1. Academic Validation
  2. The Fusion Protein MuSK-Fc Functions as a Decoy to Block the Binding of Anti-MuSK Antibodies to MuSK

The Fusion Protein MuSK-Fc Functions as a Decoy to Block the Binding of Anti-MuSK Antibodies to MuSK

  • Scand J Immunol. 2025 May;101(5):e70033. doi: 10.1111/sji.70033.
Akiyuki Uzawa 1 Hiroyuki Akamine 1 2 Manato Yasuda 1 Hideo Handa 1 Etsuko Ogaya 1 Kentaro Kurumada 1 Yosuke Onishi 1 Satoshi Kuwabara 1 3
Affiliations

Affiliations

  • 1 Department of Neurology, Graduate School of Medicine, Chiba University, Japan.
  • 2 Department of Cardiovascular Medicine, Nephrology, and Neurology, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
  • 3 Research Institute of Disaster Medicine, Chiba University, Japan.
Abstract

Muscle-specific tyrosine kinase antibody-positive myasthenia gravis (MuSKMG) is a rare subtype of MG that is often more refractory to immune treatment than acetylcholine receptor (AChR) antibody-positive MG. Therefore, novel therapeutic strategies are needed. We previously developed AChR-Fc, an Fc fusion protein that neutralises pathogenic autoantibodies and suppresses pathogenic B cells while preserving normal immunity, as a potential treatment for AChR antibody-positive MG. Subsequently, we conducted preliminary experiments on MuSK-Fc, a fusion protein targeting MuSKMG, using patient serum samples. This study examined whether MuSK-Fc binds to MuSK antibodies and inhibits MuSK antibody binding to MuSK. We found that MuSK-Fc specifically binds to MuSK antibodies and prevents their interaction with MuSK. These findings indicate that MuSK-Fc may neutralise pathogenic antibodies and suppress disease activity in MuSKMG.

Keywords

fusion protein; muscle‐specific tyrosine kinase; myasthenia gravis; neutralisation; novel treatment.

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