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ABSTRACT: Background and objectives
Myasthenia gravis (MG) is a T cell-dependent, B cell-mediated autoimmune disease targeting the acetylcholine receptor (AChR) and other proteins of the neuromuscular junction postsynaptic membrane. Production of pathogenic autoantibodies results from B cell activation and expansion of antibody-secreting cells, including plasma cells, whose differentiation and survival are reliant on the TNF family cytokines APRIL and BAFF. Povetacicept (ALPN-303; TACI vTD-Fc) is an Fc fusion protein of an engineered TACI domain with significantly more potent dual inhibition of APRIL and BAFF than wild-type (WT) TACI-Fc (e.g., telitacicept).Methods
In this study, the activity of povetacicept was evaluated in the mouse experimental autoimmune MG (EAMG) model, compared
SUBMITTER: Rinaldi E
PROVIDER: S-EPMC12179661 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature