METHODS OF TREATMENT USING ILT7 BINDING PROTEINS
The present disclosure is related to methods of treating autoimmune disorders in a subject comprising administering immunoglobulin-like transcript 7 (ILT7) binding proteins to a subject having elevated type I interferon gene signature (IFNGS). The present disclosure also relates to methods of reducing pDCs in tissues comprising administering an ILT7-binding protein to a subject in need thereof.
1 . A method for reducing a type I interferon gene signature (IFNGS) in a subject in need thereof, the method comprising administering to the subject a pharmaceutically effective amount of an immunoglobulin-like transcript 7 (ILT7)-binding protein, wherein the ILT7 binding protein is administered to the subject when the type I IFNGS is elevated in the subject relative to the type I IFNGS in a normal subject.
2 . The method of claim 1 , wherein the type I IFNGS is measured in a test biological sample taken from the subject, and wherein the test biological sample is selected from the group consisting of blood, sputum, saliva, skin biopsy, kidney cells, lung cells, liver cells, heart cells, brain cells, nervous tissue, thyroid cells, eye cells, skeletal muscle cells, cartilage, bone tissue, and cultured cells.
3 . The method of claim 2 , wherein the test biological sample is blood, the skin biopsy.
4 . The method of claim 2 , wherein the type I IFNGS is elevated by at least about 4-fold in the test biological sample relative to the type I IFNGS level of the normal subject or a baseline level of a test biological sample of the subject in need thereof as determined by evaluating an mRNA level of a type I interferon gene.
5 . (canceled)
6 . The method of claim 1 , wherein the type I IFNGS is determined by a method comprising determining mRNA levels of at least two genes selected from the group consisting of SPATS2L, EPSTI1, HERC5, IFI27, IFI44, IFI44L, IFI6, IFIT1, IFIT3, ISG15, LAMP3, LY6E, MX1, OAS1, OAS2, OAS3, PLSCR1, RSAD2, RTP4, SIGLEC1, and USP18.
7 . The method according to claim 6 , wherein the type I IFNGS is determined by a method comprising determining mRNA levels all of SPATS2L, EPSTI1, HERC5, IFI27, IFI44, IFI44L, IFI6, IFIT1, IFIT3, ISG15, LAMP3, LY6E, MX1, OAS1, OAS2, OAS3, PLSCR1, RSAD2, RTP4, SIGLEC1, and USP18.
8 . (canceled)
9 . (canceled)
10 . The method of claim 1 , wherein the administering is effective in reducing a level of:
i. plasmacytoid dendritic cells (pDCs);
ii. type I IFNGS; and/or
iii. the pDCs and the type I IFNGS.
11 . (canceled)
12 . (canceled)
13 . The method of claim 1 , wherein the subject in need has an autoimmune disease.
14 . The method of claim 13 , wherein the autoimmune disease is selected from the group consisting of systemic lupus erythematosus (SLE), lupus nephritis, cutaneous lupus erythematosus (CLE), Sjögren's syndrome, dermatomyositis, inclusion body myositis, juvenile myositis, polymyositis, systemic sclerosis, diabetes, Hashimoto's disease, autoimmune adrenal insufficiency, anemia, multiple sclerosis, rheumatic carditis, psoriasis, arthritis, inflammation, chronic rheumatism, vitiligo, alopecia areata, hidradenitis suppurativa, celiac disease, graft versus host disease (GVHD), myocardial infarction, and a Type-1 interferonopathy.
15 . The method of claim 14 , wherein the autoimmune disease is Sjögren's syndrome, dermatomyositis, vitiligo, polymyositis, systemic sclerosis, hidradenitis suppurativa, SLE or CLE.
16 .- 21 . (canceled)
22 . The method of claim 1 , wherein the ILT7-binding protein is an antibody comprising heavy chain Complementarity-Determining Regions (HCDRs) HCDR1, HDR2, HCDR3, and light chain Complementarity Determining Regions (LCDRs) LCDR1, LCDR2, and LCDR3 comprising the amino acid sequences of SEQ ID NOs: 3, 4, 5, 6, 7, and 8, respectively.
23 . The method of claim 22 , wherein the ILT7 binding protein is an antibody comprising a variable heavy chain (VH) that is at least 85%, identical to SEQ ID NO:1 and/or a variable light chain (VL) that is at least 85% identical to SEQ ID NO:2.
24 . The method of claim 22 , wherein the ILT7-binding protein is an antibody comprising a heavy chain variable region (VH) of SEQ ID NO:1 and a light chain variable region (VL) of SEQ ID NO:2.
25 . The method of claim 1 , wherein the ILT7-binding protein is an antibody that is afucosylated.
26 . The method of claim 1 , wherein the pharmaceutically effective amount ranges from about 0.1 mg to about 1000 mg.
27 . The method of claim 26 , wherein the pharmaceutically effective amount is about 1 mg, about 5 mg, about 15 mg, about 50 mg, about 100 mg, or about 150 mg.
28 . (canceled)
29 . The method of claim 10 , comprising the reduced level of type I IFNGS, wherein the reduction is at least about 50% as compared to the level prior to the administration of the ILT7-binding protein.
30 .- 43 . (canceled)
44 . A method of treating an autoimmune disorder in a subject in need thereof, the method comprising administering to the subject a pharmaceutically effective amount of an immunoglobulin-like transcript 7 (ILT7)-binding protein, wherein the pharmaceutically effective amount of the ILT7-binding protein is about 1 mg, about 5 mg, about 15 mg, about 50 mg, about 100 mg, or about 150 mg.
45 . The method of claim 44 , wherein the pharmaceutically effective amount of the ILT7-binding protein is about 50 mg.
46 . The method of claim 44 , wherein the pharmaceutically effective amount of the ILT7-binding protein is about 150 mg.
47 . The method of claim 44 , wherein the autoimmune disorder is selected from the group consisting of: systemic lupus erythematosus (SLE), lupus nephritis, cutaneous lupus erythematosus (CLE), Sjögren's syndrome, dermatomyositis, inclusion body myositis, juvenile myositis, polymyositis, systemic sclerosis, diabetes, Hashimoto's disease, autoimmune adrenal insufficiency, anemia, multiple sclerosis, rheumatic carditis, psoriasis, arthritis, inflammation, chronic rheumatism, vitiligo, alopecia areata, hidradenitis suppurativa, celiac disease, graft versus host disease (GVHD), myocardial infarction, and a Type-1 interferonopathy.
48 .- 65 . (canceled)
66 . A method of treating an autoimmune disorder, the method comprising administering an effective amount of an ILT7 binding protein to a subject in need thereof, wherein the administering is effective in treating the autoimmune disorder as determined by detecting in a sample of the subject:
i. fewer plasmacytoid dendritic cells (pDCs) compared to a sample of the subject before the administering; or
ii. reduced mRNA expression from a gene selected from the group consisting of: SPATS2L, EPSTI1, HERC5, IFI27, IFI44, IFI44L, IFI6, IFIT1, IFIT3, ISG15, LAMP3, LY6E, MX1, OAS1, OAS2, OAS3, PLSCR1, RSAD2, RTP4, SIGLEC1, and USP18,
compared to the mRNA expression level of the gene in a sample of the subject before the administering.
67 . The method of claim 66 , wherein the ILT7 binding protein is an antibody.
68 . The method of claim 67 , wherein the antibody comprises heavy chain Complementarity-Determining Regions (HCDRs) HCDR1, HDR2, HCDR3, and light chain Complementarity Determining Regions (LCDRs) LCDR1, LCDR2, and LCDR3 comprising the amino acid sequences of SEQ ID NOs: 3, 4, 5, 6, 7, and 8, respectively.
69 . The method of claim 68 , wherein the antibody comprises a variable heavy chain (VH) that is at least 85% identical to SEQ ID NO:1 and/or a variable light chain (VL) that is at least 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to SEQ ID NO:2.
70 . The method of claim 69 , wherein the VH comprises the polypeptide of SEQ ID NO:1, and wherein the VL comprises the polypeptide of SEQ ID NO: 2.
71 . The method of claim 66 , wherein the autoimmune disorder is selected from the group consisting of: systemic lupus erythematosus (SLE), lupus nephritis, cutaneous lupus erythematosus (CLE), Sjögren's syndrome, dermatomyositis, inclusion body myositis, juvenile myositis, polymyositis, systemic sclerosis, diabetes, Hashimoto's disease, autoimmune adrenal insufficiency, anemia, multiple sclerosis, rheumatic carditis, psoriasis, arthritis, inflammation, chronic rheumatism, vitiligo, alopecia areata, hidradenitis suppurativa, celiac disease, graft versus host disease (GVHD), myocardial infarction, and a Type-1 interferonopathy.