How the immune system recognises vitamin B-based allergies. This project aims to evaluate the range of molecules that can stimulate vitamin B-reactive T cells in mammals and amphibians, and the degree of conservation or variation in these molecules among diverse microorganisms. T cells are immune cells that recognise foreign molecules, including peptides, lipids and vitamin B metabolites, bound to specialised antigen-presenting molecules. In mammals, Mucosal Associated Invariant T cells, still p ....How the immune system recognises vitamin B-based allergies. This project aims to evaluate the range of molecules that can stimulate vitamin B-reactive T cells in mammals and amphibians, and the degree of conservation or variation in these molecules among diverse microorganisms. T cells are immune cells that recognise foreign molecules, including peptides, lipids and vitamin B metabolites, bound to specialised antigen-presenting molecules. In mammals, Mucosal Associated Invariant T cells, still poorly understood, recognise Vitamin B-based molecules. Combining immunology with structural biology and chemistry, this project aims to understand how the immune system detects molecules produced by diverse microorganisms.Read moreRead less
Whole-body analysis of human tissue-resident memory T cells. T cells provide critical immune protection against infection and cancer, and dysfunctional T cells cause autoimmune disease. Much of our understanding of T cells comes from studies of mice and how these immune cells work in humans is not fully understood. This project aims to determine how human T cells persist and function using a unique organ donor tissue resource. The expected outcomes are to generate fundamental new knowledge about ....Whole-body analysis of human tissue-resident memory T cells. T cells provide critical immune protection against infection and cancer, and dysfunctional T cells cause autoimmune disease. Much of our understanding of T cells comes from studies of mice and how these immune cells work in humans is not fully understood. This project aims to determine how human T cells persist and function using a unique organ donor tissue resource. The expected outcomes are to generate fundamental new knowledge about the regulation of the human immune response. This knowledge is critical for the development of vaccines and immunotherapies designed to harness T cell immunity.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE200100292
Funder
Australian Research Council
Funding Amount
$426,018.00
Summary
Defining the basis of unconventional immune cell development. This project aims to undertake discovery research to characterise the transcriptional programs that underpin the development of unconventional immune cells. This project expects to generate new knowledge in the area of developmental immunology by using cutting-edge molecular and cellular techniques to examine the seeding of immune cells. It is expected that this project will advance our understanding of immune cell biology and the pro ....Defining the basis of unconventional immune cell development. This project aims to undertake discovery research to characterise the transcriptional programs that underpin the development of unconventional immune cells. This project expects to generate new knowledge in the area of developmental immunology by using cutting-edge molecular and cellular techniques to examine the seeding of immune cells. It is expected that this project will advance our understanding of immune cell biology and the programs that control them. Significantly strengthening national excellence in unconventional immune cell research and providing innovative methodology. This should provide significant benefits, such as a comprehensive open-access transcriptional map of developing unconventional immune cells.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE170100407
Funder
Australian Research Council
Funding Amount
$372,000.00
Summary
Biology of immune cells. This project aims to study immune cells that target harmful microbes by recognising by-products of their metabolism, and develop methods modulating their function. In particular, it aims to determine the immune recognition of the full range of microbial metabolites that activate these cells and unravel the mechanisms behind tolerance to nutrition-derived metabolites. This project is a potential opportunity for Australia to maximise its competitive edge in this field and ....Biology of immune cells. This project aims to study immune cells that target harmful microbes by recognising by-products of their metabolism, and develop methods modulating their function. In particular, it aims to determine the immune recognition of the full range of microbial metabolites that activate these cells and unravel the mechanisms behind tolerance to nutrition-derived metabolites. This project is a potential opportunity for Australia to maximise its competitive edge in this field and develop immune-modulatory agents ultimately leading to socioeconomic benefit.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE180100484
Funder
Australian Research Council
Funding Amount
$365,058.00
Summary
Tipping the balance from tolerance to immunity for the devil facial tumour. This project aims to develop a single-shot vaccine for the Tasmanian devil facial tumour disease. The disease is an enigma because the transmissible tumours are simultaneously cancer, infections, and genetically mismatched tissue grafts. This project will focus on immune molecules that are revolutionising human oncology, and will develop techniques to understand and systematically test the function of these key molecules ....Tipping the balance from tolerance to immunity for the devil facial tumour. This project aims to develop a single-shot vaccine for the Tasmanian devil facial tumour disease. The disease is an enigma because the transmissible tumours are simultaneously cancer, infections, and genetically mismatched tissue grafts. This project will focus on immune molecules that are revolutionising human oncology, and will develop techniques to understand and systematically test the function of these key molecules in Tasmanian devils. Understanding the role of these immune molecules will accelerate development of a vaccine to help save the devil and has the potential to shed light on general principles relating to how the immune system balances tolerance and immunity.Read moreRead less
Immunisation to protect against transmissible cancers in Tasmanian devils. This project aims to identify the immune escape mechanisms that the transmissible cancers, Devil Facial Tumour Disease (DFTD) use to avoid being killed by the immune system. Since the discovery of the second transmissible cancer (DFT2) mystery surrounds whether the devils immune system can respond to this cancer, hence this project will investigate the immune response to DFT2. The final aims are to develop a vaccine with ....Immunisation to protect against transmissible cancers in Tasmanian devils. This project aims to identify the immune escape mechanisms that the transmissible cancers, Devil Facial Tumour Disease (DFTD) use to avoid being killed by the immune system. Since the discovery of the second transmissible cancer (DFT2) mystery surrounds whether the devils immune system can respond to this cancer, hence this project will investigate the immune response to DFT2. The final aims are to develop a vaccine with the potential to protect healthy devils and cure devils with DFTD.Read moreRead less
Histone deacetylase functions in immune cells. This project aims to define how an enzyme (a histone deacetylase) enables innate immune cells (macrophages) to respond to specific danger signals, such as those activating Toll-like Receptors. To identify processes that provide specificity to signal transduction pathways, this project will characterise protein targets and biological functions of a specific class IIa histone deacetylase in macrophages. This project expects to result in an understandi ....Histone deacetylase functions in immune cells. This project aims to define how an enzyme (a histone deacetylase) enables innate immune cells (macrophages) to respond to specific danger signals, such as those activating Toll-like Receptors. To identify processes that provide specificity to signal transduction pathways, this project will characterise protein targets and biological functions of a specific class IIa histone deacetylase in macrophages. This project expects to result in an understanding of histone deacetylases and protein deacetylation in immune cell responses which can be harnessed to manipulate cell functions for basic science and biotechnology uses.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE140100432
Funder
Australian Research Council
Funding Amount
$394,308.00
Summary
Defining the mechanisms of tissue-resident memory T cell development. We have recently identified a subset of T cells that reside at points of pathogen entry where they can effectively control infection. The ability of these T cells to offer local immunity has caused a paradigm shift in our view of how T cells protect against infection, drastically changing the way we think about designing T cell vaccines. This project aims to characterise this novel T cell subset, defining the fundamental requi ....Defining the mechanisms of tissue-resident memory T cell development. We have recently identified a subset of T cells that reside at points of pathogen entry where they can effectively control infection. The ability of these T cells to offer local immunity has caused a paradigm shift in our view of how T cells protect against infection, drastically changing the way we think about designing T cell vaccines. This project aims to characterise this novel T cell subset, defining the fundamental requirements for their formation and maintenance. This will lead to a greater understanding of their biology, which will be of significance for the development of novel vaccination strategies.Read moreRead less
Understanding the diverse biology of CD4+ T cell resident memory. This project aims to examine the biology of CD4 T cell memory in tissues. The previously unappreciated complexity of the CD4 T cell resident memory compartment in the liver will be characterised, focusing on the generation, maintenance and diversity of functions of these cells. Expected outcomes include the generation of fundamental knowledge in the disciplines of cellular biology and immunology, and unique, highly specialised stu ....Understanding the diverse biology of CD4+ T cell resident memory. This project aims to examine the biology of CD4 T cell memory in tissues. The previously unappreciated complexity of the CD4 T cell resident memory compartment in the liver will be characterised, focusing on the generation, maintenance and diversity of functions of these cells. Expected outcomes include the generation of fundamental knowledge in the disciplines of cellular biology and immunology, and unique, highly specialised student and personnel training through the interdisciplinary approach utilised, which spans cellular biology, live-imaging and transcriptomic analyses. Expected benefits include influential publications and the import of a novel, specialised technique to Australia through an international collaboration (Germany)Read moreRead less
Antigen selection mechanisms control T cell immunity against bacteria. CD4+ T (T helper) cells are required to control many important bacterial infections. This Project aims to identify the key targets of CD4+ T cells responding to a model bacterial infection, and to correlate potential antigen effectiveness with native expression, antigen presentation, and the function of antigen-specific CD4+ T cells over time. Our validated experimental 'pipeline' has unprecedented potential to define potent ....Antigen selection mechanisms control T cell immunity against bacteria. CD4+ T (T helper) cells are required to control many important bacterial infections. This Project aims to identify the key targets of CD4+ T cells responding to a model bacterial infection, and to correlate potential antigen effectiveness with native expression, antigen presentation, and the function of antigen-specific CD4+ T cells over time. Our validated experimental 'pipeline' has unprecedented potential to define potent CD4+ T cell antigens within the thousands of proteins expressed by a bacterial pathogen. Our unbiased analysis may help establish the rules that define effective antigenicity. Our work will improve the understanding of bacterial immunity, and inform future design of T-cell based vaccines in the agricultural sector.Read moreRead less