“…On the other hand, AGA do not seem to increase significantly following ganglioside intramuscular administration in normal subjects [4], and the widespread use of gangliosides in our country during recent years has not been associated with an increasing incidence of GBS [Italian Consiglio Superiore di Sanità, unpublished data]. Thus, it is possible that exogenous gangliosides are immunogenic only in some sensitized subjects, as in the patient with chronic-progressive MS described by Knorr-Held et al [7], who developed an axonal GBS after therapeutic swine brain implantation, and in the present case, in view of an abnormal hypersensitivity to gangliosides, which may occur in active MS [6]. In our case, in view of the markedly prolonged DML and normal conduction velocities, motor nerve terminals may have been primarily involved since, at this level, the blood-nerve barrier is more permeable to antibody penetration, and binding with anti-GM1 and GD1b antibodies is possible in GBS [5].…”