FCRN antagonist molecules and methods of use thereof
By developing a novel FcRn antagonist molecule, specifically binds and inhibits the binding of IgG to FcRn, the problem of prolonging IgG half-life is solved, and the level of serum IgG antibodies is achieved rapidly, and the effect of treating autoimmune diseases and inflammatory diseases is achieved.
Patent Information
- Application Number
- CN202380082826.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Priority Date
- 2022-11-14
- Filing Date
- 2023-11-14
- Publication Date
- 2025-07-18
AI Technical Summary
In the prior art, the binding of FcRn to IgG leads to an extended half-life of IgG, which cannot effectively reduce the therapeutic effect of autoimmune diseases and inflammatory diseases. Antagonists are needed to prevent the binding of IgG to FcRn to regulate serum IgG levels.
A novel FcRn antagonist molecule was developed to reduce the serum IgG antibody level of subjects by specifically binding to FcRn and inhibiting the binding of IgG to FcRn, and to form a stable composition using the dimer domain of the variant Fc region, including specific amino acid sequences and glycan modifications.
Rapidly reduce subjects' serum IgG antibody levels, showing long-term stability, and are effective in the treatment of autoimmune and inflammatory diseases.
Smart Images

Figure BDA0005428489240000141 
Figure BDA0005428489240000142 
Figure BDA0005428489240000151
Abstract
Citation Information
Patent Citations
Methods and transformed mammalian lymphocytic cells for producing functional antigen-binding protein including chimeric immunoglobulin and fragments
US5807715A
Method of eliminating inhibitory / instability regions of mRNA
US5965726A
Method of eliminating inhibitory / instability regions from mRNA
US6174666B1
Method of eliminating inhibitory / instability regions of mRNA
US6291664B1
Method of eliminating inhibitory / instability regions of mRNA
US6414132B1