US2016222111A1PendingUtilityA1
Fc receptor binding proteins
Est. expiryApr 25, 2028(~1.8 yrs left)· nominal 20-yr term from priority
Inventors:Christopher TenhoorArumugam MuruganandamRobert Charles LadnerClive WoodAlan J. BitontiJames McgivneyKevin McdonnellLiming LiuJennifer A. DumontAaron SatoMalini Viswanathan
C07K 2317/21C07K 16/28C07K 2317/76C07K 16/283A61K 39/395A61K 2039/505C07K 2317/92C12N 15/09C07K 2317/33G01N 2333/70535C07K 2317/34A61K 49/16C07K 2317/565C07K 2317/55G01N 33/68A61K 49/0058C07K 2317/20G01N 33/6854C07K 2317/56A61P 37/00A61K 51/1027
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Claims
Abstract
This disclosure provides, inter alia, proteins that bind to FcRn, e.g., immunoglobulins that inhibit FcRn with high affinity and selectivity. The FcRn-binding proteins can be used to treat a variety of disorders including autoimmune disorders.
Claims
exact text as granted — not AI-modified1 - 67 . (canceled)
68 . A method of modulating an FcRn activity, the method comprising:
contacting FcRn with an antibody that binds human FcRn, thereby modulating the activity of the FcRn, wherein the antibody comprises a heavy chain (HC) immunoglobulin variable domain sequence and a light chain (LC) immunoglobulin variable domain sequence; and wherein the HC comprises:
a HC CDR1 comprising the amino acid sequence EYAMG (SEQ ID NO:144) or VYAMG (SEQ ID NO:156),
a HC CDR2 comprising the amino acid sequence SIGSSGGQTKYADSVKG (SEQ ID NO:145) or SIGSSGGPTKYADSVKG (SEQ ID NO:157), and
a HC CDR3 comprising the amino acid sequence LSTGELY (SEQ ID NO:146), LSIRELV (SEQ ID NO:158), LSIVDSY (SEQ ID NO:164), LSLGDSY (SEQ ID NO:170), or, LAIGDSY (SEQ ID NO:176); and
the LC comprises:
a LC CDR1 comprising the amino acid sequence TGTGSDVGSYNLVS (SEQ ID NO:141),
a LC CDR2 comprising the amino acid sequence GDSQRPS (SEQ ID NO:142), and
a LC CDR3 comprising the amino acid sequence CSYAGSGIYV (SEQ ID NO:143).
69 - 110 . (canceled)
111 . The method of claim 68 , wherein the FcRn is in a human subject.
112 . The method of claim 68 , wherein the antibody prevents binding of the FcRn to an endogenous Ig.
113 . The method of claim 68 , wherein the antibody prevents binding of the FcRn to a therapeutic antibody.
114 . The method of claim 68 , wherein the binding between FcRn and the antibody occurs in an epithelial cell endosome.
115 . The method of claim 68 , wherein the binding between FcRn and the antibody occurs in an endothelial cell endosome.
116 . The method of claim 68 , wherein the binding between FcRn and the antibody occurs on the cell surface.Cited by (0)
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