Immunoregulation Of Subsets Of Memory CD8+ T Cells
Funder
National Health and Medical Research Council
Funding Amount
$233,867.00
Summary
Information will be sought on the properties of T cells, a class of white blood cells that play a vital role in combating infectious agents. Using mouse models, subsets of T cells that carry immunological memory will be studied and assessed for their rate of cell division and dependence on soluble messengers known as cytokines and other stimuli. The data will provide useful knowledge on the causes of autoimmune diseases (such as rheumatoid arthritis, type 1 diabetes and lupus) and help in the de ....Information will be sought on the properties of T cells, a class of white blood cells that play a vital role in combating infectious agents. Using mouse models, subsets of T cells that carry immunological memory will be studied and assessed for their rate of cell division and dependence on soluble messengers known as cytokines and other stimuli. The data will provide useful knowledge on the causes of autoimmune diseases (such as rheumatoid arthritis, type 1 diabetes and lupus) and help in the development of successful second generation vaccines.Read moreRead less
The Generation Of HSV-1 Specific Effector And Memory CD4+ T Cell Responses.
Funder
National Health and Medical Research Council
Funding Amount
$460,509.00
Summary
This proposal aims to determine the mechanisms underpinning the generation of helper T cell responses following HSV-1 infection. It will determine the factors that allow T cells to access sites of viral replication and the mechanisms by which they provide protection from skin infections.
Investigating The Role Of TGF-beta In Resident Memory T Cell Induction And Maintenance
Funder
National Health and Medical Research Council
Funding Amount
$92,495.00
Summary
I am a research scientist interested in the immune system. Specifically, I intend to investigate immunological memory, which is the basis of vaccination. This refers to the ability of certain immune cells such as T and B cells to ‘remember’ a pathogen, so that a rapid and enhanced response can be generated upon re-infection with the same pathogen. This can be investigated by experimental techniques such as flow cytometry, histology and confocal microscopy on cells from infected mouse tissue.
Epigenetic Regulation Of CD8+ T Cell Function And Memory.
Funder
National Health and Medical Research Council
Funding Amount
$578,171.00
Summary
Upon virus infection, a subset of white blood cells, called killer T cells, are recruited to fight the infection. This proposal aims to examine molecular changes that occur within killer T cells and impart their specific function. We also aim to understand how killer T cells are _programmed� as they establish immunological memory. This proposal will provide insights important for the design and improvement of vaccine strategies to fight pathogens such as influenza, HIV and even tumors.
Effector And Memory CD8+ T Cell Responses To Engineered Influenza A Escape Mutants
Funder
National Health and Medical Research Council
Funding Amount
$465,210.00
Summary
T cells are a critical component of the immune system after infection with viruses. In particular, virus-specific CD8+ T cells can clear viral infections by killing virally-infected cells and the release of immunomodulators. These are called effector T cells. After the viral infection is cleared, a small proportion of T cells (around 5 to 10%) survives for many years and constitute a memory pool of virus-specific T cells. Memory T cells provide a rapid and effective protection in case of a repea ....T cells are a critical component of the immune system after infection with viruses. In particular, virus-specific CD8+ T cells can clear viral infections by killing virally-infected cells and the release of immunomodulators. These are called effector T cells. After the viral infection is cleared, a small proportion of T cells (around 5 to 10%) survives for many years and constitute a memory pool of virus-specific T cells. Memory T cells provide a rapid and effective protection in case of a repeated infection with the same virus, and hence result in a less severe disease. However, viruses often mutate their genes to escape such efficient T cell responses. In this study, we will investigate T cell responses after infection with mutated strains of influenza viruses. We will engineer a panel of mutant influenza viruses, which alter the nature and characteristics of T cells. We will analyse how efficient are these T cells and whether they can protect against a normal strain of influenza A. Subsequently, we will characterise quantitative and qualitative aspects of memory T cell pools after infection with mutant influenza viruses. Since a number of viruses such as influenza, HIV and HCV rapidly mutate their genes, our study will not only address the question of T cell responses to mutated influenza viruses, but also will provide an excellent model for investigating protective T cell responses to other viral infections.Read moreRead less
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
Delineating Aberrant Adaptive Immune Responses Due To Germline Mutations In The PI3K Signalling Pathway
Funder
National Health and Medical Research Council
Funding Amount
$975,476.00
Summary
Activation of immune cells is required to generate appropriate immune responses that protect is from disease caused by pathogens. The inability to receive the correct type of signals causes immunodeficiency. The PI3 kinase pathway is central to immune cell activation – and genetic errors in this pathwat compromise the functioning of immune cells. We will investigate the nature of these defects and pursue avenues of overcoming them using pharmacological inhibitors of the PI3K pathway.