sensory input too, which tells the brain what was happening when the danger arose. The brain imprints this sensory barrage and uses it as an early (painful!) warning system next time. If the imprint is imprecise, then the painful warning occurs in non-dangerous situations. We will test whether imprecise imprinting of the sensory input causes the gradual ....Pain usually occurs when something triggers activity in danger receptors, which are all over the body. The brain receives a huge amount of other sensory input too, which tells the brain what was happening when the danger arose. The brain imprints this sensory barrage and uses it as an early (painful!) warning system next time. If the imprint is imprecise, then the painful warning occurs in non-dangerous situations. We will test whether imprecise imprinting of the sensory input causes the gradual development of chronic debilitating pain.Read moreRead less
Rumination And Deficits In The Recall Of Positive Autobiographical Memories In Depression
Funder
National Health and Medical Research Council
Funding Amount
$263,295.00
Summary
The prevalence of depression is increasing and risk of recurrence exceeds 80%. The social and economic burden of depression highlight the urgent need to advance understanding of the habits of thought and memory that keep people feeling depressed, so that psychologists can treat depression more effectively. This project will explain why depressed people feel worse when they recall happy memories. The outcomes will extend theory and guide the improvement of treatments for this condition.
Immune-modifying-particle-induced Tregs Induce Remission In Experimental Autoimmune Encephalomyelitis
Funder
National Health and Medical Research Council
Funding Amount
$512,440.00
Summary
Multiple Sclerosis is a debilitating autoimmune disease of the central nervous system. Disease is the result of inflammatory monocyte-derived dendritic cells that migrate from the blood into the brain, where they stimulate T cells to attack myelin sheaths around neurons. Our novel therapy, known as immune modulating micro-particles reduces monocyte migration and disease in a mouse model, we hypothesize, by inducing immunosuppressive T regulatory cells that control attacking T cells in MS.
Immunotherapeutic Strategies In Anti Myeloperoxidase ANCA Associated Glomerulonephritis
Funder
National Health and Medical Research Council
Funding Amount
$615,998.00
Summary
Kidney disease is the 10th most common cause of death in Australia. Glomerulonephritis (GN) is a major cause of kidney disease. Autoimmunity underpins disease in most patients with the most severe forms. Following the discovery of the peptide that is the target of this autoimmunity promising new biological treatments are possible. This grant will assess the capacity of four emerging therapies to turn off injurious autoimmunity and treat disease.
Intraductal Carcinoma Of The Prostate: Indicator Of Aggressive Disease.
Funder
National Health and Medical Research Council
Funding Amount
$884,377.00
Summary
This proposal addresses the need to improve personalised treatment decisions for men with high risk familial prostate cancer as they have a very aggressive disease progression with a very poor clinical outcome. We will perform biological and pre-clinical studies to improve the clinical diagnosis, prognosis and treatment options for men with germline mutations in BRCA2 or BRCA1 genes who develop prostate cancer.
The Therapeutic Role Of Complement Inhibition In ANCA Associated Glomerulonephritis
Funder
National Health and Medical Research Council
Funding Amount
$600,964.00
Summary
ANCA associated vasculitis is an inflammatory disease involving the kidney filters which is a major cause of chronic kidney failure. Current drugs to treat it are toxic. Less toxic treatments are required. In this study we will explore the potential for new treatments targeting complement (a normal blood protein involved in inflammation) to attenuate this disease in mice. We hope to define the role of complement in this disease and the benefits of inhibiting it before we use it in humans.
Targeting Tregs Using Chimeric Antigen Receptors (CARs) For The Treatment Of Autoimmune Renal Disease
Funder
National Health and Medical Research Council
Funding Amount
$845,519.00
Summary
Chronic Kidney Disease is one of the major causes of death in Australia. Therapeutic success with regulatory T cells (Tregs) capable of targeting autoimmune kidney disease would have major clinical implications. In the proposed study, we will use Chimeric Antigen Receptors (CARs) T cells by redirecting them to diseased organs, protect against kidney injury. These CAR T cells will recognise renal antigens and target immune cells and antibodies to limit kidney damage.
TDP-43 In The Population In Relation To Dementia: Relationships With Clinical Symptomatology And Other Key Neuropathologies
Funder
National Health and Medical Research Council
Funding Amount
$235,002.00
Summary
There are over a quarter of a million people with dementia in Australia, and this figure will rise. We still do not understand what goes wrong within the brain to give rise to dementia. This project will assess a new pathology within the brain in relation to late life dementia and the aging process. Results will improve diagnostic tools for dementia and treatments.