COMBINATION THERAPY FOR TREATMENT OF IMMUNE DISORDERS
Methods and compositions are provided for the treatment of immune disorders, such as autoimmune diseases, or cancers, involving combination therapy with agents that inhibit the development or maintenance of Th17 cells. Treatment regimens are provided in which an antagonist of a pro-inflammatory cytokine is administered for a time sufficient to alleviate signs and symptoms of an acute phase flare-up of the autoimmune disease, or cancer, and treatment with an antagonist of IL-23 is continued for a longer time to prevent recurrence of the acute event. Antagonists of PGE2 and CD161 are also disclosed for use in treatment of autoimmune, inflammatory and proliferative disorders.
1 . A method of treating a subject having cancer or exhibiting a flare up of an autoimmune disease, comprising:
a) administration of an antagonist of IL-23 in a series of one or more doses over a first time interval; and
b) administration of antagonist of a cytokine selected from the group consisting of IL-1β, TNF-α, IL-17A, and IL-17F in a series of one or more doses over a second time interval.
2 . The method of claim 1 wherein the antagonist of IL-23 comprises:
a) an anti-IL-23p19 antibody or an antigen binding fragment thereof; or
b) an anti-IL-23R antibody or an antigen binding fragment thereof.
3 . (canceled)
4 . The method of claim 1 wherein the antagonist of a cytokine selected from the group consisting of IL-1β, TNF-α, IL-17A, and IL-17F comprises:
a) an antibody, or an antigen binding fragment thereof, that specifically binds to IL-1β, TNF-α, IL-17A, or IL-17F; or
b) an antibody, or an antigen binding fragment thereof, that specifically binds to a receptor of IL-1β, TNF-α, IL-17A, or IL-17F.
5 . (canceled)
6 . The method of claim 1 wherein the second time interval ends upon the resolution of at least one symptom of the flare-up of the autoimmune disease.
7 - 9 . (canceled)
10 . The method of claim 1 wherein the second time interval ends before the first time interval begins.
11 - 14 . (canceled)
15 . The method of claim 2 wherein the antibody or antigen binding fragment thereof is a humanized or fully human antibody or antigen binding fragment thereof.
16 . The method of claim 2 wherein the antibody or antigen binding fragment thereof is a fragment of a humanized or fully human antibody selected from the group consisting of a Fab, Fab′, Fab′-SH, Fv, scFv, F(ab′) 2 , and a diabody.
17 . The method of claim 2 wherein the antibody or antigen binding fragment thereof is PEGylated.
18 . The method of claim 2 wherein the antibody or antigen binding fragment thereof is a bispecific antibody or antigen binding fragment thereof.
19 . The method of claim 18 wherein the bispecific antibody binds to:
a) IL-23p19 or IL-23R; and
b) IL-1β, TNF-α, IL 7A, IL-17F or any of their receptors.
20 . (canceled)
21 . A pharmaceutical composition comprising:
a) an antibody, or antigen binding fragment thereof, that binds to IL-23p19 or IL-23R; and
b) an antibody, or antigen binding fragment thereof, that binds to IL-1β, TNF-α, IL-17A, IL-17F, or any of their receptors.
22 - 24 . (canceled)
25 . The method of claim 1 , wherein the subject has a disorder selected from the group consisting of cancer, arthritis, rheumatoid arthritis (RA), psoriasis, inflammatory bowel disease. Crohn's disease, ulcerative colitis, multiple sclerosis (MS), systemic lupus erythematosus (SLE), and type I diabetes.
26 - 27 . (canceled)
28 . A method of treating a subject having cancer or exhibiting a flare up of an autoimmune disease, comprising administering a binding composition derived from the antigen binding sites of antibodies, wherein the binding composition binds to IL-23R and CD161.
29 - 31 . (canceled)
32 . A composition for treatment of an autoimmune or proliferative disorder comprising two or more agents selected from the group consisting of an antagonist of IL-23, an antagonist of IL-1β, an antagonist of PGE2, an antagonist of IL-23 receptor, an antagonist of IL-1βreceptor, and an antagonist of a PGE2 receptor.
33 . (canceled)
34 . The composition of claim 32 wherein the composition comprises a bispecific antibody or antigen binding fragment thereof.
35 . A method of generating pathogenic Th17 cells in vitro comprising culturing T cells in vitro in the presence of two or more agents selected from the group consisting of IL-23, IL-1β, and PGE2.
36 . A method of screening for compounds for use in the treatment of disorders mediated by pathogenic Th17 cells comprising:
a) generating pathogenic Th17 cells by the method of claim 35 ;
b) exposing said cells to one or more potential therapeutic compounds; and
c) evaluating the effect of such compound(s) on said Th17 cells.
37 . A method of treating a subject having an autoimmune or proliferative disorder comprising:
administering to said subject a composition of claim 32 .
38 . (canceled)