Experimental Neurobiology 2019; 28(6): 720-726
Published online December 31, 2019
© The Korean Society for Brain and Neural Sciences
Young Gi Min1, Canaria Park2, Young-Nam Kwon1,3, Je-Young Shin1, Jung-Joon Sung1,2 and Yoon-Ho Hong2,3*
1Department of Neurology, Seoul National University Hospital, Seoul 03080, 2Seoul National University College of Medicine and Neuroscience Research Institute, Seoul National University Medical Research Council, Seoul 03080, 3Department of Neurology, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul 07061, Korea
Correspondence to: *To whom correspondence should be addressed.
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Myasthenia gravis (MG) is an autoimmune neuromuscular junction disorders mediated by various autoantibodies. Although most patients with MG require chronic immunosuppressive treatment to control disease activity, appropriate surveillance biomarkers that monitor disease activity or potential toxicity of immunosuppressants are yet to be developed. Herein, we investigated quantitative distribution of peripheral blood B cell subsets and transcriptional profiles of memory B cells (CD19+ CD27+) in several subgroups of MG patients classified according to the Myasthenia Gravis Foundation of America (MGFA) Clinical Classification. This study suggests potential immunologic B-cell markers that may guide treatment decision in future clinical settings.