METHODS OF REDUCING SERUM LEVELS OF FC-CONTAINING AGENTS USING FCRN ANTAGONISTS
Provided are novel methods of reducing the serum levels of Fc-containing agents (e.g., antibodies and immunoadhesins) in a subject. These methods generally comprise administering to the subject an effective amount of an isolated FcRn-antagonist that binds specifically to FcRn with increased affinity and reduced pH dependence relative to the native Fc region. The disclosed methods are particularly useful for treating antibody-mediated disorders (e.g. autoimmune diseases).
1 . A method of reducing the serum levels of an Fc-containing agent in a subject, the method comprising administering to the subject an effective amount of an isolated FcRn-antagonist comprising a variant Fc region, or FcRn-binding fragment thereof, wherein the Fc domains of the variant Fc region comprise the amino acids Y, T, E, K, F, and Y at EU positions 252, 254, 256, 433, 434, and 436 respectively, and wherein the FcRn-antagonist is administered to the subject in a dose of between about 0.2 and about 200 mg/kg.
2 . A method of reducing the serum levels of an Fc-containing agent in a subject, the method comprising administering to the subject an effective amount of an isolated FcRn-antagonist comprising a variant Fc region, or FcRn-binding fragment thereof, wherein the Fc domains of the variant Fc region comprise the amino acids Y, T, E, K, F, and Y at EU positions 252, 254, 256, 433, 434, and 436 respectively, and wherein the FcRn-antagonist is administered to the subject at least twice in 20 days.
3 - 6 . (canceled)
7 . A method of reducing the serum levels of an Fc-containing agent in a subject, the method comprising administering to the subject an effective amount of an isolated FcRn-antagonist comprising a variant Fc region, or FcRn-binding fragment thereof, wherein the Fc domains of the variant Fc region comprise the amino acids Y, T, E, K, F, and Y at EU positions 252, 254, 256, 433, 434, and 436 respectively, and wherein the FcRn-antagonist is administered to the subject at a frequency of once every 48 hours for four weeks.
8 - 15 . (canceled)
16 . The method of claim 1 , wherein the FcRn-antagonist does not comprise an antibody variable region.
17 . The method of claim 1 , wherein the FcRn-antagonist does not comprise a CH1 domain.
18 . The method of claim 1 , wherein the FcRn-antagonist does not comprise a free cysteine residue.
19 . The method of claim 1 , wherein the variant Fc region is an IgG Fc region.
20 . The method of claim 1 , wherein the variant Fc region is an IgG1 Fc region.
21 . The method of claim 1 , wherein the amino acid sequence of the Fc domains of the variant Fc region comprises the amino acid sequence set forth in SEQ ID NO:1, 2, or 3.
22 . The method of claim 1 , wherein the amino acid sequence of the Fc domains of the variant Fc region consists of the amino acid sequence set forth in SEQ ID NO:1.
23 . The method of claim 1 , wherein the FcRn-antagonist consists of a variant Fc region, wherein the amino acid sequence of the Fc domains of the variant Fc region consists of the amino acid sequence set forth in SEQ ID NO:1, 2, or 3.
24 . (canceled)
25 . (canceled)
26 . The method of claim 1 , wherein the Fc domains of the variant Fc region do not comprise an N-linked glycan at EU position 297.
27 . The method of claim 1 , wherein the FcRn-antagonist comprises a plurality of FcRn-antagonist molecules, wherein at least 50% of the plurality of FcRn-antagonist molecules comprise a variant Fc region, or FcRn-binding fragment thereof, comprising an afucosylated N-linked glycan at EU position 297.
28 . The method of claim 1 , wherein the FcRn-antagonist comprises a plurality of FcRn-antagonist molecules, wherein at least 50% of the plurality of FcRn-antagonist molecules comprise a variant Fc region or FcRn-binding fragment thereof, comprising an N-linked glycan having a bisecting GlcNac at EU position 297.
29 . The method of claim 1 , wherein the variant Fc region is linked to a half-life extender.
30 - 36 . (canceled)
37 . The method of claim 1 , wherein the subject has an antibody-mediated disease or disorder, and wherein administration of the FcRn-antagonist to the subject ameliorates the disease or disorder.
38 . The method of claim 37 , wherein the antibody-mediated disease or disorder is an autoimmune disease.
39 . (canceled)
40 . (canceled)
41 . The method of claim 38 , wherein the autoimmune disease is an autoimmune channelopathy.
42 . (canceled)
43 . The method of claim 37 , wherein the antibody-mediated disease or disorder is hyperglobulinemia.
44 - 50 . (canceled)
51 . The method of claim 1 , wherein the subject is a human or cynomolgus monkey.