Iosif Xidakis, Dimitrios Parisis, Theodoros Karapanayiotides, Nikolaos Grigoriadis, John Elloul, Vasiliki Kostadima, Dimitra Papadimitriou, Marianthi Breza, Elisabeth Chroni, Christos Bakirtzis, Georgios Koutsis, Katerina Karagiorgou, Sygkliti-Henrietta Pelidou, Anastasios Orologas, Ioannis Markakis, Paraskevi Zisimopoulou, Konstantinos Notas, C. Kilidireas, Ioannis Nikolaidis, Maria Anagnostouli, Socrates J. Tzartos, Maria-Eleftheria Evangelopoulos, Thomas Maris, Dimitrios Tzanetakos, and John Tzartos
IgG antibodies to myelin oligodendrocyte glycoprotein (MOG) detected by cell based assays (CBA) have been identified in a constantly expanding spectrum of CNS demyelinating disorders. However, a universally accepted CBA has not been adopted yet. We aimed to analyze the clinical and radiological features of patients with anti-MOG IgG1-antibodies detected with a live-cell CBA and to compare the three most popular MOG-CBAs. We screened sera from 1300 Greek patients (including 426 patients referred by our 8 clinics) suspected for anti-MOG syndrome, and 120 controls with the live-cell MOG-CBA for IgG1-antibodies. 41 patients, versus 0 controls were seropositive. Clinical, serological and radiological data were available and analyzed for the 21 seropositive patients out of the 426 patients of our clinics. Their phenotypes were: 8 optic neuritis, 3 myelitis, 3 neuromyelitis optica, 2 encephalomyelitis, 2 autoimmune encephalitis and 3 atypical MS. We then retested all sera of our 426 patients with the other two most popular MOG-CBAs for total IgG (a live-cell and a commercial fixed-cell CBAs). Seven IgG1-seropositive patients were seronegative for one or both IgG-CBAs. Yet, all 21 patients had clinical and radiological findings previously described in MOG-antibody associated demyelination disease supporting the high specificity of the IgG1-CBA. In addition, all IgG1-CBA-negative sera were also negative by the IgG-CBAs. Also, all controls were negative by all three assays, except one serum found positive by the live IgG-CBA. Overall, our findings support the wide spectrum of anti-MOG associated demyelinating disorders and the superiority of the MOG-IgG1 CBA over other MOG-CBAs.