Control Of The Antigen-specific Cytotoxic T Cell Memory Response
Funder
National Health and Medical Research Council
Funding Amount
$95,044.00
Summary
Individuals who survive infections by a given pathogenic micro-organism are usually protected from subsequent infections by these same agents. This is the basis of adaptive immunity, which defines the body's ability to maintain a memory of prior infection or vaccination and in so doing, mount a far more effective response to subsequent infection by these agents. This proposal deals with the mechanisms by which this memory is maintained. It specifically focuses on cytotoxic T lymphocytes (CTL) wh ....Individuals who survive infections by a given pathogenic micro-organism are usually protected from subsequent infections by these same agents. This is the basis of adaptive immunity, which defines the body's ability to maintain a memory of prior infection or vaccination and in so doing, mount a far more effective response to subsequent infection by these agents. This proposal deals with the mechanisms by which this memory is maintained. It specifically focuses on cytotoxic T lymphocytes (CTL) which are leucocytes or white blood cells that kill virus infected cells. Using new technology which permits visualisation of CTL directed against specific viruses we are going to define what determines the survival and replacement of these memory cells over time. We will also identify the agents that alter the memory CTL's ability to deal with infections within localised sites in the body. In so doing, this work will provide valuable insight into approaches that can be used to better vaccinate individuals against infections by pathogenic viruses.Read moreRead less
Mechanisms Of Macrophage Activation By Immunostimulatory DNA
Funder
National Health and Medical Research Council
Funding Amount
$230,728.00
Summary
This project is based upon the observation that the mammalian immune system can distinguish between its own genetic material (DNA) and the genes of infectious agents such as bacteria. This fact has implications for understanding how the immune system copes with infection, and also for design of new therapies and vaccines. Our central aim is to define exactly how this recognition system works. The cells that respond most vigorously to foreign DNA are large white blood cells called macrophages. We ....This project is based upon the observation that the mammalian immune system can distinguish between its own genetic material (DNA) and the genes of infectious agents such as bacteria. This fact has implications for understanding how the immune system copes with infection, and also for design of new therapies and vaccines. Our central aim is to define exactly how this recognition system works. The cells that respond most vigorously to foreign DNA are large white blood cells called macrophages. We aim to find the macrophage protein which binds to foreign DNA and triggers the activation of the immune system. The type of immune responses initiated by foreign DNA may be useful in treatment of allergies and cancer and for improving vaccinations.Read moreRead less
Regulation Of Natural Killer Cell Homeostasis By Multiple Components Of The Immune System
Funder
National Health and Medical Research Council
Funding Amount
$327,151.00
Summary
Differentiation and homeostasis of immune cell populations such as CD4 and CD8 T cells and dendritic cells has been key to understanding their function during inflammation. In contrast, late stage natural killer (NK) cell differentiation has largely been ignored. Given the key role of NK cells in providing innate effector immunity and shaping adaptive responses, a better understanding of the cues that regulate their differentiation is clearly warranted.