› Alliance MyoNeuRALP
Led by Prof. Laurent SCHAEFFER, this pole of excellence aims at developing multi-scale strategies to understand neuromuscular diseases, identify new therapeutic targets and bring out new treatments and innovative biomarkers.
The MyoNeurALP alliance has been labeled “strategic pole” by the AFM-Téléthon since 2017.
The alliance brings together the main research teams in Rhone Alpes Auvergne involved in research on neuromuscular disosrders, the local players of the Regional Reference Center for Rare Neuromuscular Diseases and the 4 University Hospital Research Centers involved in the study of the neuromuscular system and its pathologies:
- Lyon – 12 INMG teams: L. Beccari, B. Chazaud, J. Courchet, V. Gache, A. Giglia Mari, V. Jacquemond, F. Le Grand, P. Lomonte, C. Marcelle, R. Mounier, H. Puccio, L. Schaeffer
- Clermont Ferrand – 3 teams of the GReD : C. Guillot, C. Jagla, V. Mirouse
- Grenoble – 1 team of the GIN : I. Marty
- Saint Etienne – 1 team of the LIBM: D. Freyssenet, 1 INMG team: J.C. Antoine
This network has been labeled by the Ministry of Health (Investissement d’avenir) and INSERM to bring neurology closer to immunology and develop innovative approaches for inflammatory diseases of the nervous and neuromuscular system
› RHU SMART
Spinal muscular atrophy caused by impairment of the SMN (survival of motor neurons) gene induces the death of neurons that control the activity of skeletal muscles. Currently about 1500 patients live in France with this disease. In its most severe form, it causes the death of most children before the age of 2 years. Revolutionary treatments recently developed by Roche, Novartis and Biogen have increased the life expectancy of children but have created a new clinical form of the disease which is crucial to characterize in order to allow good management of treated patients and consider future clinical trials to address functional deficits that persist despite treatment. Muscular atrophy is a major component of these deficiencies.
The RHU SMART (SMA Muscle Atrophy Remediative Therapy), led by Pr Laurent Schaeffer and endowed with funding of 9.4 million euros, has two main objectives:
– Describe the pathology of treated patients and identify relevant biomarkers through a multicenter and international natural history study.
– Develop a process for screening molecules to allow the emergence of treatments for muscle atrophy. SMART brings together 6 laboratory teams (B. Chazaud, J. Courchet, V. Gache, V. Jacquemond, R. Mounier, L. Schaeffer), the teams of D. Freyssenet and G. Millet from the LIBM in Saint-Etienne and that of F. Charbonnier from the University of Paris, 2 local biotechs (Cytoo, EnyoPharma) and 2 large industrial groups (Roche and Sysnav).
Our ambition for the SMART project is to initiate the creation of a clinical investigation platform for neuromuscular diseases that would combine academic research, therapeutic trials and access to innovative molecules in the field of neuromuscular diseases.
› The national network of health of the neuromuscular diseases (FILNEMUS): the active part played by the actors of the network MyoNeuRALP in the setting up of the sector illustrates the national recognition of our expertise in research, diagnosis, databases and therapeutic tests
› RESOCANAUX: this consortium aims to address, through collaborative research, the clinical, genetic, physiopathological and therapeutic aspects of neuromuscular diseases involving ion channels.
› A dense network of collaborations:
- Institute of Myology
- ISTEM Stem Cell Institute
- Atlantic Gene therapy
- Timone Hospital, Marseille
- Creteil Hospital / Veterinary School of Maisons-Alfort
- IGBMC Strasbourg
› Lyon-Ottawa partnership: Join Institute for Neuromuscular research
L. Schaeffer is the coordinator of the LIA JIN (Join Institute for Neuromuscular research). The CNMD is one of the largest institutes in the world dedicated to research on the neuromuscular system. It unites basic and clinical researchers from across the University of Ottawa and affiliated hospitals to advance our understanding of the underlying pathological mechanisms and identify novel treatment strategies for neuromuscular disease patients. Like our laboratory, the CNMD (Centre for Neuromuscular Disease) hosts muscle biology teams, neurobiologists and specialists of epigenetic regulation in muscle and neuronal cells forming a community of researchers and clinicians with expertise at all levels of the neuromuscular system with scientific expertise ranging from molecular biology, cell biology, electrophysiology to integrated human physiology. This partnership has been endorsed by CNRS with the label “Laboratoire International Associé”. The partnership benefits of an annual funding from Lyon university and CNRS to fund collaborative research programs and exchanges between the teams of the two laboratory.