精东传媒

Funding boost for research to treat Friedreich’s ataxia

Funding boost for research to treat Friedreich’s ataxia

UOW Associate Professor Mirella Dottori leads research into stem-cell therapy

Associate Professor , from the 精东传媒 of 精东传媒 (UOW), has been awarded close to $1 million in research funding from the Medical Research Future Fund for a project that will use human stem cells to develop a curative treatment for Friedreich鈥檚 ataxia (FA).

Associate Professor Dottori, a researcher in the School of Medicine, affiliated with and the  (IHMRI), is the chief investigator on the project and will receive $982,861 over three years from the  (MRFF) and National Health and Medical Research Council (NHMRC) for her ground-breaking research.

Friedreich鈥檚 ataxia is a rare genetically inherited disease that causes degeneration within the nervous system and heart tissue. FA affects hundreds of Australians. There is currently no cure for FA and options to treat symptoms are limited.

Associate Professor Dottori has spent almost 20 years researching disease modelling through stem cells, including more than 10 years focusing specifically on research into FA.

鈥淭he cause of FA is mutations in a gene called Frataxin, which plays an important role in maintaining cell health. Individuals suffering from FA don鈥檛 make enough Frataxin protein in their body, which impacts many tissues, particularly within the nervous system and heart,鈥 Associate Professor Dottori said.

Gene therapy is opening doors to treatments for previously untreatable diseases, and is currently at the forefront as a potential approach to successfully treat this rare genetic disease. The research being led by Associate Professor Dottori is a world-first approach to significantly advance current technologies in gene therapy to treat FA.

鈥淭his research is using stem cells as a platform to develop an optimal gene therapy approach to treat FA,鈥 Associate Professor Dottori said.

鈥淕ene therapy uses genetically modified and very safe viruses to deliver genes, proteins or drugs to the body as a therapy. There are many different viruses that can be used for gene therapy, but each virus targets different tissues with varying efficiencies.

鈥淲e will use stem cells derived from FA patients to make nerves and heart cells 鈥榠n the dish鈥, which will be used to screen different and novel gene therapy viruses to determine the optimal virus for delivering Frataxin protein to the nervous system and heart tissues.鈥 Associate Professor Mirella Dottori said.

The grant is a team effort, led by Associate Professor Dottori in 精东传媒, it includes collaborators from the Children's Medical Research Institute at Westmead Hospital, Sydney, the Murdoch Children鈥檚 Research Institute and St Vincent's Institute of Medical Research in Melbourne, the 精东传媒 of Melbourne and The Council of the Queensland Institute of Medical Research.

鈥淭his grant is the pinnacle of years of work from all of us bringing together our technologies and expertise to develop and deliver a potential curative therapy for FA,鈥 Associate Professor Dottori said.

While gene therapy clinical trials for treating FA are starting in the USA, the research team believe there are more efficient ways to do this utilising new technology, making treatments more specific and preserving other tissues during treatment - including the liver.

鈥淭he current viruses being used in these trials have certain limitations, particularly in terms of tissue targeting. We believe that our platform and technologies can address these limitations and identify novel gene therapy viruses that will deliver more optimal outcomes for FA.鈥 Associate Professor Dottori said.

鈥淥ur aim is to develop an optimal gene therapy approach within the next 3 years, which will then be at the doorstep for clinical trials.鈥

Professor Jennifer L Martin, UOW Deputy Vice-Chancellor (Research and Innovation), congratulated Associate Professor Dottori on receiving the grant.

鈥淚 am thrilled for Associate Professor Dottori and the broader research team. The award of this highly competitive Stem Cell Therapies Mission grant funding is testament to the quality of the interdisciplinary research, and to the impact the research outcomes will have on this devastating disease.鈥 Professor Martin said.

The research grant is being administered by NHMRC, on behalf of the Australian Government Department of Health, through the MRFF Stem Cell Therapies Mission grant.

The Stem Cell Therapies Mission supports world-leading stem cell research that develops and delivers innovative, safe and effective stem cell medicines to improve health outcomes that are accessible to all Australians who need them.