This MRC New Investigator Research Grant was only possible due to my ERUK Fellowship Award. Support from Epilepsy Research UK has enabled me not only to apply for this grant, but to collaborate with a team in Italy to learn about key advanced molecular genetic techniques that can be implemented in our lab at the Institute of Neurology.
Dr Gabriele Lignani

ERUK Fellow Dr Gabriele Lignani is investigating the potential of gene therapy as a treatment for acquired hard-to-treat epilepsy. Earlier this year Dr Lignani was awarded funding from the prestigious Medical Research Council.

The New Investigator Research Grant, worth nearly £700,000, will be used to investigate the potential use of gene therapy in Dravet syndrome. This research project will build on Dr Lignani’s ongoing ERUK Fellowship research – GeneLoop, which is currently investigating the potential of gene therapy as a treatment for acquired intractable epilepsy.

Dravet syndrome is a severe and extremely rare but catastrophic neurological disorder affecting young children (approximately 1 in 19,000 people). Every day three or four children are diagnosed with Dravet syndrome worldwide, with symptoms including epilepsy, autism, movement disorders, and sleep disturbances. To date, the majority of therapies are ineffective or poorly tolerated and some medications can even exacerbate the problems.

Dr Gabriele Lignani

Funding leveraged

For every £1 invested, our researchers have leveraged a further £5.16 in funding

The importance of the initial ERUK funding cannot be over emphasised. As Dr Lignani says, “This MRC New Investigator Research Grant was only possible due to my ERUK Fellowship Award. Support from Epilepsy Research UK has enabled me not only to apply for this grant, but to collaborate with a team in Italy to learn about key advanced molecular genetic techniques that can be implemented in our lab at the Institute of Neurology. This further research grant is recognition of the high standard of ERUK-funded research.”

He continued, “This research will be useful not only to understand if a permanent general treatment for Dravet syndrome is achievable, but will also give insight into the potential of the techniques to cure other neurological conditions caused by similar mutations in different genes.”

Dr Lignani’s ERUK Fellowship officially began in 2018 but is already showing promising results. His team’s work thus far has focused on developing and testing their gene therapy tools, and they have found that this tool is able to subdue neurons during epileptic activity. The following stages of the fellowship will involve trialing these tools in models of acquired intractable epilepsy.

A massive WELL DONE to Dr Lignani from us all at ERUK!