Uses of IL-15 antagonists for the treatment of autoimmune and inflammatory diseases
The present relates to interleukin 15 (IL-15) antagonists and uses thereof, in particular for the treatment of autoimmune diseases and inflammatory diseases. In particular, the present invention relates to an IL-15 mutant polypeptide having the amino acid sequence as set forth in SEQ ID NO:1 wherein the leucine residue at position 45 is substituted by an aspartic acid residue, the asparagines residue at position 65 is substituted by a lysine residue and the leucine residue at position 69 is substituted by an arginine residue.
1. A method of treating an inflammatory or autoimmune disease associated with IL-15 in a patient in need thereof, comprising administering to said patient a therapeutically effective amount of an IL-15 antagonist selected from:
an IL-15 mutant polypeptide which amino acid sequence is identical to the sequence in SEQ ID NO:1 except the leucine residue at position 45 is substituted by an aspartic acid residue, the asparagine residue at position 65 is substituted by a lysine residue, and the leucine residue at position 69 is substituted by an arginine residue; and
a fusion protein comprising the IL-15 mutant polypeptide fused to a heterologous polypeptide, or a dimer thereof.
2. The method according to claim 1 wherein the inflammatory or autoimmune disease is selected from the group consisting of a rheumatic disease, systemic lupus erythematosus, Sjogren's syndrome, scleroderma, mixed connective tissue disease, dermatomyositis, polymyositis, Reiter's syndrome or Behcet's disease, diabetes, an autoimmune disease of the thyroid, an autoimmune disease of the central nervous system, phemphigus, psoriasis, and inflammatory bowel disease.
3. The method of claim 2 , wherein the rheumatic disease is rheumatoid arthritis.
4. The method of claim 2 , wherein the autoimmune disease of the thyroid is Hashimoto's thyroiditis or Graves' Disease.
5. The method of claim 2 , wherein the autoimmune disease of the central nervous system is selected from the group consisting of multiple sclerosis, myasthenia gravis and encephalomyelitis.
6. The method of claim 2 , wherein the said phemphigus is selected from the group consisting of phemphigus vulgaris, phemphigus vegetans, phemphigus foliaceus, Senear-Usher syndrome and Brazilian phemphigus.
7. The method of claim 2 , wherein the inflammatory bowel disease is ulcerative colitis or Crohn's Disease.
8. The method of claim 1 , wherein the heterologous polypeptide is an immunoglobulin constant domain.
9. The method of claim 8 , wherein the immunoglobulin constant domain is obtained from an immunoglobulin selected from the group consisting of IgG-1, IgG-2, IgG-3, IgG-4, IgA, IgE, IgD and IgM.
10. The method of claim 8 , wherein the immunoglobulin constant domain is a Fc region.
11. The method of claim 8 , wherein the IL-15 mutant polypeptide and the immunoglobulin constant domain are linked by a linker.
12. The method of claim 11 , wherein the linker has 4; 5; 6; 7; 8; 9; 10; 11; 12; 13; 14; 15; 16; 17; 18; 19; 20; 21; 22; 23; 24; 25; 26; 27; 28; 29; or 30 amino acid residues.
13. The method of claim 11 , wherein the linker is selected from the group consisting of SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14 and SEQ ID NO:15.
14. The method of claim 1 , wherein the IL-15 mutant polypeptide has an amino acid sequence selected from the group consisting of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:7, SEQ ID NO:8 and SEQ ID NO:9.
15. A method of treating inflammation associated with IL-15 in a transplant patient in need thereof, comprising administering to said patient a therapeutically effective amount of an IL-15 antagonist selected from:
an IL-15 mutant polypeptide which amino acid sequence is identical to the sequence in SEQ ID NO:1 except the leucine residue at position 45 is substituted by an aspartic acid residue, the asparagine residue at position 65 is substituted by a lysine residue, and the leucine residue at position 69 is substituted by an arginine residue; and
a fusion protein comprising the IL-15 mutant polypeptide fused to a heterologous polypeptide, or a dimer thereof.
16. The method of claim 15 , wherein the transplant patient has graft versus host disease.