For US Healthcare Professionals
*While seronegative gMG is believed to be an autoimmune condition, its pathophysiology remains unclear.4
CD19 and CD20 are expressed at different stages of B cell development. CD19 appears early and remains present through much of the lifecycle, including on plasmablasts and some plasma cells that produce autoantibodies.2,8 CD20 appears later and is not present on these antibody-secreting cells.7,8
Global MG prevalence has more than doubled in the past 20 years, likely due to improvements in diagnosis, survival, and life expectancy9
gMG has a bimodal distribution, with a higher incidence in5
women between 30 to 50 years old
and men between 60 and 89 years old
AChR+, acetylcholine receptor positive; LRP4, low-density lipoprotein receptor-related protein 4; MuSK+, muscle-specific kinase positive.
1. Lazaridis K, Tzartos SJ. Front Neurol. 2020;11:596981.
2. Yi JS, Guptill JT, Stathopoulos P, Nowak RJ, O'Connor KC. Muscle Nerve. 2018;56(2):172-184.
3. Sun B, Ramberger M, O’Connor KC, et al. Nat Rev Neurol. 2020;16(9):481-492.
4. Fichtner ML, Jiang R, Bourke A, et al. Front Immunol. 2020;11.
5. Dresser L, Wlodarski R, Rezania K, Soliven B. J Clin Med. 2021;10:2235.
6. Evoli A, Palace J, Spagni G, et al. Neuromusc Disord. 2024;(44):104468.
7. Baker D, Marta M, Pryce G, et al. EBioMedicine. 2017;16:41-50.
8. Forsthuber TG, Cimbora DM, Ratchford JN, et al. Ther Adv Neurol Disord. 2018;11:1-13.
9. Park JY, Kim M, McCloskey C, Patterson KR, Meyers A. Poster presented at: American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM): October 2024 Savannah, GA.