“…Small molecules or monoclonal antibodies could be used to prevent NMO-IgG binding to AQP4 and to block the physiopathological cascade upstream (Verkman et al, 2011;Yu et al, 2011). Another strategy may deplete pathogenic antibodies by apheresis using dedicated immunoadsorption systems as previously described in myasthenia gravis (Zisimopoulou et al, 2008) and in various extra neurological disorders. However the value of this technique is less clear in disorders like MS (De Andres et al, 2000;Moldenhauer et al, 2005) where pathology is broader than a specific antibody.…”