Malin restoration as proof of concept for gene therapy for Lafora disease

Lafora disease is a fatal neurodegenerative childhood dementia caused by loss-of-function mutations in either the laforin or malin gene. The hallmark of the disease is the accumulation of abnormal glycogen aggregates known as Lafora bodies (LBs) in the brain and other tissues. These aggregates are responsible for the pathological features of the disease. As a monogenic disorder, Lafora disease is a good candidate for gene therapy-based approaches. However, most patients are diagnosed after the appearance of the first symptoms and thus when LBs are already present in the brain. In this context, it was not clear whether the restoration of a normal copy of the defective gene (either laforin or malin) would prove effective. Here we evaluated the effect of restoring malin in a malin-deficient mouse model of Lafora disease as a proof of concept for gene replacement therapy. To this end, we generated a malin-deficient mouse in which malin expression can be induced at a certain time. Our results reveal that malin restoration at an advanced stage of the disease arrests the accumulation of LBs in brain and muscle, induces the degradation of laforin and glycogen synthase bound to the aggregates, and ameliorates neuroinflammation. These results identify malin restoration as the first therapeutic strategy to show effectiveness when applied at advanced stages of Lafora disease. Lafora disease is a fatal childhood dementia caused by mutations in either laforin or malin genes. Duran et al. evaluated malin restoration as a proof of concept for a therapeutic approach for malin-deficient Lafora disease. They show that malin restoration is an effective treatment even when applied at an advanced stage of the disease.

Automated summary

Lafora disease is a fatal childhood dementia caused by mutations in either laforin or malin genes. Restoring malin at an advanced stage of the disease has shown to be an effective treatment.