Immunological Prevention Of Cysticercosis And Hydatid Disease
Funder
National Health and Medical Research Council
Funding Amount
$567,868.00
Summary
Cysticercosis and hydatid disease are caused by infections with the larval stages of tapeworm parasites. They are life-threatening zoonotic diseases, transmitted to humans from animals and are most common in people living in poor countries. This project aims to develop practical vaccines to assist with the prevention of these diseases in humans. We will vaccinate the parasites' natural animal hosts and break the parasite life-cycles, thereby indirectly and inexpensively preventing the diseases b ....Cysticercosis and hydatid disease are caused by infections with the larval stages of tapeworm parasites. They are life-threatening zoonotic diseases, transmitted to humans from animals and are most common in people living in poor countries. This project aims to develop practical vaccines to assist with the prevention of these diseases in humans. We will vaccinate the parasites' natural animal hosts and break the parasite life-cycles, thereby indirectly and inexpensively preventing the diseases being passed to humans.Read moreRead less
A Novel Approach To Identify The Specific Antibody Characteristics Important For Protection From Malaria In Pregnant Women
Funder
National Health and Medical Research Council
Funding Amount
$1,011,223.00
Summary
Antibody protects against malaria, but the specific characteristics of protective antibody are unknown. Pregnant women lack antibody to parasite protein called VAR2CSA, explaining their malaria susceptibility. Using samples from vaccine trials and clinical studies in pregnant women, and a ‘Systems Serology’ approach, we will determine which naturally-acquired or vaccine induced antibodies protect pregnant women from malaria, and how variation in VAR2CSA sequences affects this protection.
Secreted Exosome-like Vesicles From The Carcinogenic Liver Fluke
Funder
National Health and Medical Research Council
Funding Amount
$771,543.00
Summary
Parasitic liver flukes secrete microscopic cell-like vesicles into the bile ducts when feeding on infected humans. These vesicles, called exosomes, are taken up by the cells lining the bile ducts and promote them to become pre-cancerous. We will characterise the contents of these fluke exosomes and identify the key molecules on their surfaces that can be used to prevent exosome uptake by cells and ultimately form the basis of a vaccine that prevents fluke infection and subsequent liver cancer.
Surface Antigens Of Plasmodium Falciparum-infected Erythrocytes And Immunity To Malaria In Humans
Funder
National Health and Medical Research Council
Funding Amount
$599,180.00
Summary
Malaria is a leading cause of death globally, particularly among children. Malaria parasites infect red blood cells and multiply inside them, resulting in severe illness if left untreated. Effective treatments are limited and currently there is no vaccine. In human studies, we aim to identify the target antigens of immune responses and immune mechanisms that protect against malaria. With this knowledge, vaccines can be designed against malaria to prevent serious illness and death.
A Transmission-Blocking Vaccine To Prevent Toxoplasmosis
Funder
National Health and Medical Research Council
Funding Amount
$850,225.00
Summary
Toxoplasma gondii causes a globally important zoonotic disease. It is transmitted by cats, and finds its way into our food chain via infected meat and contaminated water. We have used a unique functional genomics pipeline to discover proteins crucial for reproduction of Toxoplasma in the cat. We will now test combinations of these proteins to immunise cats and prove that we can develop a vaccine that blocks transmission of this highly significant parasitic disease.
Mechanisms And Targets Of Antibody-complement Interactions That Neutralize Malaria
Funder
National Health and Medical Research Council
Funding Amount
$647,977.00
Summary
Our project aims to identify immune mechanisms that neutralize malaria from the moment of inoculation by a mosquito, before infection can become established to prevent the development of malaria disease. Furthermore, we will discover specific targets of protective immune responses. We expect this project will provide major new advances in our knowledge of human immunity to P. falciparum malaria, one of the world’s most significant causes of mortality and morbidity, and we will use this knowledge
Plasmodium vivax is a parasite that invades the youngest of human red blood cells. Our work will reveal how this malaria parasite enters our blood cells and the molecular mechanisms that allows successful invasion. This proposal will redefine our understanding of P. vivax invasion and explore novel ways to block its entry into red blood cells and therefore prevent malaria infection.
Export Of PfEMP1, The Major Virulence Protein Of P. Falciparum, To The Parasite-infected Erythrocyte Surface
Funder
National Health and Medical Research Council
Funding Amount
$588,532.00
Summary
The malaria parasite infects red blood cells in the human host and initiates major remodelling. This involves export of a major virulence protein to the surface of the red blood cell. This research seeks to understand how the parasite exports this protein, a key determinant of disease.
Functional Assays Of Immunity To Malaria In Pregnant Women
Funder
National Health and Medical Research Council
Funding Amount
$578,905.00
Summary
Pregnant women are highly susceptible to malaria due to the adhesion of infected erythrocytes to the placenta. Antibodies to these infected erythrocytes can block their placental adhesion and/or facilitate their clearance by immune cells, improving pregnancy outcomes. We aim at informing vaccine design by better understanding the placental adhesion mechanisms and identifying targets of protective immunity as well as antibody correlates of protection from placental malaria and its consequences.
Schistosomiasis is a major public health problem in the Philippines with approximately 6.7 million people at risk of infection. Mass human chemotherapy has formed the cornerstone of control for decades but has failed to control the disease. Transmission reduction is a key step towards elimination and integrated interventions should target both definitive and intermediate host transmission pathways. We propose to trial integrated control strategies for the disease and expect the outcomes to have ....Schistosomiasis is a major public health problem in the Philippines with approximately 6.7 million people at risk of infection. Mass human chemotherapy has formed the cornerstone of control for decades but has failed to control the disease. Transmission reduction is a key step towards elimination and integrated interventions should target both definitive and intermediate host transmission pathways. We propose to trial integrated control strategies for the disease and expect the outcomes to have broader implications for Southeast Asia.Read moreRead less